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<!--
|
||
UID=56429
|
||
ConceptID=C0162429
|
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Malnutrition</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>56429</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0162429</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Malnourishment; Malnourishments; Nutritional Deficiencies; Nutritional Deficiency; Undernutrition</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Undernutrition (65404009); Undernutrition syndrome (65404009); Undernourished (248325000); Malnourished (248325000); Underfed (248325000); Malnutrition (2492009)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0004395">HP:0004395</a></td></tr>
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<div class="portlet mgSection" id="ID_100">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">A deficiency in the intake of energy and nutrients. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0162429[DISCUI]&test_type=Clinical&redirect=true" ref="ncbi_uid=56429">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Malnutrition</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/3828" ref="tree=MeSH" title="MedGen record for Disorder of digestive system">Disorder of digestive system</a></span><ul><li><span class="TLline"><a href="/medgen/78584" ref="tree=MeSH" title="MedGen record for Abnormality of the digestive system">Abnormality of the digestive system</a></span><ul><li><span class="TLline"><a href="/medgen/927601" ref="tree=MeSH" title="MedGen record for Abnormality of digestive system physiology">Abnormality of digestive system physiology</a></span><ul><li><span class="TLline"><a href="/medgen/488929" ref="tree=MeSH" title="MedGen record for Abdominal symptom">Abdominal symptom</a></span><ul><li><span class="matched_ds">Malnutrition</span><ul><li><span class="TLline"><a href="/medgen/4169" ref="tree=MeSH" title="MedGen record for Deficiency Disease">Deficiency Disease</a></span><ul><li><span class="TLline"><a href="/medgen/91216" ref="tree=MeSH" title="MedGen record for Avitaminosis">Avitaminosis</a></span><ul><li><span class="TLline"><a href="/medgen/2093" ref="tree=MeSH" title="MedGen record for Decreased circulating vitamin C concentration">Decreased circulating vitamin C concentration</a></span></li><li><span class="TLline"><a href="/medgen/12114" ref="tree=MeSH" title="MedGen record for Decreased circulating vitamin D concentration">Decreased circulating vitamin D concentration</a></span></li><li><span class="TLline"><a href="/medgen/22668" ref="tree=MeSH" title="MedGen record for Vitamin A deficiency">Vitamin A deficiency</a></span></li><li><span class="TLline"><a href="/medgen/22669" ref="tree=MeSH" title="MedGen record for Vitamin B deficiency">Vitamin B deficiency</a></span></li><li><span class="TLline"><a href="/medgen/21881" ref="tree=MeSH" title="MedGen record for Vitamin E deficiency">Vitamin E deficiency</a></span></li><li><span class="TLline"><a href="/medgen/22672" ref="tree=MeSH" title="MedGen record for Vitamin K deficiency">Vitamin K deficiency</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/52602" ref="tree=MeSH" title="MedGen record for Enzootic Ataxia">Enzootic Ataxia</a></span></li><li><span class="TLline"><a href="/medgen/44244" ref="tree=MeSH" title="MedGen record for Magnesium deficiency">Magnesium deficiency</a></span></li><li><span class="TLline"><a href="/medgen/10874" ref="tree=MeSH" title="MedGen record for Potassium deficiency">Potassium deficiency</a></span></li><li><span class="TLline"><a href="/medgen/18705" ref="tree=MeSH" title="MedGen record for Protein Deficiency">Protein Deficiency</a></span><ul><li><span class="TLline"><a href="/medgen/19521" ref="tree=MeSH" title="MedGen record for Protein-energy malnutrition">Protein-energy malnutrition</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/266200" ref="tree=MeSH" title="MedGen record for Disorder of fetal nutrition">Disorder of fetal nutrition</a></span></li><li><span class="TLline"><a href="/medgen/167819" ref="tree=MeSH" title="MedGen record for Refeeding syndrome">Refeeding syndrome</a></span></li><li><span class="TLline"><a href="/medgen/875809" ref="tree=MeSH" title="MedGen record for Severe Acute Malnutrition">Severe Acute Malnutrition</a></span><ul><li><span class="TLline"><a href="/medgen/7233" ref="tree=MeSH" title="MedGen record for Kwashiorkor">Kwashiorkor</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/20944" ref="tree=MeSH" title="MedGen record for Starvation">Starvation</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
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</div>
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<div class="portlet mgSection" id="ID_112">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_42105"><div><strong>Hereditary fructosuria</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>42105</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0016751</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Following dietary exposure to fructose, sucrose, or sorbitol, untreated hereditary fructose intolerance (HFI) is characterized by metabolic disturbances (hypoglycemia, lactic acidemia, hypophosphatemia, hyperuricemia, hypermagnesemia, hyperalaninemia) and clinical findings (nausea, vomiting, and abdominal distress; chronic growth restriction / failure to thrive). While untreated HFI typically first manifested when fructose- and sucrose-containing foods were introduced in the course of weaning young infants from breast milk, it is now presenting earlier, due to the addition of fructose-containing nutrients in infant formulas. If the infant ingests large quantities of fructose, the infant may acutely develop lethargy, seizures, and/or progressive coma. Untreated HFI may result in renal and hepatic failure. If identified and treated before permanent organ injury occurs, individuals with HFI can experience a normal quality of life and life expectancy.