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<meta name="keywords" content="C0085577, anaemia normocytic, anemia normocytic, disease or syndrome, normocytic anaemia, normocytic anemia, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="A kind of anemia in which the volume of the red blood cells is normal." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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||
UID=39310
|
||
ConceptID=C0085577
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Normocytic anemia</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>39310</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:">C0085577</span></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>anaemia normocytic; anemia normocytic; Normocytic anaemia; normocytic Anaemia; Normocytic Anemia; normocytic anemia; normocytic Anemia</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Normocytic anemia (300980002)</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:0001897">HP:0001897</a></td></tr>
|
||
<tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0004139" target="_blank">MONDO:0004139</a></td></tr>
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</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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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>
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||
<div class="portlet_content ln">A kind of anemia in which the volume of the red blood cells is normal. [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 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=C0085577[DISCUI]&test_type=Clinical" ref="ncbi_uid=39310">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 Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=39310" ref="ncbi_uid=39310">V</a></span></span><span class="TLline">Normocytic anemia</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/163092" ref="tree=MeSH" title="MedGen record for Abnormality of blood and blood-forming tissues">Abnormality of blood and blood-forming tissues</a></span><ul><li><span class="TLline"><a href="/medgen/488883" ref="tree=MeSH" title="MedGen record for Abnormal erythrocyte morphology">Abnormal erythrocyte morphology</a></span><ul><li><span class="TLline"><a href="/medgen/1526" ref="tree=MeSH" title="MedGen record for Anemia">Anemia</a></span><ul><li><span class="matched_ds">Normocytic anemia</span><ul><li><span class="TLline"><a href="/medgen/1916" ref="tree=MeSH" title="MedGen record for Hemolytic anemia">Hemolytic anemia</a></span><ul><li><span class="TLline"><a href="/medgen/1917" ref="tree=MeSH" title="MedGen record for Acquired hemolytic anemia">Acquired hemolytic anemia</a></span><ul><li><span class="TLline"><a href="/medgen/152905" ref="tree=MeSH" title="MedGen record for Hemolytic Anemia due to Disseminated Intravascular Coagulation">Hemolytic Anemia due to Disseminated Intravascular Coagulation</a></span></li><li><span class="TLline"><a href="/medgen/452755" ref="tree=MeSH" title="MedGen record for Immune Hemolytic Anemia">Immune Hemolytic Anemia</a></span></li><li><span class="TLline"><a href="/medgen/45122" ref="tree=MeSH" title="MedGen record for Non-autoimmune hemolytic anemia">Non-autoimmune hemolytic anemia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1918" ref="tree=MeSH" title="MedGen record for Autoimmune hemolytic anemia">Autoimmune hemolytic anemia</a></span><ul><li><span class="TLline"><a href="/medgen/450541" ref="tree=MeSH" title="MedGen record for Autoimmune hemolytic anemia, warm type">Autoimmune hemolytic anemia, warm type</a></span></li><li><span class="TLline"><a href="/medgen/580980" ref="tree=MeSH" title="MedGen record for Drug-induced autoimmune hemolytic anemia">Drug-induced autoimmune hemolytic anemia</a></span></li><li><span class="TLline"><a href="/medgen/75773" ref="tree=MeSH" title="MedGen record for Evans syndrome">Evans syndrome</a></span></li><li><span class="TLline"><a href="/medgen/930926" ref="tree=MeSH" title="MedGen record for Mixed-type autoimmune hemolytic anemia">Mixed-type autoimmune hemolytic anemia</a></span></li><li><span class="TLline"><a href="/medgen/863232" ref="tree=MeSH" title="MedGen record for STAT3-related early-onset multisystem autoimmune disease">STAT3-related early-onset multisystem autoimmune disease</a></span></li><li><span class="TLline"><a href="/medgen/1685970" ref="tree=MeSH" title="MedGen record for Warm Antibody Autoimmune Hemolytic Anemia">Warm Antibody Autoimmune Hemolytic Anemia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/237230" ref="tree=MeSH" title="MedGen record for Chronic hemolytic anemia">Chronic hemolytic anemia</a></span></li><li><span class="TLline"><a href="/medgen/1613268" ref="tree=MeSH" title="MedGen record for Cold-induced hemolysis">Cold-induced hemolysis</a></span></li><li><span