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<!--
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UID=488828
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ConceptID=C0266781
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Abnormality of the amniotic fluid</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>488828</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.">C0266781</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Abnormal amniotic fluid; Amniotic fluid abnormal</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Amniotic fluid abnormal (42170009); Abnormal amniotic fluid (42170009)</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:0001560">HP:0001560</a></td></tr>
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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">Abnormality of the amniotic fluid, which is the fluid contained in the amniotic sac surrounding the developing fetus. [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 unavailable round" title="Clinical test">C</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">Abnormality of the amniotic fluid</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/871309" ref="tree=MeSH" title="MedGen record for Abnormality of prenatal development or birth">Abnormality of prenatal development or birth</a></span><ul><li><span class="matched_ds">Abnormality of the amniotic fluid</span><ul><li><span class="TLline"><a href="/medgen/1841694" ref="tree=MeSH" title="MedGen record for Abnormal amniotic fluid protein concentration">Abnormal amniotic fluid protein concentration</a></span><ul><li><span class="TLline"><a href="/medgen/1841863" ref="tree=MeSH" title="MedGen record for Decreased amniotic fluid alpha-fetoprotein concentration">Decreased amniotic fluid alpha-fetoprotein concentration</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/676568" ref="tree=MeSH" title="MedGen record for Anhydramnios">Anhydramnios</a></span></li><li><span class="TLline"><a href="/medgen/355948" ref="tree=MeSH" title="MedGen record for Fetal polyuria">Fetal polyuria</a></span></li><li><span class="TLline"><a href="/medgen/604683" ref="tree=MeSH" title="MedGen record for Meconium stained amniotic fluid">Meconium stained amniotic fluid</a></span></li><li><span class="TLline"><a href="/medgen/86974" ref="tree=MeSH" title="MedGen record for Oligohydramnios">Oligohydramnios</a></span></li><li><span class="TLline"><a href="/medgen/6936" ref="tree=MeSH" title="MedGen record for Polyhydramnios">Polyhydramnios</a></span></li><li><span class="TLline"><a href="/medgen/1864074" ref="tree=MeSH" title="MedGen record for Snowflake effect in amniotic cavity">Snowflake effect in amniotic cavity</a></span></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">
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<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>
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<div class="portlet_content ln clinfeat">
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||
<div class="divPopper rprt" id="rdis_138111"><div><strong>PMM2-congenital disorder of glycosylation</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>138111</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:">C0349653</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">PMM2-CDG, the most common of a group of disorders of abnormal glycosylation of N-linked oligosaccharides, is divided into three clinical stages: infantile multisystem, late-infantile and childhood ataxia–intellectual disability, and adult stable disability. The clinical manifestations and course are highly variable, ranging from infants who die in the first year of life to mildly affected adults. Clinical findings tend to be similar in sibs. In the infantile multisystem presentation, infants show axial hypotonia, hyporeflexia, esotropia, and developmental delay. Feeding issues, vomiting, faltering growth, and developmental delay are frequently seen. Subcutaneous fat may be excessive over the buttocks and suprapubic region. Two distinct clinical courses are observed: (1) a nonfatal neurologic course with faltering growth, strabismus, developmental delay, cerebellar hypoplasia, and hepatopathy in infancy followed by neuropathy and retinitis pigmentosa in the first or second decade; and (2) a more severe neurologic-multivisceral course with approximately 20% mortality in the first year of life. The late-infantile and childhood ataxia–intellectual disability stage, which begins between ages three and ten years, is characterized by hypotonia, ataxia, severely delayed language and motor development, inability to walk, and IQ of 40 to 70; other findings include seizures, stroke-like episodes or transient unilateral loss of function, coagulopathy, retinitis pigmentosa, joint contractures, and skeletal deformities. In the adult stable disability stage, intellectual ability is stable; peripheral neuropathy is variable, progressive retinitis pigmentosa and myopia are seen, thoracic and spinal deformities with osteoporosis worsen, and premature aging is observed; females may lack secondary sexual development and males may exhibit decreased testicular volume. Hypogonadotropic hypogonadism and coagulopathy may occur. The risk for deep venous thrombosis is increased.