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/42105">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_36311"><div><strong>Recessive dystrophic epidermolysis bullosa</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>36311</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0079474</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Dystrophic epidermolysis bullosa (DEB) is a genetic skin disorder affecting skin and nails that usually presents at birth. DEB is divided into two major types depending on inheritance pattern: recessive dystrophic epidermolysis bullosa (RDEB) and dominant dystrophic epidermolysis bullosa (DDEB). Each type is further divided into multiple clinical subtypes. Absence of a known family history of DEB does not preclude the diagnosis. Clinical findings in severe generalized RDEB include skin fragility manifest by blistering with minimal trauma that heals with milia and scarring. Blistering and erosions affecting the whole body may be present in the neonatal period. Oral involvement may lead to mouth blistering, fusion of the tongue to the floor of the mouth, and progressive diminution of the size of the oral cavity. Esophageal erosions can lead to webs and strictures that can cause severe dysphagia. Consequently, malnutrition and vitamin and mineral deficiency may lead to growth restriction in young children. Corneal erosions can lead to scarring and loss of vision. Blistering of the hands and feet followed by scarring fuses the digits into "mitten" hands and feet, with contractures and pseudosyndactyly. The lifetime risk of aggressive squamous cell carcinoma is higher than 90%. In contrast, the blistering in the less severe forms of RDEB may be localized to hands, feet, knees, and elbows with or without involvement of flexural areas and the trunk, and without the mutilating scarring seen in severe generalized RDEB. In DDEB, blistering is often mild and limited to hands, feet, knees, and elbows, but nonetheless heals with scarring. Dystrophic nails, especially toenails, are common and may be the only manifestation of DDEB.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/36311">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_75704"><div><strong>Lysinuric protein intolerance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75704</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information."><span class="highlight" style="background-color:">C0268647</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Lysinuric protein intolerance (LPI) typically presents after an infant is weaned from breast milk or formula; variable findings include recurrent vomiting and episodes of diarrhea, episodes of stupor and coma after a protein-rich meal, poor feeding, aversion to protein-rich food, failure to thrive, hepatosplenomegaly, and muscular hypotonia. Over time, findings include: poor growth, osteoporosis, involvement of the lungs (progressive interstitial changes, pulmonary alveolar proteinosis) and of the kidneys (progressive glomerular and proximal tubular disease), hematologic abnormalities (normochromic or hypochromic anemia, leukopenia, thrombocytopenia, erythroblastophagocytosis in the bone marrow aspirate), and a clinical presentation resembling the hemophagocytic lymphohistiocytosis/macrophagic activation syndrome. Hypercholesterolemia, hypertriglyceridemia, and acute pancreatitis can also be seen.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75704">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_137954"><div><strong>Congenital microvillous atrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>137954</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0341306</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Diarrhea-2 with microvillus atrophy, with or without cholestasis (DIAR2) is characterized by onset of intractable life-threatening watery diarrhea during infancy. Two forms are recognized: early-onset microvillus inclusion disease (MVID) with diarrhea beginning in the neonatal period, and late-onset, with first symptoms appearing after 3 or 4 months of life. Definite diagnosis is made by transmission electron microscopy demonstrating shortening or absence of apical microvilli with pathognomonic microvillus inclusions in mature enterocytes and peripheral accumulation of periodic acid-Schiff (PAS)-positive granules or vesicles in immature enterocytes (Muller et al., 2008). The natural course of MVID is often fatal, but partial or total weaning from parenteral nutrition has been described. For a discussion of genetic heterogeneity of diarrhea, see DIAR1 (214700).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/137954">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_208651"><div><strong>Chylomicron retention disease</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>208651</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0795956</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Chylomicron retention disease (CMRD), characterized by the inability to secrete chylomicrons from the enterocytes following the ingestion of fat, typically presents in infancy with failure to thrive, diarrhea, vomiting, abdominal distention, and malabsorption of fat. This leads to steatorrhea – the severity of which relates to the fat content of the diet – and in some cases, hepatomegaly. Organ systems outside of the gastrointestinal tract may also be affected (often due to malnutrition and deficiencies of fat-soluble vitamins), including neuromuscular abnormalities (typically in the first or second decade of life) secondary to vitamin E deficiency, poor bone mineralization and delayed bone maturation due to vitamin D deficiency, prolonged international normalized ratio (INR) due to vitamin K deficiency, mild ophthalmologic issues (e.g., micronystagmus, delayed dark adaptation, abnormal visual evoked potentials, and abnormal scotopic electroretinograms), and (in a small proportion of adults) cardiomyopathy with decreased ejection fraction. Affected individuals typically have marked hypocholesterolemia, low plasma apolipoprotein B levels, normal-to-low plasma triglyceride levels, and low serum concentrations of fat-soluble vitamins (A, D, E, and K). Endoscopy typically demonstrates a gelée blanche ("white hoar frosting") appearance of the duodenal mucosa.