class="TLline"><a href="/medgen/870825" ref="tree=MeSH" title="MedGen record for Compensated hemolytic anemia">Compensated hemolytic anemia</a></span></li><li><span class="TLline"><a href="/medgen/105458" ref="tree=MeSH" title="MedGen record for Coombs-positive hemolytic anemia">Coombs-positive hemolytic anemia</a></span></li><li><span class="TLline"><a href="/medgen/870829" ref="tree=MeSH" title="MedGen record for Drug-sensitive hemolytic anemia">Drug-sensitive hemolytic anemia</a></span></li><li><span class="TLline"><a href="/medgen/347161" ref="tree=MeSH" title="MedGen record for Episodic hemolytic anemia">Episodic hemolytic anemia</a></span></li><li><span class="TLline"><a href="/medgen/870728" ref="tree=MeSH" title="MedGen record for Exercise-induced hemolysis">Exercise-induced hemolysis</a></span></li><li><span class="TLline"><a href="/medgen/1919" ref="tree=MeSH" title="MedGen record for Familial hemolytic anemia">Familial hemolytic anemia</a></span><ul><li><span class="TLline"><a href="/medgen/543748" ref="tree=MeSH" title="MedGen record for Anemia due to membrane defect">Anemia due to membrane defect</a></span></li><li><span class="TLline"><a href="/medgen/8064" ref="tree=MeSH" title="MedGen record for Congenital dyserythropoietic anemia">Congenital dyserythropoietic anemia</a></span></li><li><span class="TLline"><a href="/medgen/284" ref="tree=MeSH" title="MedGen record for Congenital nonspherocytic hemolytic anemia">Congenital nonspherocytic hemolytic anemia</a></span></li><li><span class="TLline"><a href="/medgen/473706" ref="tree=MeSH" title="MedGen record for G6PD deficiency">G6PD deficiency</a></span></li><li><span class="TLline"><a href="/medgen/287" ref="tree=MeSH" title="MedGen record for Hb SS disease">Hb SS disease</a></span></li><li><span class="TLline"><a href="/medgen/6789" ref="tree=MeSH" title="MedGen record for Hemoglobin C disease">Hemoglobin C disease</a></span></li><li><span class="TLline"><a href="/medgen/41747" ref="tree=MeSH" title="MedGen record for Hereditary elliptocytosis">Hereditary elliptocytosis</a></span></li><li><span class="TLline"><a href="/medgen/52450" ref="tree=MeSH" title="MedGen record for Hereditary spherocytosis">Hereditary spherocytosis</a></span></li><li><span class="TLline"><a href="/medgen/21121" ref="tree=MeSH" title="MedGen record for Thalassemia">Thalassemia</a></span></li><li><span class="TLline"><a href="/medgen/349893" ref="tree=MeSH" title="MedGen record for Triosephosphate isomerase deficiency">Triosephosphate isomerase deficiency</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/867286" ref="tree=MeSH" title="MedGen record for Fava bean-induced hemolytic anemia">Fava bean-induced hemolytic anemia</a></span></li><li><span class="TLline"><a href="/medgen/4667" ref="tree=MeSH" title="MedGen record for Favism">Favism</a></span></li><li><span class="TLline"><a href="/medgen/148583" ref="tree=MeSH" title="MedGen record for Heinz body anemia">Heinz body anemia</a></span></li><li><span class="TLline"><a href="/medgen/42403" ref="tree=MeSH" title="MedGen record for Hemolytic-uremic syndrome">Hemolytic-uremic syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/444141" ref="tree=MeSH" title="MedGen record for Atypical hemolytic-uremic syndrome">Atypical hemolytic-uremic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1826167" ref="tree=MeSH" title="MedGen record for Atypical hemolytic-uremic syndrome with DGKE deficiency">Atypical hemolytic-uremic syndrome with DGKE deficiency</a></span></li><li><span class="TLline"><a href="/medgen/341256" ref="tree=MeSH" title="MedGen record for Cobalamin C disease">Cobalamin C disease</a></span></li><li><span class="TLline"><a href="/medgen/449003" ref="tree=MeSH" title="MedGen record for D-plus hemolytic uremic syndrome (D+HUS)">D-plus hemolytic uremic syndrome (D+HUS)</a></span></li><li><span class="TLline"><a href="/medgen/692756" ref="tree=MeSH" title="MedGen record for Diarrhea-associated hemolytic uremic syndrome">Diarrhea-associated hemolytic uremic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/692757" ref="tree=MeSH" title="MedGen record for Diarrhea-negative hemolytic uremic syndrome">Diarrhea-negative hemolytic uremic syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1826072" ref="tree=MeSH" title="MedGen record for Infection-related hemolytic uremic syndrome">Infection-related hemolytic uremic syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/812455" ref="tree=MeSH" title="MedGen record for Increased red cell hemolysis by shear stress">Increased red cell hemolysis by shear stress</a></span></li><li><span class="TLline"><a href="/medgen/870731" ref="tree=MeSH" title="MedGen record for Macrocytic hemolytic disease">Macrocytic hemolytic disease</a></span></li><li><span class="TLline"><a href="/medgen/65120" ref="tree=MeSH" title="MedGen record for Microangiopathic