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<!--
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UID=341658
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ConceptID=C1856954
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Plantar hyperkeratosis</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>341658</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.">C1856954</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Plantar hyperkeratoses</td></tr>
|
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<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:0007556">HP:0007556</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">Hyperkeratosis affecting the sole of the foot. [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">Plantar hyperkeratosis</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/871273" ref="tree=MeSH" title="MedGen record for Abnormality of the integument">Abnormality of the integument</a></span><ul><li><span class="TLline"><a href="/medgen/1845238" ref="tree=MeSH" title="MedGen record for Abnormality of the skin">Abnormality of the skin</a></span><ul><li><span class="TLline"><a href="/medgen/869110" ref="tree=MeSH" title="MedGen record for Abnormal skin morphology">Abnormal skin morphology</a></span><ul><li><span class="TLline"><a href="/medgen/868988" ref="tree=MeSH" title="MedGen record for Regional abnormality of skin">Regional abnormality of skin</a></span><ul><li><span class="TLline"><a href="/medgen/866600" ref="tree=MeSH" title="MedGen record for Abnormality of the plantar skin of foot">Abnormality of the plantar skin of foot</a></span><ul><li><span class="matched_ds">Plantar hyperkeratosis</span><ul><li><span class="TLline"><a href="/medgen/1052677" ref="tree=MeSH" title="MedGen record for Hiker feet">Hiker feet</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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</div>
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|
||
<div class="portlet mgSection" id="ID_112">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_12147"><div><strong>Werner syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>12147</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:">C0043119</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Werner syndrome is characterized by the premature appearance of features associated with normal aging and cancer predisposition. Individuals with Werner syndrome develop normally until the end of the first decade. The first sign is the lack of a growth spurt during the early teen years. Early findings (usually observed in the 20s) include loss and graying of hair, hoarseness, and scleroderma-like skin changes, followed by bilateral ocular cataracts, type 2 diabetes mellitus, hypogonadism, skin ulcers, and osteoporosis in the 30s. Myocardial infarction and cancer are the most common causes of death; the mean age of death in individuals with Werner syndrome is 54 years.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/12147">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_82798"><div><strong>Junctional epidermolysis bullosa, non-Herlitz type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>82798</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.">C0268374</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Junctional epidermolysis bullosa (JEB) is characterized by fragility of the skin and mucous membranes, manifest by blistering with little or no trauma. Blistering may be severe and granulation tissue can form on the skin around the oral and nasal cavities, fingers and toes, and internally around the upper airway. Blisters generally heal with no significant scarring. Broad classification of JEB includes JEB generalized severe and JEB generalized intermediate. In JEB generalized severe, blisters are present at birth or become apparent in the neonatal period. Congenital malformations of the urinary tract and bladder may also occur. In JEB generalized intermediate, the phenotype may be mild with blistering localized to hands, feet, knees, and elbows with or without renal or ureteral involvement. Some individuals never blister after the newborn period. Additional features shared by JEB and the other major forms of epidermolysis bullosa (EB) include congenital localized absence of skin (aplasia cutis congenita), milia, nail dystrophy, scarring alopecia, hypotrichosis, pseudosyndactyly, and other contractures.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/82798">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_208666"><div><strong>Odonto-onycho-dermal dysplasia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>208666</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.">C0796093</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Odontoonychodermal dysplasia (OODD) is an autosomal recessive disorder characterized by dry hair, severe hypodontia, smooth tongue with marked reduction of fungiform and filiform papillae, onychodysplasia, hyperkeratosis of the palms and soles, hypo- and hyperhidrosis of the skin, and atrophic patches on the face (summary by Adaimy et al., 2007; Yu et al., 2019).