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/138111">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_344338"><div><strong>Lethal congenital contracture syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>344338</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.">C1854664</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive lethal congenital contracture syndrome (LCCS) is the most severe, neonatally lethal, form of arthrogryposis (see 108120), a disorder characterized by congenital nonprogressive joint contractures. The contractures can involve the upper or lower limbs and/or the vertebral column, leading to various degrees of flexion or extension limitations evident at birth (summary by Markus et al., 2012). Genetic Heterogeneity of Lethal Congenital Contracture Syndrome See also lethal congenital contracture syndrome-2 (LCCS2; 607598), caused by mutation in the ERBB3 gene (190151); LCCS3 (611369), caused by mutation in the PIP5K1C gene (606102); LCCS4 (614915), caused by mutation in the MYBPC1 gene (160794); LCCS5 (615368), caused by mutation in the DNM2 gene (602378); LCCS6 (616248), caused by mutation in the ZBTB42 gene (613915); LCCS7 (616286), caused by mutation in the CNTNAP1 gene (602346); LCCS8 (616287), caused by mutation in the ADCY6 gene (600294); LCCS9 (616503), caused by mutation in the ADGRG6 gene (612243); LCCS10 (617022), caused by mutation in the NEK9 gene (609798); and LCCS11 (617194), caused by mutation in the GLDN gene (608603).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/344338">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_370665"><div><strong>Mitochondrial trifunctional protein deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>370665</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.">C1969443</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Long-chain hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency and trifunctional protein (TFP) deficiency are caused by impairment of mitochondrial TFP. TFP has three enzymatic activities – long-chain enoyl-CoA hydratase, long-chain 3-hydroxyacyl-CoA dehydrogenase, and long-chain 3-ketoacyl-CoA thiolase. In individuals with LCHAD deficiency, there is isolated deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase, while deficiency of all three enzymes occurs in individuals with TFP deficiency. Individuals with TFP deficiency can present with a severe-to-mild phenotype, while individuals with LCHAD deficiency typically present with a severe-to-intermediate phenotype. Neonates with the severe phenotype present within a few days of birth with hypoglycemia, hepatomegaly, encephalopathy, and often cardiomyopathy. The intermediate phenotype is characterized by hypoketotic hypoglycemia precipitated by infection or fasting in infancy. The mild (late-onset) phenotype is characterized by myopathy and/or neuropathy. Long-term complications include peripheral neuropathy and retinopathy.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/370665">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_419308"><div><strong>ALG1-congenital disorder of glycosylation</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>419308</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.">C2931005</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Congenital disorders of glycosylation (CDGs) comprise a group of multisystem diseases with mostly severe psychomotor and mental retardation. Type I CDG comprises those disorders in which there are defects that affect biosynthesis of dolichol-linked oligosaccharides in the cytosol or the endoplasmic reticulum (ER), as well as defects involving the transfer of oligosaccharides onto nascent glycoproteins. Type II CDG comprises all defects of further trimming and elongation of N-linked oligosaccharides in the ER and Golgi (Schwarz et al., 2004). CDG1K is a type I CDG characterized by predominant neurologic involvement. Survival ranges from the second day of life to adulthood. The liver is affected in a minority of patients and shows hepatomegaly, edema, ascites, cholestatic jaundice, portal hypertension, and Budd-Chiari syndrome (summary by Marques-da-Silva et al., 2017). For a general discussion of CDGs, see CDG1A (212065).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/419308">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_419308" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">ALG1-congenital disorder of glycosylation</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_344338" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Lethal congenital contracture syndrome 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_370665" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mitochondrial trifunctional protein deficiency</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_138111" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">PMM2-congenital disorder of glycosylation</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/38233317">Clinical chorioamnionitis at term: definition, pathogenesis, microbiology, diagnosis, and treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jung E,
|
||
Romero R,
|
||
Suksai M,
|
||
Gotsch F,
|
||
Chaemsaithong P,
|
||
Erez O,
|
||
Conde-Agudelo A,
|
||
Gomez-Lopez N,
|
||
Berry SM,
|
||
Meyyazhagan A,
|
||
Yoon BH</span><br />
|
||
<span class="medgenPMjournal">Am J Obstet Gynecol</span>
|
||
2024 Mar;230(3S):S807-S840.
|
||
Epub 2023 Mar 21
|
||
doi: 10.1016/j.ajog.2023.02.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38233317" target="_blank">38233317</a><a href="/pmc/articles/PMC11288098" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28869276">Amniocentesis and chorionic villus sampling for prenatal diagnosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Alfirevic Z,
|
||
Navaratnam K,
|
||
Mujezinovic F</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2017 Sep 4;9(9):CD003252.