hemolytic anemia">Microangiopathic hemolytic anemia</a></span></li><li><span class="TLline"><a href="/medgen/871250" ref="tree=MeSH" title="MedGen record for Nonspherocytic hemolytic anemia">Nonspherocytic hemolytic anemia</a></span></li><li><span class="TLline"><a href="/medgen/9205" ref="tree=MeSH" title="MedGen record for Paroxysmal Hemoglobinuria">Paroxysmal Hemoglobinuria</a></span></li><li><span class="TLline"><a href="/medgen/870730" ref="tree=MeSH" title="MedGen record for Spontaneous hemolytic crises">Spontaneous hemolytic crises</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</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_82895"><div><strong>HNSHA due to aldolase A deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>82895</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.">C0272066</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Aldolase A deficiency is an autosomal recessive disorder associated with hereditary hemolytic anemia (Kishi et al., 1987).</div>
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||
<div class="spaceAbove nowrap">See: <a href="/medgen/82895">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_344640"><div><strong>Methylcobalamin deficiency type cblE</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>344640</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.">C1856057</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Disorders of intracellular cobalamin metabolism have a variable phenotype and age of onset that are influenced by the severity and location within the pathway of the defect. The prototype and best understood phenotype is cblC; it is also the most common of these disorders. The age of initial presentation of cblC spans a wide range: In utero with fetal presentation of nonimmune hydrops, cardiomyopathy, and intrauterine growth restriction. Newborns, who can have microcephaly, poor feeding, and encephalopathy. Infants, who can have poor feeding and slow growth, neurologic abnormality, and, rarely, hemolytic uremic syndrome (HUS). Toddlers, who can have poor growth, progressive microcephaly, cytopenias (including megaloblastic anemia), global developmental delay, encephalopathy, and neurologic signs such as hypotonia and seizures. Adolescents and adults, who can have neuropsychiatric symptoms, progressive cognitive decline, thromboembolic complications, and/or subacute combined degeneration of the spinal cord.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/344640">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_349893"><div><strong>Triosephosphate isomerase deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>349893</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.">C1860808</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Triosephosphate isomerase deficiency (TPID) is an autosomal recessive multisystem disorder characterized by congenital hemolytic anemia, and progressive neuromuscular dysfunction beginning in early childhood. Many patients die from respiratory failure in childhood. The neurologic syndrome is variable, but usually includes lower motor neuron dysfunction with hypotonia, muscle weakness and atrophy, and hyporeflexia. Some patients may show additional signs such as dystonic posturing and/or spasticity. Laboratory studies show intracellular accumulation of dihydroxyacetone phosphate (DHAP), particularly in red blood cells (summary by Fermo et al., 2010).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/349893">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_461693"><div><strong>Hemolytic anemia due to hexokinase deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>461693</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.">C3150343</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Nonspherocytic haemolytic anaemia due to hexokinase deficiency is characterised by severe hemolysis, appearing in infancy. Seventeen affected families have been reported so far. Transmission is autosomal recessive. Mutations have been described in <i>HK1</i>, the gene that encodes red blood cell-specific hexokinase-R.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/461693">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_863078"><div><strong>Diamond-Blackfan anemia 13</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>863078</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.">C4014641</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Diamond-Blackfan anemia (DBA) is characterized by a profound normochromic and usually macrocytic anemia with normal leukocytes and platelets, congenital malformations in up to 50%, and growth deficiency in 30% of affected individuals. The hematologic complications occur in 90% of affected individuals during the first year of life. The phenotypic spectrum ranges from a mild form (e.g., mild anemia or no anemia with only subtle erythroid abnormalities, physical malformations without anemia) to a severe form of fetal anemia resulting in nonimmune hydrops fetalis. DBA is associated with an increased risk for acute myelogenous leukemia (AML), myelodysplastic syndrome (MDS), and solid tumors including osteogenic sarcoma.