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/208651">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_336376"><div><strong>Oculogastrointestinal muscular dystrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>336376</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1848586</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">An extremely rare autosomal recessively inherited neuromuscular disease characterised by ocular manifestations such as ptosis and diplopia followed by chronic diarrhoea, malnutrition and intestinal pseudo-obstruction.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/336376">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_436369"><div><strong>Pancreatic insufficiency-anemia-hyperostosis syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>436369</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C2675184</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">This syndrome is characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis. It has been described in four children, three boys and one girl, from two consanguineous families. The disease is due to a mutation in the COX4I2 gene, encoding a mitochondrial cytochrome C oxidase sub-unit. Transmission is autosomal recessive.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/436369">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_411249"><div><strong>Isolated congenital hypoglossia/aglossia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>411249</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C2748587</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hypoglossia with situs inversus is a very rare congenital condition that likely represents a developmental field defect. Only sporadic cases have been reported (Faqeih et al., 2008). Hypoglossia is part of a group of malformation syndromes collectively termed 'oromandibular limb hypogenesis syndromes,' that usually include limb defects. Hall (1971) provided a classification system (see 103300). See also agnathia with holoprosencephaly (202650), which shows hypoglossia and situs inversus in addition to severe neurodevelopmental defects.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/411249">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_462264"><div><strong>Mitochondrial DNA depletion syndrome 4b</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>462264</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C3150914</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">POLG-related disorders comprise a continuum of overlapping phenotypes that were clinically defined before the molecular basis was known. POLG-related disorders can therefore be considered an overlapping spectrum of disease presenting from early childhood to late adulthood. The age of onset broadly correlates with the clinical phenotype. In individuals with early-onset disease (prior to age 12 years), liver involvement, feeding difficulties, seizures, hypotonia, and muscle weakness are the most common clinical features. This group has the worst prognosis. In the juvenile/adult-onset form (age 12-40 years), disease is typically characterized by peripheral neuropathy, ataxia, seizures, stroke-like episodes, and, in individuals with longer survival, progressive external ophthalmoplegia (PEO). This group generally has a better prognosis than the early-onset group. Late-onset disease (after age 40 years) is characterized by ptosis and PEO, with additional features such as peripheral neuropathy, ataxia, and muscle weakness. This group overall has the best prognosis.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/462264">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1631838"><div><strong>Mitochondrial DNA depletion syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1631838</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4551995</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Mitochondrial neurogastrointestinal encephalopathy (MNGIE) disease is characterized by progressive gastrointestinal dysmotility (manifesting as early satiety, nausea, dysphagia, gastroesophageal reflux, postprandial emesis, episodic abdominal pain and/or distention, and diarrhea); cachexia; ptosis/ophthalmoplegia or ophthalmoparesis; leukoencephalopathy; and demyelinating peripheral neuropathy (manifesting as paresthesias (tingling, numbness, and pain) and symmetric and distal weakness more prominently affecting the lower extremities). The order in which manifestations appear is unpredictable. Onset is usually between the first and fifth decades; in about 60% of individuals, symptoms begin before age 20 years.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1631838">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1785391"><div><strong>Visceral myopathy 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1785391</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C5542197</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">ACTG2 visceral myopathy is a disorder of smooth muscle dysfunction of the bladder and gastrointestinal system with phenotypic spectrum that ranges from mild to severe. Bladder involvement can range from neonatal megacystis and megaureter (with its most extreme form of prune belly syndrome) at the more severe end, to recurrent urinary tract infections and bladder dysfunction at the milder end. Intestinal involvement can range from malrotation, neonatal manifestations of microcolon, megacystis microcolon intestinal hypoperistalsis syndrome, and chronic intestinal pseudoobstruction (CIPO) in neonates at the more severe end to intermittent abdominal distention and functional intestinal obstruction at the milder end. Affected infants (with or without evidence of intestinal malrotation) often present with feeding intolerance and findings of non-mechanical bowel obstruction that persist after successful surgical correction of malrotation. Individuals who develop manifestations of CIPO in later childhood or adulthood often experience episodic waxing and waning of bowel motility. They may undergo frequent abdominal surgeries (perhaps related to malrotation or adhesions causing mechanical obstruction) resulting in resection of dilated segments of bowel, often becoming dependent on total parenteral nutrition (TPN).