|
||
doi: 10.1002/14651858.CD003252.pub2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28869276" target="_blank">28869276</a><a href="/pmc/articles/PMC6483702" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4142084">Prenatal diagnosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ferguson-Smith MA</span><br />
|
||
<span class="medgenPMjournal">Practitioner</span>
|
||
1974 Nov;213(1277):655-66.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4142084" target="_blank">4142084</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormality%20of%20the%20amniotic%20fluid)%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 (700)</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/6204708">Prenatal diagnosis. Amniocentesis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McNay MB,
|
||
Whitfield CR</span><br />
|
||
<span class="medgenPMjournal">Br J Hosp Med</span>
|
||
1984 Jun;31(6):406-7, 410-11, 13 passim.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6204708" target="_blank">6204708</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/391467">Diagnosis of structural abnormalities in the fetus.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">De Vore GR,
|
||
Hobbins JC</span><br />
|
||
<span class="medgenPMjournal">Clin Perinatol</span>
|
||
1979 Sep;6(2):293-319.
|
||
<span class="bold">PMID: </span><a href="/pubmed/391467" target="_blank">391467</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/74855">Prenatal diagnosis of genetic disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Miller WA,
|
||
Erbe RW</span><br />
|
||
<span class="medgenPMjournal">South Med J</span>
|
||
1978 Feb;71(2):201-6.
|
||
doi: 10.1097/00007611-197802000-00031.
|
||
<span class="bold">PMID: </span><a href="/pubmed/74855" target="_blank">74855</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4915801">The physiology and clinical importance of amniotic fluid. A review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ostergard DR</span><br />
|
||
<span class="medgenPMjournal">Obstet Gynecol Surv</span>
|
||
1970 Apr;25(4):297-319.
|
||
doi: 10.1097/00006254-197004000-00001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4915801" target="_blank">4915801</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14133668">NEONATOLOGY.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">MCKAY RJ Jr</span><br />
|
||
<span class="medgenPMjournal">N Engl J Med</span>
|
||
1964 Jun 11;270:1292-9 CONCL.
|
||
doi: 10.1056/NEJM196406112702406.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14133668" target="_blank">14133668</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20amniotic%20fluid%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 (2016)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/6357346">Amniotic fluid cell types and culture.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gosden CM</span><br />
|
||
<span class="medgenPMjournal">Br Med Bull</span>
|
||
1983 Oct;39(4):348-54.
|
||
doi: 10.1093/oxfordjournals.bmb.a071847.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6357346" target="_blank">6357346</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/391467">Diagnosis of structural abnormalities in the fetus.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">De Vore GR,
|
||
Hobbins JC</span><br />
|
||
<span class="medgenPMjournal">Clin Perinatol</span>
|
||
1979 Sep;6(2):293-319.
|
||
<span class="bold">PMID: </span><a href="/pubmed/391467" target="_blank">391467</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/74855">Prenatal diagnosis of genetic disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Miller WA,
|
||
Erbe RW</span><br />
|
||
<span class="medgenPMjournal">South Med J</span>
|
||
1978 Feb;71(2):201-6.
|
||
doi: 10.1097/00007611-197802000-00031.
|
||
<span class="bold">PMID: </span><a href="/pubmed/74855" target="_blank">74855</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4127367">Letter: Amniotic-fluid macrophages and anencephaly.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sutherland GR,
|
||
Brock DJ,
|
||
Scrimgeour JB</span><br />
|
||
<span class="medgenPMjournal">Lancet</span>
|
||
1973 Nov 10;2(7837):1098-9.
|
||
doi: 10.1016/s0140-6736(73)92720-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4127367" target="_blank">4127367</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4591074">Antenatal diagnosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Maidman JE</span><br />
|
||
<span class="medgenPMjournal">Obstet Gynecol Annu</span>
|
||
1972;1:65-101.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4591074" target="_blank">4591074</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20amniotic%20fluid%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 (3093)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38233317">Clinical chorioamnionitis at term: definition, pathogenesis, microbiology, diagnosis, and treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jung E,