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/863078">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_934786"><div><strong>Immunodeficiency 47</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934786</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.">C4310819</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Immunodeficiency-47 (IMD47) is an X-linked recessive complex syndrome characterized by liver dysfunction, recurrent bacterial infections, hypogammaglobulinemia, and defective glycosylation of serum proteins. Some patients also have neurologic abnormalities (summary by Jansen et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/934786">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1634617"><div><strong>Shwachman-Diamond syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1634617</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.">C4693704</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Shwachman-Diamond syndrome (SDS) is characterized by exocrine pancreatic dysfunction with malabsorption, malnutrition, and growth failure; hematologic abnormalities with single- or multilineage cytopenias and susceptibility to myelodysplastic syndrome (MDS) and acute myelogenous leukemia (AML); and bone abnormalities. In almost all affected children, persistent or intermittent neutropenia is an early finding. Short stature and recurrent infections are common.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1634617">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1731112"><div><strong>Arthrogryposis multiplex congenita 5</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1731112</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.">C5436453</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Arthrogryposis multiplex congenita-5 (AMC5) is an autosomal recessive disorder characterized by severe joint contractures apparent at birth. Affected individuals usually have hypertonia and abnormal movements suggestive of dystonia, as well as feeding and/or breathing difficulties. More variable features may include poor overall growth, strabismus, dysmorphic facies, and global developmental delay with impaired speech (summary by Kariminejad et al., 2017).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1731112">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1731112" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Arthrogryposis multiplex congenita 5</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_863078" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Diamond-Blackfan anemia 13</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_461693" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hemolytic anemia due to hexokinase deficiency</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_82895" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">HNSHA due to aldolase A deficiency</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934786" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Immunodeficiency 47</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_344640" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Methylcobalamin deficiency type cblE</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1634617" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Shwachman-Diamond syndrome 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_349893" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Triosephosphate isomerase deficiency</a></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/39700365">Anemia in Infants and Children: Evaluation and Treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Raleigh MF,
|
||
Yano AS,
|
||
Shaffer NE</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
2024 Dec;110(6):612-620.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39700365" target="_blank">39700365</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38489926">Compliance With NCCN Guidelines for Evaluation and Treatment of Anemia Among Patients With Solid Tumors.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hufnagel DH,
|
||
Bos LM,
|
||
Brown AJ,
|
||
Prescott LS</span><br />
|
||
<span class="medgenPMjournal">J Natl Compr Canc Netw</span>
|
||
2024 Mar 15;22(3)
|
||
doi: 10.6004/jnccn.2023.7108.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38489926" target="_blank">38489926</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8172230">Pathogenesis and treatment of the anemia of chronic disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Krantz SB</span><br />
