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<meta name="keywords" content="C1856912, disproportionately short middle phalanges, finding, shortening of all middle phalanges of the fingers, 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="Short, hypoplastic middle phalanx of finger, affecting all fingers." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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||
UID=347331
|
||
ConceptID=C1856912
|
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Shortening of all middle phalanges of the fingers</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>347331</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.">C1856912</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Disproportionately short middle phalanges</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
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<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0006110">HP:0006110</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">Short, hypoplastic middle phalanx of finger, affecting all fingers. [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 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">Shortening of all middle phalanges of the fingers</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/763618" ref="tree=MeSH" title="MedGen record for Abnormal digit morphology">Abnormal digit morphology</a></span><ul><li><span class="TLline"><a href="/medgen/436247" ref="tree=MeSH" title="MedGen record for Abnormal finger morphology">Abnormal finger morphology</a></span><ul><li><span class="TLline"><a href="/medgen/867254" ref="tree=MeSH" title="MedGen record for Abnormal finger phalanx morphology">Abnormal finger phalanx morphology</a></span><ul><li><span class="TLline"><a href="/medgen/869762" ref="tree=MeSH" title="MedGen record for Abnormal middle phalanx morphology of the hand">Abnormal middle phalanx morphology of the hand</a></span><ul><li><span class="TLline"><a href="/medgen/354674" ref="tree=MeSH" title="MedGen record for Aplasia/Hypoplasia of the middle phalanges of the hand">Aplasia/Hypoplasia of the middle phalanges of the hand</a></span><ul><li><span class="TLline"><a href="/medgen/337690" ref="tree=MeSH" title="MedGen record for Short middle phalanx of finger">Short middle phalanx of finger</a></span><ul><li><span class="matched_ds">Shortening of all middle phalanges of the fingers</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<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_67390"><div><strong>Pfeiffer syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>67390</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.">C0220658</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Pfeiffer syndrome is an autosomal dominant craniosynostosis syndrome with characteristic anomalies of the hands and feet. Three clinical subtypes, which have important diagnostic and prognostic implications, have been identified. Type 1, the classic syndrome, is compatible with life and consists of craniosynostosis, midface deficiency, broad thumbs, broad great toes, brachydactyly, and variable syndactyly. Type 2 consists of cloverleaf skull with Pfeiffer hands and feet, together with ankylosis of the elbows. Type 3 is similar to type 2 but without cloverleaf skull. Ocular proptosis is severe, and the anterior cranial base is markedly short. Various visceral malformations have been found in association with type 3. Early demise is characteristic of types 2 and 3 (Cohen, 1993). Cohen and Barone (1994) further tabulated the findings in the 3 types of Pfeiffer syndrome.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/67390">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_78557"><div><strong>Borjeson-Forssman-Lehmann syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>78557</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.">C0265339</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Borjeson-Forssman-Lehmann syndrome (BFLS) is an uncommon X-linked intellectual developmental disorder that evolves with age. Clinical manifestations in males are quite variable, with the most consistent features being initial hypotonia, mild to moderate impaired intellectual development, large fleshy ears, underdeveloped genitalia, gynecomastia, truncal obesity, tapering fingers, and shortening of the fourth and fifth toes. Heterozygous females may have a milder similar clinical phenotype, which can include hypothyroidism; however, many carrier females appear unaffected (summary by Crawford et al., 2006).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/78557">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_140926"><div><strong>Wolcott-Rallison dysplasia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>140926</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.">C0432217</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Wolcott-Rallison syndrome is a rare autosomal recessive disorder characterized by permanent neonatal or early infancy insulin-dependent diabetes. Epiphyseal dysplasia, osteoporosis, and growth retardation develop at a later age. Other frequent multisystem manifestations include hepatic and renal dysfunction, mental retardation, and cardiovascular abnormalities (summary by Delepine et al., 2000).