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1785391">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1823957"><div><strong>Neurodevelopmental disorder with epilepsy and brain atrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1823957</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C5774184</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Neurodevelopmental disorder with epilepsy and brain atrophy (NEDEBA) is an autosomal recessive disorder characterized by early-onset progressive myoclonus epilepsy with ataxia (summary by Bott et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1823957">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1823968"><div><strong>Liver disease, severe congenital</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1823968</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C5774195</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Severe congenital liver disease (SCOLIV) is an autosomal recessive disorder characterized by the onset of progressive hepatic dysfunction usually in the first years of life. Affected individuals show feeding difficulties with failure to thrive and features such as jaundice, hepatomegaly, and abdominal distension. Laboratory workup is consistent with hepatic insufficiency and may also show coagulation defects, anemia, or metabolic disturbances. Cirrhosis and hypernodularity are commonly observed on liver biopsy. Many patients die of liver failure in early childhood (Moreno Traspas et al., 2022).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1823968">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1824067"><div><strong>Congenital disorder of glycosylation, type IIy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1824067</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C5774294</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Congenital disorder of glycosylation type IIy (CDG2Y) is an autosomal recessive multisystemic congenital disorder characterized by poor overall growth and global developmental delay with impaired intellectual development. Other features may include hypotonia, seizures, brain imaging abnormalities, dysmorphic features, and various skeletal defects. Laboratory studies show a subtle type II glycosylation defect of serum transferrin (Tambe et al., 2020). For a general discussion of CDGs, see CDG1A (212065).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1824067">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_208651" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Chylomicron retention disease</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1824067" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Congenital disorder of glycosylation, type IIy</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_137954" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Congenital microvillous atrophy</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_42105" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hereditary fructosuria</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_411249" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Isolated congenital hypoglossia/aglossia</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (14)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1823968" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Liver disease, severe congenital</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_75704" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Lysinuric protein intolerance</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1631838" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mitochondrial DNA depletion syndrome 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_462264" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mitochondrial DNA depletion syndrome 4b</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1823957" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental disorder with epilepsy and brain atrophy</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_336376" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Oculogastrointestinal muscular dystrophy</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_436369" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pancreatic insufficiency-anemia-hyperostosis syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_36311" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Recessive dystrophic epidermolysis bullosa</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1785391" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Visceral myopathy 1</a></div></span></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/30181091">GLIM criteria for the diagnosis of malnutrition - A consensus report from the global clinical nutrition community.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cederholm T,
|
||
Jensen GL,
|
||
Correia MITD,
|
||
Gonzalez MC,
|
||
Fukushima R,
|
||
Higashiguchi T,
|
||
Baptista G,
|
||
Barazzoni R,
|
||
Blaauw R,
|
||
Coats A,
|
||
Crivelli A,
|
||
Evans DC,
|
||
Gramlich L,
|
||
Fuchs-Tarlovsky V,
|
||
Keller H,
|
||
Llido L,
|
||
Malone A,
|
||
Mogensen KM,
|
||
Morley JE,
|
||
Muscaritoli M,
|
||
Nyulasi I,
|
||
Pirlich M,
|
||
Pisprasert V,
|
||
de van der Schueren MAE,
|
||
Siltharm S,
|
||
Singer P,
|
||
Tappenden K,
|
||
Velasco N,
|
||
Waitzberg D,
|
||
Yamwong P,
|
||
Yu J,
|
||
Van Gossum A,
|
||
Compher C;
|
||
GLIM Core Leadership Committee;