|
||
<span class="medgenPMjournal">Am J Med Sci</span>
|
||
1994 May;307(5):353-9.
|
||
doi: 10.1097/00000441-199405000-00009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8172230" target="_blank">8172230</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22normocytic%20anemia%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 (7)</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/37390396">Anemia: Microcytic Anemia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rampon K</span><br />
|
||
<span class="medgenPMjournal">FP Essent</span>
|
||
2023 Jul;530:12-16.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37390396" target="_blank">37390396</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36153722">Scurvy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Krečak I,
|
||
Babić G,
|
||
Skelin M</span><br />
|
||
<span class="medgenPMjournal">Acta Dermatovenerol Croat</span>
|
||
2022 Jul;30(1):59-60.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36153722" target="_blank">36153722</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28400547">Anemia in thyroid diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Szczepanek-Parulska E,
|
||
Hernik A,
|
||
Ruchała M</span><br />
|
||
<span class="medgenPMjournal">Pol Arch Intern Med</span>
|
||
2017 May 31;127(5):352-360.
|
||
Epub 2017 Mar 28
|
||
doi: 10.20452/pamw.3985.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28400547" target="_blank">28400547</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26926814">Iron Deficiency and Other Types of Anemia in Infants and Children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang M</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
2016 Feb 15;93(4):270-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26926814" target="_blank">26926814</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20540485">Evaluation of anemia in children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Janus J,
|
||
Moerschel SK</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
2010 Jun 15;81(12):1462-71.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20540485" target="_blank">20540485</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Normocytic%20anemia%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 (81)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37327996">Pure red cell aplasia: The second hundred years.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Means RT Jr</span><br />
|
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<span class="medgenPMjournal">Am J Med Sci</span>
|
||
2023 Sep;366(3):160-166.
|
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Epub 2023 Jun 14
|
||
doi: 10.1016/j.amjms.2023.06.009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37327996" target="_blank">37327996</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35788790">Sickle Cell Disease: A Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kavanagh PL,
|
||
Fasipe TA,
|
||
Wun T</span><br />
|
||
<span class="medgenPMjournal">JAMA</span>
|
||
2022 Jul 5;328(1):57-68.
|
||
doi: 10.1001/jama.2022.10233.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35788790" target="_blank">35788790</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28400547">Anemia in thyroid diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Szczepanek-Parulska E,
|
||
Hernik A,
|
||
Ruchała M</span><br />
|
||
<span class="medgenPMjournal">Pol Arch Intern Med</span>
|
||
2017 May 31;127(5):352-360.
|
||
Epub 2017 Mar 28
|
||
doi: 10.20452/pamw.3985.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28400547" target="_blank">28400547</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26926814">Iron Deficiency and Other Types of Anemia in Infants and Children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang M</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
2016 Feb 15;93(4):270-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26926814" target="_blank">26926814</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20540485">Evaluation of anemia in children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Janus J,
|
||
Moerschel SK</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
2010 Jun 15;81(12):1462-71.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20540485" target="_blank">20540485</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Normocytic%20anemia%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 (153)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39603678">Bupropion-induced pancytopenia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kim JL,
|
||
Chercover D,
|
||
Masoudi H,
|
||
Foltz L</span><br />
|
||
<span class="medgenPMjournal">BMJ Case Rep</span>
|
||
2024 Nov 26;17(11)
|
||
doi: 10.1136/bcr-2024-262831.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39603678" target="_blank">39603678</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35788790">Sickle Cell Disease: A Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kavanagh PL,
|
||
Fasipe TA,
|
||
Wun T</span><br />
|
||
<span class="medgenPMjournal">JAMA</span>
|
||
2022 Jul 5;328(1):57-68.
|
||
doi: 10.1001/jama.2022.10233.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35788790" target="_blank">35788790</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20540485">Evaluation of anemia in children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Janus J,
|
||
Moerschel SK</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
2010 Jun 15;81(12):1462-71.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20540485" target="_blank">20540485</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10706651">Waldenström's macroglobulinemia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gertz MA,
|
||
Fonseca R,
|
||
Rajkumar SV</span><br />
|
||
<span class="medgenPMjournal">Oncologist</span>
|
||
2000;5(1):63-7.