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/140926">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_163223"><div><strong>Spondyloperipheral dysplasia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>163223</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.">C0796173</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Spondyloperipheral dysplasia is a disorder that impairs bone growth. The signs and symptoms of this condition can vary among affected individuals. People with spondyloperipheral dysplasia typically have short stature, with a short torso, short arms and legs, and short fingers and toes (brachydactyly). These parts of the body are not proportional to one another (disproportionate short stature) in people with this condition. Affected individuals also tend to have flattened bones of the spine (platyspondyly) and inward- and upward-turning feet (clubfoot). Some people with spondyloperipheral dysplasia may also experience nearsightedness (myopia) or hearing loss. </div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/163223">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_371600"><div><strong>Craniosynostosis, Adelaide type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>371600</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.">C1833578</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/371600">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_331103"><div><strong>Hand-foot-genital syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>331103</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:">C1841679</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hand-foot-genital syndrome (HFGS) is characterized by limb malformations and urogenital defects. Mild-to-severe bilateral shortening of the thumbs and great toes, caused primarily by shortening of the distal phalanx and/or the first metacarpal or metatarsal, is the most common limb malformation and results in impaired dexterity or apposition of the thumbs. Urogenital malformations include abnormalities of the ureters and urethra and various degrees of incomplete müllerian fusion in females, and hypospadias of variable severity with or without chordee in males. Vesicoureteral reflux, recurrent urinary tract infections, and chronic pyelonephritis may occur; fertility is normal.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/331103">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_419681"><div><strong>Acromesomelic dysplasia 2C, Hunter-Thompson type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>419681</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.">C2930970</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Acromesomelic dysplasia-2C (AMD2C) is characterized by skeletal abnormalities restricted to the limbs; the craniofacial skeleton and axial skeletal structures are normal. The severity of the long bone shortening progresses in a proximal to distal direction. The hands and feet are most severely affected, but the distal phalanges are relative normal. Affected individuals have joint dislocations but the number of joints involved is not constant (summary by Thomas et al., 1996). For a discussion of genetic heterogeneity of acromesomelic dysplasia, see AMD1 (602875).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/419681">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_419681" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Acromesomelic dysplasia 2C, Hunter-Thompson type</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_78557" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Borjeson-Forssman-Lehmann syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_371600" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Craniosynostosis, Adelaide type</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_331103" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hand-foot-genital syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_67390" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pfeiffer syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_163223" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spondyloperipheral dysplasia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_140926" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Wolcott-Rallison dysplasia</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/27117125">Functional and radiographic evaluation of the treatment of traumatic bone loss of the hand using the Masquelet technique.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Moris V,
|
||
Loisel F,
|
||
Cheval D,
|
||
See LA,
|
||
Tchurukdichian A,
|
||
Pluvy I,
|
||
Gindraux F,
|
||
Pauchot J,
|
||
Zwetyenga N,
|
||
Obert L</span><br />
|
||
<span class="medgenPMjournal">Hand Surg Rehabil</span>
|
||
2016 Apr;35(2):114-21.
|
||
Epub 2016 Mar 16
|
||
doi: 10.1016/j.hansur.2015.11.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27117125" target="_blank">27117125</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25792522">Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Maas SM,
|
||
Shaw AC,
|
||
Bikker H,
|
||
Lüdecke HJ,
|
||
van der Tuin K,
|
||
Badura-Stronka M,
|
||
Belligni E,
|
||
Biamino E,
|
||
Bonati MT,
|
||
Carvalho DR,
|
||
Cobben J,
|
||
de Man SA,
|
||
Den Hollander NS,
|
||
Di Donato N,
|
||
Garavelli L,
|
||
Grønborg S,
|
||
Herkert JC,
|
||
Hoogeboom AJ,
|
||
Jamsheer A,
|
||
Latos-Bielenska A,
|
||
Maat-Kievit A,
|
||
Magnani C,
|
||
Marcelis C,
|
||
Mathijssen IB,
|
||
Nielsen M,
|
||
Otten E,
|
||
Ousager LB,
|
||
Pilch J,
|
||
Plomp A,
|
||
Poke G,
|
||
Poluha A,
|
||
Posmyk R,
|
||
Rieubland C,
|
||
Silengo M,
|
||
Simon M,
|
||
Steichen E,
|
||
Stumpel C,
|
||
Szakszon K,
|
||
Polonkai E,
|
||
van den Ende J,
|
||
van der Steen A,
|
||
van Essen T,
|
||
van Haeringen A,
|
||
van Hagen JM,
|
||
Verheij JB,
|
||
Mannens MM,
|
||
Hennekam RC</span><br />
|
||
<span class="medgenPMjournal">Eur J Med Genet</span>
|
||
2015 May;58(5):279-92.
|
||
Epub 2015 Mar 16
|
||
doi: 10.1016/j.ejmg.2015.03.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25792522" target="_blank">25792522</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24164128">Conservative treatment of fractures of the proximal phalanx: an option even for unstable fracture patterns.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Held M,
|
||
Jordaan P,
|
||
Laubscher M,
|
||
Singer M,
|
||
Solomons M</span><br />
|
||
<span class="medgenPMjournal">Hand Surg</span>
|
||
2013;18(2):229-34.