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/208666">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_388129"><div><strong>Poikiloderma with neutropenia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>388129</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.">C1858723</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Poikiloderma with neutropenia (PN) is characterized by an inflammatory eczematous rash (appears at ages 6-12 months) followed by post-inflammatory poikiloderma (at age >2 years) and chronic noncyclic neutropenia typically associated with recurrent sinopulmonary infections in the first two years of life and (often) bronchiectasis. There is increased risk for myelodysplastic syndrome, acute myelogenous leukemia, and skin cancer. Other ectodermal findings include thickened nails, nail dystrophy, and palmar/plantar hyperkeratosis. Most affected individuals also have reactive airway disease, and some have short stature, hypogonadotropic hypogonadism, midfacial retrusion, calcinosis cutis, and non-healing skin ulcers.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/388129">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_811523"><div><strong>Pachyonychia congenita 3</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>811523</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.">C3714948</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Pachyonychia congenita (PC) is characterized by hypertrophic nail dystrophy, painful palmoplantar keratoderma and blistering, oral leukokeratosis, pilosebaceous cysts (including steatocystoma and vellus hair cysts), palmoplantar hyperhydrosis, and follicular keratoses on the trunk and extremities.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/811523">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_816724"><div><strong>Palmoplantar keratoderma, nonepidermolytic, focal or diffuse</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>816724</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.">C3810394</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Pachyonychia congenita (PC) is characterized by hypertrophic nail dystrophy, painful palmoplantar keratoderma and blistering, oral leukokeratosis, pilosebaceous cysts (including steatocystoma and vellus hair cysts), palmoplantar hyperhydrosis, and follicular keratoses on the trunk and extremities.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/816724">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_906476"><div><strong>Epidermolysis bullosa simplex with nail dystrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>906476</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.">C4225309</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive generalized intermediate epidermolysis bullosa simplex 5D (EBS5D) is characterized by generalized skin blistering that heals with scarring and hyperpigmentation. Nail dystrophy is severe. Mucous membranes, heart, and muscle are spared (Gostynska et al., 2015). For a discussion of genetic heterogeneity of the subtypes of EBS, see EBS1A (131760).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/906476">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_930338"><div><strong>Autosomal dominant palmoplantar keratoderma and congenital alopecia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>930338</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.">C4304669</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Palmoplantar keratoderma and congenital alopecia-1 (PPKCA1) is a rare autosomal dominant disorder characterized by severe hyperkeratosis and congenital alopecia. Nail changes occur in some patients (summary by Castori et al., 2010). Also see PPKCA2 (212360), an autosomal recessive disorder characterized by congenital alopecia and progressive hyperkeratosis resulting in sclerodactyly, severe contractures and tapering of the digits, and pseudoainhum formation.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/930338">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1053126"><div><strong>Epidermolytic palmoplantar keratoderma, 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1053126</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier assigned by MedGen (starting with CN) for terms that cannot be identified in NLM's Unified Medical Language system (UMLS) Click for more information.">CN377798</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Epidermolytic palmoplantar keratoderma-1 (EPPK1) is an autosomal dominant skin disorder characterized clinically by diffuse, yellow thickening of the skin of the palms and soles. There is no extension of the keratoderma to dorsal surfaces of hands and feet, inner wrists, and Achilles tendon area (transgrediens). Knuckle pads may be present in some individuals (summary by Kuster et al., 2002, Chiu et al., 2007). Genetic Heterogeneity of Epidermolytic Palmoplantar Keratoderma Epidermolytic palmoplantar keratoderma-2 (EPPK2; 620411) is caused by mutation in the keratin-1 gene (KRT1; 139350) on chromosome 12q13. Classification of Palmoplantar Keratoderma PPK has been classified into diffuse, focal, and punctate forms according to the pattern of hyperkeratosis on the palms and soles (Lucker et al., 1994). Diffuse PPK develops at birth or shortly thereafter and involves the entire palm and sole with a sharp cutoff at an erythematous border; there are no lesions outside the volar skin, and, in particular, no follicular or oral lesions. In contrast, focal PPK is a late-onset form in which focal hyperkeratotic lesions develop in response to mechanical trauma; an important distinguishing feature is the presence of lesions at other body sites, e.g., oral and follicular hyperkeratosis (Stevens et al., 1996). Palmoplantar keratodermas can be further subdivided histologically into epidermolytic and nonepidermolytic PPK (Risk et al., 1994). Genetic Heterogeneity of Palmoplantar Keratoderma Nonepidermolytic palmoplantar keratoderma (NEPPK; 600962) is caused by mutation in the KRT1 gene. A focal form of NEPPK (FNEPPK1; 613000) is caused by mutation in the KRT16 gene (148067). Another focal form, FNEPPK2 (616400), is caused by mutation in the TRPV3 gene (607066); mutation in TRPV3 can also cause Olmsted syndrome (OLMS; 614594), a severe mutilating form of PPK. The diffuse Bothnian form of NEPPK (PPKB; 600231) is caused by mutation in the AQP5 gene (600442). The Nagashima type of nonepidermolytic diffuse PPK (PPKN; 615598) is caused by mutation in the SERPINB7 gene (603357). A generalized form of epidermolytic hyperkeratosis (EHK; 113800), also designated bullous congenital ichthyosiform erythroderma (BCIE), is caused by mutation in the keratin genes KRT1 and KRT10 (148080). For a discussion of punctate PPK, see 148600; for a discussion of striate PPK, see 148700.