|
||
Romero R,
|
||
Suksai M,
|
||
Gotsch F,
|
||
Chaemsaithong P,
|
||
Erez O,
|
||
Conde-Agudelo A,
|
||
Gomez-Lopez N,
|
||
Berry SM,
|
||
Meyyazhagan A,
|
||
Yoon BH</span><br />
|
||
<span class="medgenPMjournal">Am J Obstet Gynecol</span>
|
||
2024 Mar;230(3S):S807-S840.
|
||
Epub 2023 Mar 21
|
||
doi: 10.1016/j.ajog.2023.02.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38233317" target="_blank">38233317</a><a href="/pmc/articles/PMC11288098" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36131564">Haemostatic support in postpartum haemorrhage: A review of the literature and expert opinion.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hofer S,
|
||
Blaha J,
|
||
Collins PW,
|
||
Ducloy-Bouthors AS,
|
||
Guasch E,
|
||
Labate F,
|
||
Lança F,
|
||
Nyfløt LT,
|
||
Steiner K,
|
||
Van de Velde M</span><br />
|
||
<span class="medgenPMjournal">Eur J Anaesthesiol</span>
|
||
2023 Jan 1;40(1):29-38.
|
||
Epub 2022 Sep 22
|
||
doi: 10.1097/EJA.0000000000001744.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36131564" target="_blank">36131564</a><a href="/pmc/articles/PMC9794135" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35817950">The Pathophysiology of Labor Dystocia: Theme with Variations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kissler K,
|
||
Hurt KJ</span><br />
|
||
<span class="medgenPMjournal">Reprod Sci</span>
|
||
2023 Mar;30(3):729-742.
|
||
Epub 2022 Jul 11
|
||
doi: 10.1007/s43032-022-01018-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35817950" target="_blank">35817950</a><a href="/pmc/articles/PMC10388369" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30659586">Prenatal detection of esophageal atresia: A systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pardy C,
|
||
D'Antonio F,
|
||
Khalil A,
|
||
Giuliani S</span><br />
|
||
<span class="medgenPMjournal">Acta Obstet Gynecol Scand</span>
|
||
2019 Jun;98(6):689-699.
|
||
Epub 2019 Mar 6
|
||
doi: 10.1111/aogs.13536.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30659586" target="_blank">30659586</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28710882">Mid-trimester preterm premature rupture of membranes (PPROM): etiology, diagnosis, classification, international recommendations of treatment options and outcome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tchirikov M,
|
||
Schlabritz-Loutsevitch N,
|
||
Maher J,
|
||
Buchmann J,
|
||
Naberezhnev Y,
|
||
Winarno AS,
|
||
Seliger G</span><br />
|
||
<span class="medgenPMjournal">J Perinat Med</span>
|
||
2018 Jul 26;46(5):465-488.
|
||
doi: 10.1515/jpm-2017-0027.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28710882" target="_blank">28710882</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20amniotic%20fluid%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 (462)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/18065301">Dysplastic kidneys.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Winyard P,
|
||
Chitty LS</span><br />
|
||
<span class="medgenPMjournal">Semin Fetal Neonatal Med</span>
|
||
2008 Jun;13(3):142-51.
|
||
Epub 2007 Dec 11
|
||
doi: 10.1016/j.siny.2007.10.009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18065301" target="_blank">18065301</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9199843">Oligohydramnios: sonographic diagnosis and clinical implications.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hill LM</span><br />
|
||
<span class="medgenPMjournal">Clin Obstet Gynecol</span>
|
||
1997 Jun;40(2):314-27.
|
||
doi: 10.1097/00003081-199706000-00008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9199843" target="_blank">9199843</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3311512">Diagnostic ultrasonography.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McNay MB</span><br />
|
||
<span class="medgenPMjournal">Baillieres Clin Obstet Gynaecol</span>
|
||
1987 Mar;1(1):29-53.
|
||
doi: 10.1016/s0950-3552(87)80022-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3311512" target="_blank">3311512</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6204708">Prenatal diagnosis. Amniocentesis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McNay MB,
|
||
Whitfield CR</span><br />
|
||
<span class="medgenPMjournal">Br J Hosp Med</span>
|
||
1984 Jun;31(6):406-7, 410-11, 13 passim.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6204708" target="_blank">6204708</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6024471">Influence of maternal renal infection on the foetus and infant.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Patrick MJ</span><br />
|
||
<span class="medgenPMjournal">Arch Dis Child</span>
|
||
1967 Apr;42(222):208-13.
|
||
doi: 10.1136/adc.42.222.208.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6024471" target="_blank">6024471</a><a href="/pmc/articles/PMC2019709" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20amniotic%20fluid%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 (1062)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33885190">Semiquantitative Assessment of Amniotic Fluid Among Individuals With and Without Diabetes Mellitus.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bicocca MJ,