|
||
doi: 10.1142/S0218810413500287.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24164128" target="_blank">24164128</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(shortening%20of%20all%20middle%20phalanges%20of%20the%20fingers)%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 (3)</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/35307585">Long-term follow-up of one-stage artificial dermis reconstruction surgery for fingertip defects with exposed phalanx.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang J,
|
||
Huang Z,
|
||
Cueva Jumbo JC,
|
||
Sha K</span><br />
|
||
<span class="medgenPMjournal">Hand Surg Rehabil</span>
|
||
2022 Jun;41(3):353-361.
|
||
Epub 2022 Mar 17
|
||
doi: 10.1016/j.hansur.2022.02.012.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35307585" target="_blank">35307585</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33642092">Natural History and Characteristics of Hand Exostoses in Multiple Hereditary Exostoses.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Komura S,
|
||
Matsumoto K,
|
||
Hirakawa A,
|
||
Akiyama H</span><br />
|
||
<span class="medgenPMjournal">J Hand Surg Am</span>
|
||
2021 Sep;46(9):815.e1-815.e12.
|
||
Epub 2021 Feb 26
|
||
doi: 10.1016/j.jhsa.2020.12.011.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33642092" target="_blank">33642092</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30665870">Middle phalangectomy with shortening fusion of the fifth finger in Dupuytren's digital hooks.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Raimbeau G,
|
||
Bigorre N,
|
||
Balti W,
|
||
Rabarin F,
|
||
Jeudy J,
|
||
Fouque PA,
|
||
Cesari B,
|
||
Saint-Cast Y</span><br />
|
||
<span class="medgenPMjournal">Hand Surg Rehabil</span>
|
||
2019 Apr;38(2):108-113.
|
||
Epub 2019 Jan 19
|
||
doi: 10.1016/j.hansur.2018.12.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30665870" target="_blank">30665870</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24164128">Conservative treatment of fractures of the proximal phalanx: an option even for unstable fracture patterns.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Held M,
|
||
Jordaan P,
|
||
Laubscher M,
|
||
Singer M,
|
||
Solomons M</span><br />
|
||
<span class="medgenPMjournal">Hand Surg</span>
|
||
2013;18(2):229-34.
|
||
doi: 10.1142/S0218810413500287.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24164128" target="_blank">24164128</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22695440">Distraction lengthening by callotasis of traumatically shortened bones of the hand.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hosny GA,
|
||
Kandel WA</span><br />
|
||
<span class="medgenPMjournal">J Trauma Acute Care Surg</span>
|
||
2012 Jun;72(6):1676-80.
|
||
doi: 10.1097/TA.0b013e31824b177a.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22695440" target="_blank">22695440</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Shortening%20of%20all%20middle%20phalanges%20of%20the%20fingers%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 (9)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33642092">Natural History and Characteristics of Hand Exostoses in Multiple Hereditary Exostoses.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Komura S,
|
||
Matsumoto K,
|
||
Hirakawa A,
|
||
Akiyama H</span><br />
|
||
<span class="medgenPMjournal">J Hand Surg Am</span>
|
||
2021 Sep;46(9):815.e1-815.e12.
|
||
Epub 2021 Feb 26
|
||
doi: 10.1016/j.jhsa.2020.12.011.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33642092" target="_blank">33642092</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30665870">Middle phalangectomy with shortening fusion of the fifth finger in Dupuytren's digital hooks.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Raimbeau G,