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1053126">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_930338" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal dominant palmoplantar keratoderma and congenital alopecia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_906476" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Epidermolysis bullosa simplex with nail dystrophy</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1053126" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Epidermolytic palmoplantar keratoderma, 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_82798" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Junctional epidermolysis bullosa, non-Herlitz type</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_208666" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Odonto-onycho-dermal dysplasia</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (9)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_811523" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pachyonychia congenita 3</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_816724" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Palmoplantar keratoderma, nonepidermolytic, focal or diffuse</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_388129" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Poikiloderma with neutropenia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_12147" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Werner syndrome</a></div></span></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35245567">Genotype-phenotype correlations of neurovascular structures on the feet in patients with pachyonychia congenita: A cross-sectional study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tan XL,
|
||
Thomas BR,
|
||
Steele L,
|
||
Schwartz J,
|
||
Hansen CD,
|
||
O'Toole EA</span><br />
|
||
<span class="medgenPMjournal">J Am Acad Dermatol</span>
|
||
2022 Nov;87(5):1172-1174.
|
||
Epub 2022 Mar 2
|
||
doi: 10.1016/j.jaad.2022.02.050.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35245567" target="_blank">35245567</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19067694">Differential diagnosis of plantar wart from corn, callus and healed wart with the aid of dermoscopy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bae JM,
|
||
Kang H,
|
||
Kim HO,
|
||
Park YM</span><br />
|
||
<span class="medgenPMjournal">Br J Dermatol</span>
|
||
2009 Jan;160(1):220-2.
|
||
Epub 2008 Nov 28
|
||
doi: 10.1111/j.1365-2133.2008.08937.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19067694" target="_blank">19067694</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1387356">Simple management of plantar clavi.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sheard C</span><br />
|
||
<span class="medgenPMjournal">Cutis</span>
|
||
1992 Aug;50(2):138.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1387356" target="_blank">1387356</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(plantar%20hyperkeratosis)%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 (26)</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/37128833">Dermatoses in overweight and obese children and their relationship with insulin and skin color.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kus MM,
|
||
Mulayim MK,
|
||
Kus C,
|
||
Doganer A,
|
||
Ozturk P,
|
||
Temiz F,
|
||
Nazik H</span><br />
|
||
<span class="medgenPMjournal">J Cosmet Dermatol</span>
|
||
2023 Oct;22(10):2791-2798.
|
||
Epub 2023 May 2
|
||
doi: 10.1111/jocd.15773.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37128833" target="_blank">37128833</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31610857">Skin changes in the obese patient.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hirt PA,
|
||
Castillo DE,
|
||
Yosipovitch G,
|
||
Keri JE</span><br />
|
||
<span class="medgenPMjournal">J Am Acad Dermatol</span>
|
||
2019 Nov;81(5):1037-1057.
|
||
doi: 10.1016/j.jaad.2018.12.070.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31610857" target="_blank">31610857</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21564065">Obesity and the skin.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shipman AR,
|
||
Millington GW</span><br />
|
||
<span class="medgenPMjournal">Br J Dermatol</span>
|
||
2011 Oct;165(4):743-50.
|
||
doi: 10.1111/j.1365-2133.2011.10393.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21564065" target="_blank">21564065</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16799182">An overview of dermatological conditions commonly associated with the obese patient.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hahler B</span><br />
|
||
<span class="medgenPMjournal">Ostomy Wound Manage</span>
|
||
2006 Jun;52(6):34-6, 38, 40 passim.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16799182" target="_blank">16799182</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15475230">Obesity and dermatology.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Scheinfeld NS</span><br />
