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<meta name="keywords" content="C4025810, abnormal palmar dermatoglyphics, anatomical abnormality, 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="An abnormality of the dermatoglyphs, i.e., an abnormality of the patterns of ridges of the skin of palm of hand." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=871322
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ConceptID=C4025810
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Abnormal palmar dermatoglyphics</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>871322</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.">C4025810</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Anatomical Abnormality</dd></dl></div></div><table class="medgenTable"><tbody><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:0001018">HP:0001018</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">An abnormality of the dermatoglyphs, i.e., an abnormality of the patterns of ridges of the skin of palm of hand. [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_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">Abnormal palmar dermatoglyphics</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/536898" ref="tree=MeSH" title="MedGen record for Abnormality of limbs">Abnormality of limbs</a></span><ul><li><span class="TLline"><a href="/medgen/866555" ref="tree=MeSH" title="MedGen record for Abnormality of the upper limb">Abnormality of the upper limb</a></span><ul><li><span class="TLline"><a href="/medgen/6715" ref="tree=MeSH" title="MedGen record for Abnormality of the hand">Abnormality of the hand</a></span><ul><li><span class="TLline"><a href="/medgen/867564" ref="tree=MeSH" title="MedGen record for Abnormal palm morphology">Abnormal palm morphology</a></span><ul><li><span class="TLline"><a href="/medgen/892900" ref="tree=MeSH" title="MedGen record for Abnormal skin morphology of the palm">Abnormal skin morphology of the palm</a></span><ul><li><span class="matched_ds">Abnormal palmar dermatoglyphics</span><ul><li><span class="TLline"><a href="/medgen/870388" ref="tree=MeSH" title="MedGen record for Abnormal palmar dermal ridges">Abnormal palmar dermal ridges</a></span></li><li><span class="TLline"><a href="/medgen/526186" ref="tree=MeSH" title="MedGen record for Abnormality of the palmar creases">Abnormality of the palmar creases</a></span><ul><li><span class="TLline"><a href="/medgen/869379" ref="tree=MeSH" title="MedGen record for Aplasia/Hypoplasia of the palmar creases">Aplasia/Hypoplasia of the palmar creases</a></span><ul><li><span class="TLline"><a href="/medgen/866906" ref="tree=MeSH" title="MedGen record for Absent palmar crease">Absent palmar crease</a></span></li><li><span class="TLline"><a href="/medgen/346597" ref="tree=MeSH" title="MedGen record for Decreased palmar creases">Decreased palmar creases</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/866812" ref="tree=MeSH" title="MedGen record for Bridged palmar crease">Bridged palmar crease</a></span></li><li><span class="TLline"><a href="/medgen/387849" ref="tree=MeSH" title="MedGen record for Deep palmar crease">Deep palmar crease</a></span></li><li><span class="TLline"><a href="/medgen/1864396" ref="tree=MeSH" title="MedGen record for Hockey-stick palmar crease">Hockey-stick palmar crease</a></span></li><li><span class="TLline"><a href="/medgen/354610" ref="tree=MeSH" title="MedGen record for Multiple palmar creases">Multiple palmar creases</a></span></li><li><span class="TLline"><a href="/medgen/400690" ref="tree=MeSH" title="MedGen record for Prominent palmar flexion creases">Prominent palmar flexion creases</a></span></li><li><span class="TLline"><a href="/medgen/96108" ref="tree=MeSH" title="MedGen record for Single transverse palmar crease">Single transverse palmar crease</a></span><ul><li><span class="TLline"><a href="/medgen/354661" ref="tree=MeSH" title="MedGen record for Bilateral single transverse palmar creases">Bilateral single transverse palmar creases</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/869003" ref="tree=MeSH" title="MedGen record for Sydney crease">Sydney crease</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/870390" ref="tree=MeSH" title="MedGen record for Complex palmar dermatoglyphic pattern">Complex palmar dermatoglyphic pattern</a></span></li><li><span class="TLline"><a href="/medgen/870698" ref="tree=MeSH" title="MedGen record for Dermatoglyphic ridges abnormal">Dermatoglyphic ridges abnormal</a></span></li><li><span class="TLline"><a href="/medgen/870662" ref="tree=MeSH" title="MedGen record for Dermatoglyphic variants">Dermatoglyphic variants</a></span><ul><li><span class="TLline"><a href="/medgen/870400" ref="tree=MeSH" title="MedGen record for Index finger dermatoglyphic radial loop">Index finger dermatoglyphic radial loop</a></span></li><li><span class="TLline"><a href="/medgen/870401" ref="tree=MeSH" title="MedGen record for Unusual dermatoglyphics">Unusual dermatoglyphics</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/871318" ref="tree=MeSH" title="MedGen record for High axial triradius">High axial triradius</a></span></li><li><span class="TLline"><a href="/medgen/870666" ref="tree=MeSH" title="MedGen record for Increased dermatoglyphic whorls">Increased dermatoglyphic whorls</a></span></li><li><span class="TLline"><a href="/medgen/356420" ref="tree=MeSH" title="MedGen record for Prominent interdigital folds">Prominent interdigital folds</a></span></li></ul></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">