|
||
Bigorre N,
|
||
Balti W,
|
||
Rabarin F,
|
||
Jeudy J,
|
||
Fouque PA,
|
||
Cesari B,
|
||
Saint-Cast Y</span><br />
|
||
<span class="medgenPMjournal">Hand Surg Rehabil</span>
|
||
2019 Apr;38(2):108-113.
|
||
Epub 2019 Jan 19
|
||
doi: 10.1016/j.hansur.2018.12.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30665870" target="_blank">30665870</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29797497">Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB-related skeletal disorders in three fetuses and a 106-year-old exhibit.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rehder H,
|
||
Laccone F,
|
||
Kircher SG,
|
||
Schild RL,
|
||
Rapp C,
|
||
Bald R,
|
||
Schulze B,
|
||
Behunova J,
|
||
Neesen J,
|
||
Schoner K</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet A</span>
|
||
2018 Jul;176(7):1559-1568.
|
||
Epub 2018 May 23
|
||
doi: 10.1002/ajmg.a.38828.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29797497" target="_blank">29797497</a><a href="/pmc/articles/PMC6585644" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26945816">Brief Report: Peripheral Osteolysis in Adults Linked to ASAH1 (Acid Ceramidase) Mutations: A New Presentation of Farber's Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bonafé L,
|
||
Kariminejad A,
|
||
Li J,
|
||
Royer-Bertrand B,
|
||
Garcia V,
|
||
Mahdavi S,
|
||
Bozorgmehr B,
|
||
Lachman RL,
|
||
Mittaz-Crettol L,
|
||
Campos-Xavier B,
|
||
Nampoothiri S,
|
||
Unger S,
|
||
Rivolta C,
|
||
Levade T,
|
||
Superti-Furga A</span><br />
|
||
<span class="medgenPMjournal">Arthritis Rheumatol</span>
|
||
2016 Sep;68(9):2323-7.
|
||
Epub 2016 Jul 29
|
||
doi: 10.1002/art.39659.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26945816" target="_blank">26945816</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3981502">Thiemann's disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gewanter H,
|
||
Baum J</span><br />
|
||
<span class="medgenPMjournal">J Rheumatol</span>
|
||
1985 Feb;12(1):150-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3981502" target="_blank">3981502</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Shortening%20of%20all%20middle%20phalanges%20of%20the%20fingers%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 (12)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/27117125">Functional and radiographic evaluation of the treatment of traumatic bone loss of the hand using the Masquelet technique.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Moris V,
|
||
Loisel F,
|
||
Cheval D,
|
||
See LA,
|
||
Tchurukdichian A,
|
||
Pluvy I,
|
||
Gindraux F,
|
||
Pauchot J,
|
||
Zwetyenga N,
|
||
Obert L</span><br />
|
||
<span class="medgenPMjournal">Hand Surg Rehabil</span>
|
||
2016 Apr;35(2):114-21.
|
||
Epub 2016 Mar 16
|
||
doi: 10.1016/j.hansur.2015.11.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27117125" target="_blank">27117125</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6572713">Hydrocephalus and abnormal digits after failed first-trimester prostaglandin abortion attempt.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Collins FS,
|
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Mahoney MJ</span><br />
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<span class="medgenPMjournal">J Pediatr</span>
|
||
1983 Apr;102(4):620-1.
|
||
doi: 10.1016/s0022-3476(83)80204-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6572713" target="_blank">6572713</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Shortening%20of%20all%20middle%20phalanges%20of%20the%20fingers%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 (2)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35307585">Long-term follow-up of one-stage artificial dermis reconstruction surgery for fingertip defects with exposed phalanx.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang J,
|
||
Huang Z,
|
||
Cueva Jumbo JC,
|
||
Sha K</span><br />
|
||
<span class="medgenPMjournal">Hand Surg Rehabil</span>
|
||
2022 Jun;41(3):353-361.
|
||
Epub 2022 Mar 17
|
||
doi: 10.1016/j.hansur.2022.02.012.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35307585" target="_blank">35307585</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33642092">Natural History and Characteristics of Hand Exostoses in Multiple Hereditary Exostoses.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Komura S,
|
||
Matsumoto K,
|
||
Hirakawa A,
|
||
Akiyama H</span><br />
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<span class="medgenPMjournal">J Hand Surg Am</span>
|
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2021 Sep;46(9):815.e1-815.e12.
|
||
Epub 2021 Feb 26
|
||
doi: 10.1016/j.jhsa.2020.12.011.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33642092" target="_blank">33642092</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30665870">Middle phalangectomy with shortening fusion of the fifth finger in Dupuytren's digital hooks.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Raimbeau G,
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||
Bigorre N,
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||
Balti W,
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||
Rabarin F,
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Jeudy J,
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Fouque PA,
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Cesari B,
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Saint-Cast Y</span><br />
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<span class="medgenPMjournal">Hand Surg Rehabil</span>
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2019 Apr;38(2):108-113.