|
||
GLIM Working Group</span><br />
|
||
<span class="medgenPMjournal">Clin Nutr</span>
|
||
2019 Feb;38(1):1-9.
|
||
Epub 2018 Sep 3
|
||
doi: 10.1016/j.clnu.2018.08.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30181091" target="_blank">30181091</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25799486">Diagnostic criteria for malnutrition - An ESPEN Consensus Statement.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cederholm T,
|
||
Bosaeus I,
|
||
Barazzoni R,
|
||
Bauer J,
|
||
Van Gossum A,
|
||
Klek S,
|
||
Muscaritoli M,
|
||
Nyulasi I,
|
||
Ockenga J,
|
||
Schneider SM,
|
||
de van der Schueren MA,
|
||
Singer P</span><br />
|
||
<span class="medgenPMjournal">Clin Nutr</span>
|
||
2015 Jun;34(3):335-40.
|
||
Epub 2015 Mar 9
|
||
doi: 10.1016/j.clnu.2015.03.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25799486" target="_blank">25799486</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22535923">Consensus statement: Academy of Nutrition and Dietetics and American Society for Parenteral and Enteral Nutrition: characteristics recommended for the identification and documentation of adult malnutrition (undernutrition).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">White JV,
|
||
Guenter P,
|
||
Jensen G,
|
||
Malone A,
|
||
Schofield M;
|
||
Academy Malnutrition Work Group;
|
||
A.S.P.E.N. Malnutrition Task Force;
|
||
A.S.P.E.N. Board of Directors</span><br />
|
||
<span class="medgenPMjournal">JPEN J Parenter Enteral Nutr</span>
|
||
2012 May;36(3):275-83.
|
||
doi: 10.1177/0148607112440285.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22535923" target="_blank">22535923</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22malnutrition%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (2338)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36716756">Malnutrition in older adults.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dent E,
|
||
Wright ORL,
|
||
Woo J,
|
||
Hoogendijk EO</span><br />
|
||
<span class="medgenPMjournal">Lancet</span>
|
||
2023 Mar 18;401(10380):951-966.
|
||
Epub 2023 Jan 27
|
||
doi: 10.1016/S0140-6736(22)02612-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36716756" target="_blank">36716756</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36243472">Nutrition and Wound Care.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Munoz N,
|
||
Litchford M,
|
||
Cereda E</span><br />
|
||
<span class="medgenPMjournal">Phys Med Rehabil Clin N Am</span>
|
||
2022 Nov;33(4):811-822.
|
||
Epub 2022 Sep 28
|
||
doi: 10.1016/j.pmr.2022.06.007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36243472" target="_blank">36243472</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35745121">Malnutrition Screening and Assessment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Serón-Arbeloa C,
|
||
Labarta-Monzón L,
|
||
Puzo-Foncillas J,
|
||
Mallor-Bonet T,
|
||
Lafita-López A,
|
||
Bueno-Vidales N,
|
||
Montoro-Huguet M</span><br />
|
||
<span class="medgenPMjournal">Nutrients</span>
|
||
2022 Jun 9;14(12)
|
||
doi: 10.3390/nu14122392.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35745121" target="_blank">35745121</a><a href="/pmc/articles/PMC9228435" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35215559">Malnutrition in Hospitalized Old Patients: Screening and Diagnosis, Clinical Outcomes, and Management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bellanti F,
|
||
Lo Buglio A,
|
||
Quiete S,
|
||
Vendemiale G</span><br />
|
||
<span class="medgenPMjournal">Nutrients</span>
|
||
2022 Feb 21;14(4)
|
||
doi: 10.3390/nu14040910.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35215559" target="_blank">35215559</a><a href="/pmc/articles/PMC8880030" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33733851">The role of nutrition in wound healing: an overview.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ghaly P,