|
||
<span class="medgenPMjournal">Clin Dermatol</span>
|
||
2004 Jul-Aug;22(4):303-9.
|
||
doi: 10.1016/j.clindermatol.2004.01.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15475230" target="_blank">15475230</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Plantar%20hyperkeratosis%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 (43)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32052849">A Family with Palmar and Plantar Hyperkeratosis: A Quiz.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Juratli HA,
|
||
Jägle S,
|
||
Happle R,
|
||
Avci P,
|
||
Didona D,
|
||
Fischer J</span><br />
|
||
<span class="medgenPMjournal">Acta Derm Venereol</span>
|
||
2020 Feb 27;100(4):adv00064.
|
||
doi: 10.2340/00015555-3419.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32052849" target="_blank">32052849</a><a href="/pmc/articles/PMC9128890" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31610857">Skin changes in the obese patient.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hirt PA,
|
||
Castillo DE,
|
||
Yosipovitch G,
|
||
Keri JE</span><br />
|
||
<span class="medgenPMjournal">J Am Acad Dermatol</span>
|
||
2019 Nov;81(5):1037-1057.
|
||
doi: 10.1016/j.jaad.2018.12.070.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31610857" target="_blank">31610857</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15475230">Obesity and dermatology.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Scheinfeld NS</span><br />
|
||
<span class="medgenPMjournal">Clin Dermatol</span>
|
||
2004 Jul-Aug;22(4):303-9.
|
||
doi: 10.1016/j.clindermatol.2004.01.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15475230" target="_blank">15475230</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11451323">Atypical familial Papillon-Lefèvre syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Inalöz HS,
|
||
Harman M,
|
||
Akdeniz S,
|
||
Inalöz SS,
|
||
Isik AG</span><br />
|
||
<span class="medgenPMjournal">J Eur Acad Dermatol Venereol</span>
|
||
2001 Jan;15(1):48-50.
|
||
doi: 10.1046/j.1468-3083.2001.00121.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11451323" target="_blank">11451323</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/590036">Porokeratosis plantaris discreta.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Montgomery RM</span><br />
|
||
<span class="medgenPMjournal">Cutis</span>
|
||
1977 Dec;20(6):711-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/590036" target="_blank">590036</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Plantar%20hyperkeratosis%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/30372722">Vemurafenib-induced plantar hyperkeratosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bashline BR,
|
||
Bedocs PM</span><br />
|
||
<span class="medgenPMjournal">Cutis</span>
|
||
2018 Sep;102(3):E19-E21.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30372722" target="_blank">30372722</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29799097">Cutaneous toxicities of new treatments for melanoma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Boada A,
|
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Carrera C,
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Segura S,
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Collgros H,
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Pasquali P,
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<span class="bold">PMID: </span><a href="/pubmed/29799097" target="_blank">29799097</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/21564065">Obesity and the skin.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Shipman AR,
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2011 Oct;165(4):743-50.
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<div class="nl"><a target="_blank" href="/pubmed/16800355">Papillon Lefevre syndrome.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Dhadke SV,
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Kulkarni PM,
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<div class="nl"><a target="_blank" href="/pubmed/7239745">Plantar and palmar hyperkeratosis in young castrated women.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Wachtel TJ</span><br />
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<span class="medgenPMjournal">Int J Dermatol</span>
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1981 May;20(4):270-1.
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doi: 10.1111/j.1365-4362.1981.tb04335.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7239745" target="_blank">7239745</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Plantar%20hyperkeratosis%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 (29)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37268490">Correlation between the foot pressure index and the prevalence of plantar hyperkeratosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sánchez-Rodríguez R,
|
||
Martínez-Quintana R,
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Martínez-Nova A,
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Martínez-Rico M,
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Pedrera-Zamorano JD,
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Chicharro-Luna E</span><br />
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<span class="medgenPMjournal">J Tissue Viability</span>
|
||
2023 Aug;32(3):401-405.
|
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Epub 2023 May 29
|
||
doi: 10.1016/j.jtv.2023.05.007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37268490" target="_blank">37268490</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33084262">Sézary Syndrome: a clinico-pathological study of 9 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bolcato V,
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Barruscotti S,
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DE Silvestri A,
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Tomasini CF,
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Brazzelli V</span><br />
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<span class="medgenPMjournal">Ital J Dermatol Venerol</span>
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2021 Feb;156(1):73-83.