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Epub 2019 Jan 19
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|
||
<span class="bold">PMID: </span><a href="/pubmed/30665870" target="_blank">30665870</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24164128">Conservative treatment of fractures of the proximal phalanx: an option even for unstable fracture patterns.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Held M,
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Jordaan P,
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||
Laubscher M,
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<span class="medgenPMjournal">Hand Surg</span>
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2013;18(2):229-34.
|
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|
||
<span class="bold">PMID: </span><a href="/pubmed/24164128" target="_blank">24164128</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22695440">Distraction lengthening by callotasis of traumatically shortened bones of the hand.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hosny GA,
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Kandel WA</span><br />
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||
<span class="medgenPMjournal">J Trauma Acute Care Surg</span>
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||
2012 Jun;72(6):1676-80.
|
||
doi: 10.1097/TA.0b013e31824b177a.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22695440" target="_blank">22695440</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Shortening%20of%20all%20middle%20phalanges%20of%20the%20fingers%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 (9)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37881823">Distraction Osteogenesis for the Brachytelephalangic Thumb - A Case Report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yamazumi S,
|
||
Matsuura S,
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||
Miyawaki T</span><br />
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||
<span class="medgenPMjournal">J Hand Surg Asian Pac Vol</span>
|
||
2023 Oct;28(5):605-608.
|
||
Epub 2023 Oct 25
|
||
doi: 10.1142/S2424835523720189.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37881823" target="_blank">37881823</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33642092">Natural History and Characteristics of Hand Exostoses in Multiple Hereditary Exostoses.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Komura S,
|
||
Matsumoto K,
|
||
Hirakawa A,
|
||
Akiyama H</span><br />
|
||
<span class="medgenPMjournal">J Hand Surg Am</span>
|
||
2021 Sep;46(9):815.e1-815.e12.
|
||
Epub 2021 Feb 26
|
||
doi: 10.1016/j.jhsa.2020.12.011.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33642092" target="_blank">33642092</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27781989">Proximodistal interphalangeal arthrodesis of the little finger: A series of 7 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Honecker S,
|
||
Hidalgo Diaz JJ,
|
||
Naito K,
|
||
Pire E,
|
||
Prunières G,
|
||
Facca S,
|
||
Liverneaux P</span><br />
|
||
<span class="medgenPMjournal">Hand Surg Rehabil</span>
|
||
2016 Sep;35(4):262-265.
|
||
Epub 2016 Jul 27
|
||
doi: 10.1016/j.hansur.2016.06.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27781989" target="_blank">27781989</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27117125">Functional and radiographic evaluation of the treatment of traumatic bone loss of the hand using the Masquelet technique.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Moris V,
|
||
Loisel F,
|
||
Cheval D,
|
||
See LA,
|
||
Tchurukdichian A,
|
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Pluvy I,
|
||
Gindraux F,
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||
Pauchot J,
|
||
Zwetyenga N,
|
||
Obert L</span><br />
|
||
<span class="medgenPMjournal">Hand Surg Rehabil</span>
|
||
2016 Apr;35(2):114-21.
|
||
Epub 2016 Mar 16
|
||
doi: 10.1016/j.hansur.2015.11.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27117125" target="_blank">27117125</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19951580">Management of intra-articular fracture of the fingers via mini external fixator combined with limited internal fixation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Li WJ,
|
||
Tian W,
|
||
Tian GL,
|
||
Chen SL,
|
||
Zhang CQ,
|
||
Xue YH,
|
||
Li ZZ,
|
||
Zhu Y</span><br />
|
||
<span class="medgenPMjournal">Chin Med J (Engl)</span>
|
||
2009 Nov 5;122(21):2616-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19951580" target="_blank">19951580</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Shortening%20of%20all%20middle%20phalanges%20of%20the%20fingers%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 (16)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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|
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|
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|
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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=(shortening%20of%20all%20middle%20phalanges%20of%20the%20fingers)%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></ul></div>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d4315b84f3725e5925ee27">Shortening of all middle phalanges of the fingers</a>
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<div class="ralinkpop offscreen_noflow">Shortening of all middle phalanges of the fingers<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
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