Hypohidrotic ectodermal dysplasia: a case report

Hypohidrotic ectodermal dysplasia (HED) is a rare heterogeneous genetic congenital disorder affecting at least 1 in 5000–10,000 newborns. This disorder has a wide range of clinical manifestations; it affects organs originating from the embryonic ectoderm. CASE PRESENTATION: We present a case of a 2-...

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Detalles Bibliográficos
Autores principales: Albeik, Muhammad T. M. N., Abdullah, Lava, Almatroud, Muhammad M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010819/
https://www.ncbi.nlm.nih.gov/pubmed/36923780
http://dx.doi.org/10.1097/MS9.0000000000000240

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010819/
https://www.ncbi.nlm.nih.gov/pubmed/36923780
http://dx.doi.org/10.1097/MS9.0000000000000240

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