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Epub 2020 Oct 21
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doi: 10.23736/S2784-8671.19.06403-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33084262" target="_blank">33084262</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16012214">Prosthodontic rehabilitation in Papillon-Lefevre syndrome: a case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jain V,
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Gupta R,
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Parkash H</span><br />
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<span class="medgenPMjournal">J Indian Soc Pedod Prev Dent</span>
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2005 Jun;23(2):96-8.
|
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doi: 10.4103/0970-4388.16451.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16012214" target="_blank">16012214</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15475230">Obesity and dermatology.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Scheinfeld NS</span><br />
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||
<span class="medgenPMjournal">Clin Dermatol</span>
|
||
2004 Jul-Aug;22(4):303-9.
|
||
doi: 10.1016/j.clindermatol.2004.01.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15475230" target="_blank">15475230</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9443100">Cowden's disease--a report on the first case in Korea and literature review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lee HR,
|
||
Moon YS,
|
||
Yeom CH,
|
||
Kim KW,
|
||
Chun JY,
|
||
Kim HK,
|
||
Choi HS,
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||
Kim DK,
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Chung TS</span><br />
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<span class="medgenPMjournal">J Korean Med Sci</span>
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1997 Dec;12(6):570-5.
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||
doi: 10.3346/jkms.1997.12.6.570.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9443100" target="_blank">9443100</a><a href="/pmc/articles/PMC3054322" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Plantar%20hyperkeratosis%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 (20)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37268490">Correlation between the foot pressure index and the prevalence of plantar hyperkeratosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sánchez-Rodríguez R,
|
||
Martínez-Quintana R,
|
||
Martínez-Nova A,
|
||
Martínez-Rico M,
|
||
Pedrera-Zamorano JD,
|
||
Chicharro-Luna E</span><br />
|
||
<span class="medgenPMjournal">J Tissue Viability</span>
|
||
2023 Aug;32(3):401-405.
|
||
Epub 2023 May 29
|
||
doi: 10.1016/j.jtv.2023.05.007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37268490" target="_blank">37268490</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9714984">Pachyonychia congenita associated with steatocystoma multiplex.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kim JU,
|
||
Nogita T,
|
||
Terajima S,
|
||
Kawashima M</span><br />
|
||
<span class="medgenPMjournal">J Dermatol</span>
|
||
1998 Jul;25(7):479-81.
|
||
doi: 10.1111/j.1346-8138.1998.tb02439.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9714984" target="_blank">9714984</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2140447">Pachyonychia congenita: a clinical study of 12 cases and review of the literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Su WP,
|
||
Chun SI,
|
||
Hammond DE,
|
||
Gordon H</span><br />
|
||
<span class="medgenPMjournal">Pediatr Dermatol</span>
|
||
1990 Mar;7(1):33-8.
|
||
doi: 10.1111/j.1525-1470.1990.tb01070.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2140447" target="_blank">2140447</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2932504">Plantar hyperkeratosis: a study of callosities and normal plantar skin.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Thomas SE,
|
||
Dykes PJ,
|
||
Marks R</span><br />
|
||
<span class="medgenPMjournal">J Invest Dermatol</span>
|
||
1985 Nov;85(5):394-7.
|
||
doi: 10.1111/1523-1747.ep12277052.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2932504" target="_blank">2932504</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7239745">Plantar and palmar hyperkeratosis in young castrated women.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wachtel TJ</span><br />
|
||
<span class="medgenPMjournal">Int J Dermatol</span>
|
||
1981 May;20(4):270-1.
|
||
doi: 10.1111/j.1365-4362.1981.tb04335.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7239745" target="_blank">7239745</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Plantar%20hyperkeratosis%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 (33)</a></div></div>
|
||
</div>
|
||
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|
||
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|
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|
||
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|
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<div class="supplemental col three_col last">
|
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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=(plantar%20hyperkeratosis)%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=67d5a25167c23b31e00574b9">Plantar hyperkeratosis</a>
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<div class="ralinkpop offscreen_noflow">Plantar hyperkeratosis<div class="brieflinkpopdesc"></div></div>
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