|
||
Iliopoulos J,
|
||
Ahmad M</span><br />
|
||
<span class="medgenPMjournal">Br J Nurs</span>
|
||
2021 Mar 11;30(5):S38-S42.
|
||
doi: 10.12968/bjon.2021.30.5.S38.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33733851" target="_blank">33733851</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Malnutrition%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (26589)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36716756">Malnutrition in older adults.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dent E,
|
||
Wright ORL,
|
||
Woo J,
|
||
Hoogendijk EO</span><br />
|
||
<span class="medgenPMjournal">Lancet</span>
|
||
2023 Mar 18;401(10380):951-966.
|
||
Epub 2023 Jan 27
|
||
doi: 10.1016/S0140-6736(22)02612-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36716756" target="_blank">36716756</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35745121">Malnutrition Screening and Assessment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Serón-Arbeloa C,
|
||
Labarta-Monzón L,
|
||
Puzo-Foncillas J,
|
||
Mallor-Bonet T,
|
||
Lafita-López A,
|
||
Bueno-Vidales N,
|
||
Montoro-Huguet M</span><br />
|
||
<span class="medgenPMjournal">Nutrients</span>
|
||
2022 Jun 9;14(12)
|
||
doi: 10.3390/nu14122392.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35745121" target="_blank">35745121</a><a href="/pmc/articles/PMC9228435" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35215559">Malnutrition in Hospitalized Old Patients: Screening and Diagnosis, Clinical Outcomes, and Management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bellanti F,
|
||
Lo Buglio A,
|
||
Quiete S,
|
||
Vendemiale G</span><br />
|
||
<span class="medgenPMjournal">Nutrients</span>
|
||
2022 Feb 21;14(4)
|
||
doi: 10.3390/nu14040910.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35215559" target="_blank">35215559</a><a href="/pmc/articles/PMC8880030" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34936131">Key approaches to diagnosing malnutrition in adults.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Malone A,
|
||
Mogensen KM</span><br />
|
||
<span class="medgenPMjournal">Nutr Clin Pract</span>
|
||
2022 Feb;37(1):23-34.
|
||
Epub 2021 Dec 22
|
||
doi: 10.1002/ncp.10810.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34936131" target="_blank">34936131</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28933421">Severe childhood malnutrition.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bhutta ZA,
|
||
Berkley JA,
|
||
Bandsma RHJ,
|
||
Kerac M,
|
||
Trehan I,
|
||
Briend A</span><br />
|
||
<span class="medgenPMjournal">Nat Rev Dis Primers</span>
|
||
2017 Sep 21;3:17067.
|
||
doi: 10.1038/nrdp.2017.67.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28933421" target="_blank">28933421</a><a href="/pmc/articles/PMC7004825" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Malnutrition%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (13692)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35020271">Effectiveness of olanzapine in the treatment of anorexia nervosa: A systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Han R,
|
||
Bian Q,
|
||
Chen H</span><br />
|
||
<span class="medgenPMjournal">Brain Behav</span>
|
||
2022 Feb;12(2):e2498.
|
||
Epub 2022 Jan 12
|
||
doi: 10.1002/brb3.2498.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35020271" target="_blank">35020271</a><a href="/pmc/articles/PMC8865148" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30825493">Use of cyproheptadine to stimulate appetite and body weight gain: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Harrison ME,
|
||
Norris ML,
|
||
Robinson A,
|
||
Spettigue W,
|
||
Morrissey M,
|
||
Isserlin L</span><br />
|
||
<span class="medgenPMjournal">Appetite</span>
|
||
2019 Jun 1;137:62-72.
|
||
Epub 2019 Feb 27
|
||
doi: 10.1016/j.appet.2019.02.012.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30825493" target="_blank">30825493</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28264439">Protein Nutrition and Malnutrition in CKD and ESRD.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zha Y,
|
||
Qian Q</span><br />
|
||
<span class="medgenPMjournal">Nutrients</span>
|
||
2017 Feb 27;9(3)
|
||
doi: 10.3390/nu9030208.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28264439" target="_blank">28264439</a><a href="/pmc/articles/PMC5372871" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27637832">ESPEN guidelines on nutrition in cancer patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Arends J,