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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">
|
||
<div class="divPopper rprt" id="rdis_75567"><div><strong>CHARGE syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75567</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.">C0265354</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">CHD7 disorder encompasses the entire phenotypic spectrum of heterozygous CHD7 pathogenic variants that includes CHARGE syndrome as well as subsets of features that comprise the CHARGE syndrome phenotype. The mnemonic CHARGE syndrome, introduced in the premolecular era, stands for coloboma, heart defect, choanal atresia, retarded growth and development, genital hypoplasia, ear anomalies (including deafness). Following the identification of the genetic cause of CHD7 disorder, the phenotypic spectrum expanded to include cranial nerve anomalies, vestibular defects, cleft lip and/or palate, hypothyroidism, tracheoesophageal anomalies, brain anomalies, seizures, and renal anomalies. Life expectancy highly depends on the severity of manifestations; mortality can be high in the first few years when severe birth defects (particularly complex heart defects) are present and often complicated by airway and feeding issues. In childhood, adolescence, and adulthood, decreased life expectancy is likely related to a combination of residual heart defects, infections, aspiration or choking, respiratory issues including obstructive and central apnea, and possibly seizures. Despite these complications, the life expectancy for many individuals can be normal.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75567">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_162898"><div><strong>Microphthalmia, syndromic 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>162898</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.">C0796016</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Microphthalmia-ankyloblepharon-intellectual disability syndrome is characterized by microphthalmia, ankyloblepharon and intellectual deficit. It has been described in seven male patients from two generations of a Northern Ireland family. The causative gene is localized to the Xq27-q28 region. The syndrome is transmitted as an X-linked recessive trait.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/162898">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1823990"><div><strong>Dyskeratosis congenita, digenic</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1823990</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.">C5774217</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Digenic dyskeratosis congenita (DKCD) is characterized clinically by a combination of mucocutaneous features including abnormal skin pigmentation, nail dystrophy, thin hair, and oral leukoplakia. Some patients may have evidence of bone marrow failure, manifest as immune defects such as recurrent infections or hypogammaglobulinemia. Telomeres are shortened in patient cells. Individuals with DKCD may show severe adverse reactions to treatment with 5-FU (Tummala et al., 2022). For a discussion of genetic heterogeneity of dyskeratosis congenita, see DKCA1 (127550).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1823990">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_75567" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">CHARGE syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1823990" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Dyskeratosis congenita, digenic</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_162898" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Microphthalmia, syndromic 1</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/11807888">Application of robust pedigree analysis in studies of complex genotype-phenotype relationships in fragile X syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Loesch DZ,
|
||
Huggins RM,
|
||
Taylor AK</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet</span>
|
||
2002 Jan 15;107(2):136-42.
|
||
doi: 10.1002/ajmg.10129.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11807888" target="_blank">11807888</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/153214">Dermatoglyphics in parents of children with trisomy 21. Evaluation of their interest in genetic counselling.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ayme S,
|
||
Mattei MG,
|
||
Mattei JF,
|
||
Aurran Y,
|
||
Giraud F</span><br />
|
||
<span class="medgenPMjournal">Clin Genet</span>
|
||
1979 Jan;15(1):78-84.
|
||
doi: 10.1111/j.1399-0004.1979.tb02030.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/153214" target="_blank">153214</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormal%20palmar%20dermatoglyphics)%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 (2)</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/12795499">Further evidence that congenital dermatoglyphic abnormalities are associated with psychosis: a twin study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rosa A,
|
||
Fañanás L,
|
||
van Os J,
|
||
Ribchester T,
|
||
Davies N,
|
||
Arias B,
|
||
McDonald A,
|
||
Murray RM</span><br />
|
||
<span class="medgenPMjournal">Schizophr Bull</span>
|
||
2002;28(4):697-701.