|
||
doi: 10.1634/theoncologist.5-1-63.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10706651" target="_blank">10706651</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2884877">Glucagonoma syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bloom SR,
|
||
Polak JM</span><br />
|
||
<span class="medgenPMjournal">Am J Med</span>
|
||
1987 May 29;82(5B):25-36.
|
||
doi: 10.1016/0002-9343(87)90424-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2884877" target="_blank">2884877</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Normocytic%20anemia%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 (98)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/28400547">Anemia in thyroid diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Szczepanek-Parulska E,
|
||
Hernik A,
|
||
Ruchała M</span><br />
|
||
<span class="medgenPMjournal">Pol Arch Intern Med</span>
|
||
2017 May 31;127(5):352-360.
|
||
Epub 2017 Mar 28
|
||
doi: 10.20452/pamw.3985.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28400547" target="_blank">28400547</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26361692">Gromerulocystic Kidney Disease in a Transplanted Kidney: Case Report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kwiatkowska E,
|
||
Domanski L,
|
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Pawlik A</span><br />
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<span class="medgenPMjournal">Transplant Proc</span>
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2015 Sep;47(7):2251-3.
|
||
doi: 10.1016/j.transproceed.2015.06.004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26361692" target="_blank">26361692</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22860921">Waldenström macroglobulinemia: my way.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gertz M</span><br />
|
||
<span class="medgenPMjournal">Leuk Lymphoma</span>
|
||
2013 Mar;54(3):464-71.
|
||
Epub 2012 Aug 25
|
||
doi: 10.3109/10428194.2012.717173.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22860921" target="_blank">22860921</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22507796">Waldenström macroglobulinemia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gertz MA</span><br />
|
||
<span class="medgenPMjournal">Hematology</span>
|
||
2012 Apr;17 Suppl 1:S112-6.
|
||
doi: 10.1179/102453312X13336169156212.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22507796" target="_blank">22507796</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10706651">Waldenström's macroglobulinemia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gertz MA,
|
||
Fonseca R,
|
||
Rajkumar SV</span><br />
|
||
<span class="medgenPMjournal">Oncologist</span>
|
||
2000;5(1):63-7.
|
||
doi: 10.1634/theoncologist.5-1-63.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10706651" target="_blank">10706651</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Normocytic%20anemia%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 (59)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35788790">Sickle Cell Disease: A Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kavanagh PL,
|
||
Fasipe TA,
|
||
Wun T</span><br />
|
||
<span class="medgenPMjournal">JAMA</span>
|
||
2022 Jul 5;328(1):57-68.
|
||
doi: 10.1001/jama.2022.10233.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35788790" target="_blank">35788790</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30084153">Erythropoiesis and chronic kidney disease-related anemia: From physiology to new therapeutic advancements.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cernaro V,
|
||
Coppolino G,
|
||
Visconti L,
|
||
Rivoli L,
|
||
Lacquaniti A,
|
||
Santoro D,
|
||
Buemi A,
|
||
Loddo S,
|
||
Buemi M</span><br />
|
||
<span class="medgenPMjournal">Med Res Rev</span>
|
||
2019 Mar;39(2):427-460.
|
||
Epub 2018 Aug 6
|
||
doi: 10.1002/med.21527.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30084153" target="_blank">30084153</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25633233">Anemia in elderly hospitalized patients: prevalence and clinical impact.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Migone De Amicis M,
|
||
Poggiali E,
|
||
Motta I,
|
||
Minonzio F,
|
||
Fabio G,
|
||
Hu C,
|
||
Cappellini MD</span><br />
|
||
<span class="medgenPMjournal">Intern Emerg Med</span>
|
||
2015 Aug;10(5):581-6.
|
||
Epub 2015 Jan 30
|
||
doi: 10.1007/s11739-015-1197-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25633233" target="_blank">25633233</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22860921">Waldenström macroglobulinemia: my way.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gertz M</span><br />
|
||
<span class="medgenPMjournal">Leuk Lymphoma</span>
|
||
2013 Mar;54(3):464-71.
|
||
Epub 2012 Aug 25
|
||
doi: 10.3109/10428194.2012.717173.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22860921" target="_blank">22860921</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22507796">Waldenström macroglobulinemia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gertz MA</span><br />
|
||
<span class="medgenPMjournal">Hematology</span>
|
||
2012 Apr;17 Suppl 1:S112-6.
|
||
doi: 10.1179/102453312X13336169156212.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22507796" target="_blank">22507796</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Normocytic%20anemia%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 (53)</a></div></div>
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|
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