|
||
Bachmann P,
|
||
Baracos V,
|
||
Barthelemy N,
|
||
Bertz H,
|
||
Bozzetti F,
|
||
Fearon K,
|
||
Hütterer E,
|
||
Isenring E,
|
||
Kaasa S,
|
||
Krznaric Z,
|
||
Laird B,
|
||
Larsson M,
|
||
Laviano A,
|
||
Mühlebach S,
|
||
Muscaritoli M,
|
||
Oldervoll L,
|
||
Ravasco P,
|
||
Solheim T,
|
||
Strasser F,
|
||
de van der Schueren M,
|
||
Preiser JC</span><br />
|
||
<span class="medgenPMjournal">Clin Nutr</span>
|
||
2017 Feb;36(1):11-48.
|
||
Epub 2016 Aug 6
|
||
doi: 10.1016/j.clnu.2016.07.015.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27637832" target="_blank">27637832</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27436529">Oncology Evidence-Based Nutrition Practice Guideline for Adults.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Thompson KL,
|
||
Elliott L,
|
||
Fuchs-Tarlovsky V,
|
||
Levin RM,
|
||
Voss AC,
|
||
Piemonte T</span><br />
|
||
<span class="medgenPMjournal">J Acad Nutr Diet</span>
|
||
2017 Feb;117(2):297-310.e47.
|
||
Epub 2016 Jul 16
|
||
doi: 10.1016/j.jand.2016.05.010.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27436529" target="_blank">27436529</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Malnutrition%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (12816)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/28870921">Significance of Circulating Galectin-3 in Patients with Pancreatobiliary Cancer.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shimura T,
|
||
Shibata M,
|
||
Gonda K,
|
||
Kofunato Y,
|
||
Okada R,
|
||
Ishigame T,
|
||
Kimura T,
|
||
Kenjo A,
|
||
Kono K,
|
||
Marubashi S</span><br />
|
||
<span class="medgenPMjournal">Anticancer Res</span>
|
||
2017 Sep;37(9):4979-4986.
|
||
doi: 10.21873/anticanres.11909.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28870921" target="_blank">28870921</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26838530">Association Between Malnutrition and Clinical Outcomes in the Intensive Care Unit: A Systematic Review [Formula: see text].</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lew CCH,
|
||
Yandell R,
|
||
Fraser RJL,
|
||
Chua AP,
|
||
Chong MFF,
|
||
Miller M</span><br />
|
||
<span class="medgenPMjournal">JPEN J Parenter Enteral Nutr</span>
|
||
2017 Jul;41(5):744-758.
|
||
Epub 2016 Feb 2
|
||
doi: 10.1177/0148607115625638.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26838530" target="_blank">26838530</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12800351">Malnutrition in peritoneal dialysis patients: causes and diagnosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Garibotto G,
|
||
Saffioti S,
|
||
Russo R,
|
||
Verzola D,
|
||
Cappelli V,
|
||
Aloisi F,
|
||
Sofia A</span><br />
|
||
<span class="medgenPMjournal">Contrib Nephrol</span>
|
||
2003;(140):112-21.
|
||
doi: 10.1159/000071431.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12800351" target="_blank">12800351</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8059112">Cancer and poverty: breaking the cycle.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wilkes G,
|
||
Freeman H,
|
||
Prout M</span><br />
|
||
<span class="medgenPMjournal">Semin Oncol Nurs</span>
|
||
1994 May;10(2):79-88.
|
||
doi: 10.1016/s0749-2081(05)80061-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8059112" target="_blank">8059112</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14274169">MALNUTRITION AND INFECTION.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">SCRIMSHAW NS</span><br />
|
||
<span class="medgenPMjournal">Bordens Rev Nutr Res</span>
|
||
1965 Apr-Jun;26:17-29.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14274169" target="_blank">14274169</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Malnutrition%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (11830)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32359965">Clinical value of malnutrition.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Martín-Sánchez FJ,