|
||
doi: 10.1093/oxfordjournals.schbul.a006973.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12795499" target="_blank">12795499</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9349337">Dermatoglyphics in Darier's disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Blackwell D,
|
||
Shuster S</span><br />
|
||
<span class="medgenPMjournal">Br J Dermatol</span>
|
||
1997 Sep;137(3):401-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9349337" target="_blank">9349337</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3177443">A dermatoglyphic study of a group of Sicilian children with fragile-X syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Milone G,
|
||
Conti L,
|
||
Rizzo R,
|
||
Sanfilippo S,
|
||
Sammito V,
|
||
Romano C</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet</span>
|
||
1988 May-Jun;30(1-2):177-83.
|
||
doi: 10.1002/ajmg.1320300116.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3177443" target="_blank">3177443</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2969696">Dermatoglyphic patterns in senile dementia of Alzheimer's type.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Okra Podrabinek N,
|
||
Roudier M,
|
||
Lamour Y,
|
||
de Grouchy J</span><br />
|
||
<span class="medgenPMjournal">Ann Genet</span>
|
||
1988;31(2):91-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2969696" target="_blank">2969696</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/153214">Dermatoglyphics in parents of children with trisomy 21. Evaluation of their interest in genetic counselling.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ayme S,
|
||
Mattei MG,
|
||
Mattei JF,
|
||
Aurran Y,
|
||
Giraud F</span><br />
|
||
<span class="medgenPMjournal">Clin Genet</span>
|
||
1979 Jan;15(1):78-84.
|
||
doi: 10.1111/j.1399-0004.1979.tb02030.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/153214" target="_blank">153214</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20palmar%20dermatoglyphics%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 (36)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/4266116">Palmar dermatoglyphics of Down's syndrome: revisited.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Plato CC,
|
||
Cereghino JJ,
|
||
Steinberg FS</span><br />
|
||
<span class="medgenPMjournal">Pediatr Res</span>
|
||
1973 Mar;7(3):111-8.
|
||
doi: 10.1203/00006450-197303000-00002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4266116" target="_blank">4266116</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4119799">Unusual palm creases and unusual children. The Sydney line and "type C" palmar lines and their clinical significance in a child development clinic.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Johnson CF,
|
||
Opitz E</span><br />
|
||
<span class="medgenPMjournal">Clin Pediatr (Phila)</span>
|
||
1973 Feb;12(2):101-12.
|
||
doi: 10.1177/000992287301200214.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4119799" target="_blank">4119799</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/5486619">The genesis and significance of digital and palmar hand creases: preliminary report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Popich GA,
|
||
Smith DW</span><br />
|
||
<span class="medgenPMjournal">J Pediatr</span>
|
||
1970 Dec;77(6):1017-23.
|
||
doi: 10.1016/s0022-3476(70)80086-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/5486619" target="_blank">5486619</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/5661831">Dermatoglyphics and palmar creases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Davies PA</span><br />
|
||
<span class="medgenPMjournal">Nurs Times</span>
|
||
1968 Jul 26;64(30):994-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/5661831" target="_blank">5661831</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/5952910">Palmar dermatoglyphics in heart disease. Differential studies in Japanese and American populations with congenital and acquired heart diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Takashina T,
|
||
Yorifuji S</span><br />
|
||
<span class="medgenPMjournal">JAMA</span>
|
||
1966 Aug 29;197(9):689-92.
|
||
doi: 10.1001/jama.197.9.689.
|
||
<span class="bold">PMID: </span><a href="/pubmed/5952910" target="_blank">5952910</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20palmar%20dermatoglyphics%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 (43)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/23682364">Fingerprint changes and verification failure among patients with hand dermatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lee CK,
|
||
Chang CC,
|
||
Johar A,
|
||
Puwira O,
|
||
Roshidah B</span><br />
|
||
<span class="medgenPMjournal">JAMA Dermatol</span>
|
||
2013 Mar;149(3):295-9.
|
||
doi: 10.1001/jamadermatol.2013.1425.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23682364" target="_blank">23682364</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22610771">Incidence of simian crease in normal Nepalese children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Malla T,
|
||
Malla KK,
|
||
Gauchan E,
|
||
Brijesh S,
|
||
Sharma R</span><br />
|
||
<span class="medgenPMjournal">Kathmandu Univ Med J (KUMJ)</span>
|
||
2010 Oct-Dec;8(32):410-4.
|
||
doi: 10.3126/kumj.v8i4.6241.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22610771" target="_blank">22610771</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7719144">Congenital symmetrical weakness of the upper limbs resembling brachial plexus palsy: a possible sequel of drug toxicity in first trimester of pregnancy?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Philpot J,
|
||
Muntoni F,
|
||
Skellett S,
|
||
Dubowitz V</span><br />
|
||
<span class="medgenPMjournal">Neuromuscul Disord</span>
|
||
1995 Jan;5(1):67-9.
|
||
doi: 10.1016/0960-8966(94)e0028-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7719144" target="_blank">7719144</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/138837">Palmar crease variants and their clinical significance: a study of newborns at risk.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dar H,
