Autosomal recessive hypohidrotic ectodermal dysplasia (Q87150): Difference between revisions

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Displasia ectodérmica hipoidrótica ou anidrótica é uma síndrome de displasia ectodérmica caracterizada por sudação diminuída ou ausente, intolerância ao calor, cabelo seco e esparso, pele muito fina, ausência total ou parcial de dentes, dismorfismo facial característico, todos estes frequentemente associados a transtornos oculares, digestivos ou pulmonares.
description / endescription / en
 
Ectodermal hypohidrotic or anhidrotic dysplasia is an ectodermal dysplasia syndrome characterised by decreased or absent sudation, intolerance to heat, dry, sparse hair, very fine skin, total or partial lack of teeth, characteristic facial dysmorphism, all of which are often associated with ocular, digestive, or pulmonary disorders.
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Property / Canonical URI: https://id.who.int/icd/entity/7083042 / rank
 
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Property / CURIE
 
CID11:ID_7083042
Property / CURIE: CID11:ID_7083042 / rank
 
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dki-india-ID_7083042
Property / Canary Token: dki-india-ID_7083042 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 12:43, 15 August 2026

Ectodermal hypohidrotic or anhidrotic dysplasia is an ectodermal dysplasia syndrome characterised by decreased or absent sudation, intolerance to heat, dry, sparse hair, very fine skin, total or partial lack of teeth, characteristic facial dysmorphism, all of which are often associated with ocular, digestive, or pulmonary disorders.
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ID_7083042
    English
    Autosomal recessive hypohidrotic ectodermal dysplasia
    Ectodermal hypohidrotic or anhidrotic dysplasia is an ectodermal dysplasia syndrome characterised by decreased or absent sudation, intolerance to heat, dry, sparse hair, very fine skin, total or partial lack of teeth, characteristic facial dysmorphism, all of which are often associated with ocular, digestive, or pulmonary disorders.

      Statements

      CID11:ID_7083042
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      dki-india-ID_7083042
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      Concluído
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      13 August 2026
      0 references