|
||
Cuesta Triana F</span><br />
|
||
<span class="medgenPMjournal">Med Clin (Barc)</span>
|
||
2020 Sep 11;155(5):205-206.
|
||
Epub 2020 Apr 29
|
||
doi: 10.1016/j.medcli.2020.02.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32359965" target="_blank">32359965</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30720726">Are Predictive Energy Expenditure Equations Accurate in Cirrhosis?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Eslamparast T,
|
||
Vandermeer B,
|
||
Raman M,
|
||
Gramlich L,
|
||
Den Heyer V,
|
||
Belland D,
|
||
Ma M,
|
||
Tandon P</span><br />
|
||
<span class="medgenPMjournal">Nutrients</span>
|
||
2019 Feb 4;11(2)
|
||
doi: 10.3390/nu11020334.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30720726" target="_blank">30720726</a><a href="/pmc/articles/PMC6412603" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28771192">Evaluation of Blood Biomarkers Associated with Risk of Malnutrition in Older Adults: A Systematic Review and Meta-Analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhang Z,
|
||
Pereira SL,
|
||
Luo M,
|
||
Matheson EM</span><br />
|
||
<span class="medgenPMjournal">Nutrients</span>
|
||
2017 Aug 3;9(8)
|
||
doi: 10.3390/nu9080829.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28771192" target="_blank">28771192</a><a href="/pmc/articles/PMC5579622" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27999383">The Use of Enteral Nutrition in the Management of Stroke.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ojo O,
|
||
Brooke J</span><br />
|
||
<span class="medgenPMjournal">Nutrients</span>
|
||
2016 Dec 20;8(12)
|
||
doi: 10.3390/nu8120827.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27999383" target="_blank">27999383</a><a href="/pmc/articles/PMC5188480" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24259956">Diagnosis and treatment of pancreatic exocrine insufficiency.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lindkvist B</span><br />
|
||
<span class="medgenPMjournal">World J Gastroenterol</span>
|
||
2013 Nov 14;19(42):7258-66.
|
||
doi: 10.3748/wjg.v19.i42.7258.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24259956" target="_blank">24259956</a><a href="/pmc/articles/PMC3831207" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Malnutrition%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (15814)</a></div></div>
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<div class="nl"><a target="_blank" href="/pubmed/36324472">The risk of falls among the aging population: A systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Xu Q,
|
||
Ou X,
|
||
Li J</span><br />
|
||
<span class="medgenPMjournal">Front Public Health</span>
|
||
2022;10:902599.
|
||
Epub 2022 Oct 17
|
||
doi: 10.3389/fpubh.2022.902599.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36324472" target="_blank">36324472</a><a href="/pmc/articles/PMC9618649" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35377487">Prevalence of hospital-acquired malnutrition and modifiable determinants of nutritional deterioration during inpatient admissions: A systematic review of the evidence.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cass AR,
|
||
Charlton KE</span><br />
|
||
<span class="medgenPMjournal">J Hum Nutr Diet</span>
|
||
2022 Dec;35(6):1043-1058.
|
||
Epub 2022 Apr 26
|
||
doi: 10.1111/jhn.13009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35377487" target="_blank">35377487</a><a href="/pmc/articles/PMC9790482" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35066367">Determinants of malnutrition among children: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Katoch OR</span><br />
|
||
<span class="medgenPMjournal">Nutrition</span>
|
||
2022 Apr;96:111565.
|
||
Epub 2021 Dec 11
|
||
doi: 10.1016/j.nut.2021.111565.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35066367" target="_blank">35066367</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33253970">Managing malnutrition in COPD: A review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Keogh E,
|
||
Mark Williams E</span><br />
|
||
<span class="medgenPMjournal">Respir Med</span>
|
||
2021 Jan;176:106248.
|
||
Epub 2020 Nov 21
|
||
doi: 10.1016/j.rmed.2020.106248.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33253970" target="_blank">33253970</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31684843">Effect of nutrition on neurodegenerative diseases. A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bianchi VE,
|
||
Herrera PF,
|
||
Laura R</span><br />
|
||
<span class="medgenPMjournal">Nutr Neurosci</span>
|
||
2021 Oct;24(10):810-834.
|
||
Epub 2019 Nov 4
|
||
doi: 10.1080/1028415X.2019.1681088.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31684843" target="_blank">31684843</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Malnutrition%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (1280)</a></div></div>
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C0162429%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (1)</a></li>
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<li><a href="/gtr/tests?term=C0162429%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (1)</a></li>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22malnutrition%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Malnutrition%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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<a class="brieflinkpopperctrl" href="/gtr/tests?term=C0162429[DISCUI]" ref="log$=recordlinks">GTR</a>
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<a class="brieflinkpopperctrl" href="/gtr/tests?term=C0162429[DISCUI]&test_type=Clinical" ref="log$=recordlinks">GTR(Clinical)</a>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d49ff42f30673f7b1a7553">Malnutrition</a>
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<div class="ralinkpop offscreen_noflow">Malnutrition<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
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<div class="tertiary">MedGen</div>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=5" href="/portal/utils/pageresolver.fcgi?recordid=67d49fe484f3725e595b81fc">Table B. [OMIM Entries for Lysinuric Protein Intolerance (View All in OMIM)]. - ...</a>
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