|
||
Qureshey EJ,
|
||
Chauhan SP,
|
||
Hernandez-Andrade E,
|
||
Sibai BM,
|
||
Nowlen C,
|
||
Stafford I</span><br />
|
||
<span class="medgenPMjournal">J Ultrasound Med</span>
|
||
2022 Feb;41(2):447-455.
|
||
Epub 2021 Apr 22
|
||
doi: 10.1002/jum.15725.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33885190" target="_blank">33885190</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33774758">The Potential Role of miRNAs as Predictive Biomarkers in Neurodevelopmental Disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Juvale IIA,
|
||
Che Has AT</span><br />
|
||
<span class="medgenPMjournal">J Mol Neurosci</span>
|
||
2021 Jul;71(7):1338-1355.
|
||
Epub 2021 Mar 27
|
||
doi: 10.1007/s12031-021-01825-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33774758" target="_blank">33774758</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22039031">Amniotic fluid and the clinical relevance of the sonographically estimated amniotic fluid volume: oligohydramnios.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Magann EF,
|
||
Sandlin AT,
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||
Ounpraseuth ST</span><br />
|
||
<span class="medgenPMjournal">J Ultrasound Med</span>
|
||
2011 Nov;30(11):1573-85.
|
||
doi: 10.7863/jum.2011.30.11.1573.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22039031" target="_blank">22039031</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3311512">Diagnostic ultrasonography.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McNay MB</span><br />
|
||
<span class="medgenPMjournal">Baillieres Clin Obstet Gynaecol</span>
|
||
1987 Mar;1(1):29-53.
|
||
doi: 10.1016/s0950-3552(87)80022-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3311512" target="_blank">3311512</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/954299">Perinatal observations on the etiology of congenital dislocation of the hip.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dunn PM</span><br />
|
||
<span class="medgenPMjournal">Clin Orthop Relat Res</span>
|
||
1976 Sep;(119):11-22.
|
||
<span class="bold">PMID: </span><a href="/pubmed/954299" target="_blank">954299</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20amniotic%20fluid%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 (1231)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/37164492">Intrapartum amnioinfusion reduces meconium aspiration syndrome and improves neonatal outcomes in patients with meconium-stained fluid: a systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Davis JD,
|
||
Sanchez-Ramos L,
|
||
McKinney JA,
|
||
Lin L,
|
||
Kaunitz AM</span><br />
|
||
<span class="medgenPMjournal">Am J Obstet Gynecol</span>
|
||
2023 May;228(5S):S1179-S1191.e19.
|
||
Epub 2023 Mar 18
|
||
doi: 10.1016/j.ajog.2022.07.047.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37164492" target="_blank">37164492</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33797605">A systematic review of pregnant women with COVID-19 and their neonates.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mirbeyk M,
|
||
Saghazadeh A,
|
||
Rezaei N</span><br />
|
||
<span class="medgenPMjournal">Arch Gynecol Obstet</span>
|
||
2021 Jul;304(1):5-38.
|
||
Epub 2021 Apr 2
|
||
doi: 10.1007/s00404-021-06049-z.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33797605" target="_blank">33797605</a><a href="/pmc/articles/PMC8017514" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30659586">Prenatal detection of esophageal atresia: A systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pardy C,
|
||
D'Antonio F,
|
||
Khalil A,
|
||
Giuliani S</span><br />
|
||
<span class="medgenPMjournal">Acta Obstet Gynecol Scand</span>
|
||
2019 Jun;98(6):689-699.
|
||
Epub 2019 Mar 6
|
||
doi: 10.1111/aogs.13536.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30659586" target="_blank">30659586</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28869276">Amniocentesis and chorionic villus sampling for prenatal diagnosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Alfirevic Z,
|
||
Navaratnam K,
|
||
Mujezinovic F</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2017 Sep 4;9(9):CD003252.
|
||
doi: 10.1002/14651858.CD003252.pub2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28869276" target="_blank">28869276</a><a href="/pmc/articles/PMC6483702" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27425793">Non-vector-borne transmission of Zika virus: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Grischott F,
|
||
Puhan M,
|
||
Hatz C,
|
||
Schlagenhauf P</span><br />
|
||
<span class="medgenPMjournal">Travel Med Infect Dis</span>
|
||
2016 Jul-Aug;14(4):313-30.
|
||
Epub 2016 Jul 15
|
||
doi: 10.1016/j.tmaid.2016.07.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27425793" target="_blank">27425793</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20amniotic%20fluid%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 (28)</a></div></div>
|
||
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|
||
</div></div></div></div></div></div></div>
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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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=(abnormality%20of%20the%20amniotic%20fluid)%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(%22Abnormality%20of%20the%20amniotic%20fluid%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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