Ectodermal dysplasia syndromes (Q46654): Difference between revisions

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Displasias ectodérmicas (DE) são um grupo heterogêneo de síndromes caracterizadas por distrofias do desenvolvimento de estruturas ectodérmicas, como hipoidrose, hipotricose, onicodisplasia e hipodontia ou anodontia. Mais de 160 síndromes de displasias ectodérmicas hereditárias clínica e geneticamente distintas foram catalogadas.
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Ectodermal dysplasias (EDs) are a heterogeneous group of syndromes characterised by developmental dystrophies of ectodermal structures, such as hypohidrosis, hypotrichosis, onychodysplasia and hypodontia or anodontia. More than 160 clinically and genetically distinct hereditary ectodermal dysplasia syndromes have been catalogued.

Revision as of 15:23, 13 August 2026

Ectodermal dysplasias (EDs) are a heterogeneous group of syndromes characterised by developmental dystrophies of ectodermal structures, such as hypohidrosis, hypotrichosis, onychodysplasia and hypodontia or anodontia. More than 160 clinically and genetically distinct hereditary ectodermal dysplasia syndromes have been catalogued.
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    Ectodermal dysplasia syndromes
    Ectodermal dysplasias (EDs) are a heterogeneous group of syndromes characterised by developmental dystrophies of ectodermal structures, such as hypohidrosis, hypotrichosis, onychodysplasia and hypodontia or anodontia. More than 160 clinically and genetically distinct hereditary ectodermal dysplasia syndromes have been catalogued.

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