|
||
Schmidt R,
|
||
Nitowsky HM</span><br />
|
||
<span class="medgenPMjournal">Pediatr Res</span>
|
||
1977 Feb;11(2):103-8.
|
||
doi: 10.1203/00006450-197702000-00004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/138837" target="_blank">138837</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4646554">The effect of absence of thumb on palmar dermatoglyphics.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Holt SB</span><br />
|
||
<span class="medgenPMjournal">J Med Genet</span>
|
||
1972 Dec;9(4):448-50.
|
||
doi: 10.1136/jmg.9.4.448.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4646554" target="_blank">4646554</a><a href="/pmc/articles/PMC1469068" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20palmar%20dermatoglyphics%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 (5)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/1786353">Palmar, plantar, and digital flexion creases: morphologic and clinical considerations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Schaumann BA,
|
||
Kimura S</span><br />
|
||
<span class="medgenPMjournal">Birth Defects Orig Artic Ser</span>
|
||
1991;27(2):229-52.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1786353" target="_blank">1786353</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3177443">A dermatoglyphic study of a group of Sicilian children with fragile-X syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Milone G,
|
||
Conti L,
|
||
Rizzo R,
|
||
Sanfilippo S,
|
||
Sammito V,
|
||
Romano C</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet</span>
|
||
1988 May-Jun;30(1-2):177-83.
|
||
doi: 10.1002/ajmg.1320300116.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3177443" target="_blank">3177443</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2969696">Dermatoglyphic patterns in senile dementia of Alzheimer's type.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Okra Podrabinek N,
|
||
Roudier M,
|
||
Lamour Y,
|
||
de Grouchy J</span><br />
|
||
<span class="medgenPMjournal">Ann Genet</span>
|
||
1988;31(2):91-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2969696" target="_blank">2969696</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/153214">Dermatoglyphics in parents of children with trisomy 21. Evaluation of their interest in genetic counselling.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ayme S,
|
||
Mattei MG,
|
||
Mattei JF,
|
||
Aurran Y,
|
||
Giraud F</span><br />
|
||
<span class="medgenPMjournal">Clin Genet</span>
|
||
1979 Jan;15(1):78-84.
|
||
doi: 10.1111/j.1399-0004.1979.tb02030.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/153214" target="_blank">153214</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14070922">THE SINGLE TRANSVERSE PALMAR CREASE IN INFANTS AND CHILDREN.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">DAVIES PA,
|
||
SMALLPEICE V</span><br />
|
||
<span class="medgenPMjournal">Dev Med Child Neurol</span>
|
||
1963 Oct;25:491-6.
|
||
doi: 10.1111/j.1469-8749.1963.tb10703.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14070922" target="_blank">14070922</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20palmar%20dermatoglyphics%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 (13)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33136290">Individuals lacking ridge detail: A case study in adermatoglyphia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cook HI,
|
||
Harrison K,
|
||
James H</span><br />
|
||
<span class="medgenPMjournal">J Forensic Sci</span>
|
||
2021 Jan;66(1):202-208.
|
||
Epub 2020 Nov 2
|
||
doi: 10.1111/1556-4029.14597.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33136290" target="_blank">33136290</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27650795">The status of dermatoglyphics as a biomarker of Tel Hashomer camptodactyly syndrome: a review of the literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wijerathne BT,
|
||
Meier RJ,
|
||
Agampodi SB</span><br />
|
||
<span class="medgenPMjournal">J Med Case Rep</span>
|
||
2016 Sep 20;10(1):258.
|
||
doi: 10.1186/s13256-016-1048-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27650795" target="_blank">27650795</a><a href="/pmc/articles/PMC5030737" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1786353">Palmar, plantar, and digital flexion creases: morphologic and clinical considerations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Schaumann BA,
|
||
Kimura S</span><br />
|
||
<span class="medgenPMjournal">Birth Defects Orig Artic Ser</span>
|
||
1991;27(2):229-52.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1786353" target="_blank">1786353</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3613239">Absence of palmar digital triradius d observed in 2,681 Japanese families and clinical significance.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Okajima M,
|
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Iwayanagi C</span><br />
|
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<span class="medgenPMjournal">Jinrui Idengaku Zasshi</span>
|
||
1986 Dec;31(4):331-6.
|
||
doi: 10.1007/BF01907932.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3613239" target="_blank">3613239</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/153214">Dermatoglyphics in parents of children with trisomy 21. Evaluation of their interest in genetic counselling.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ayme S,
|
||
Mattei MG,
|
||
Mattei JF,
|
||
Aurran Y,
|
||
Giraud F</span><br />
|
||
<span class="medgenPMjournal">Clin Genet</span>
|
||
1979 Jan;15(1):78-84.
|
||
doi: 10.1111/j.1399-0004.1979.tb02030.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/153214" target="_blank">153214</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20palmar%20dermatoglyphics%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 (34)</a></div></div>
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