A Rare Case of Mainly Unilateral Focal Dermal Hypoplasia (Goltz Syndrome) in an Adult Male: A Case Report and Review of the Literature

Focal dermal hypoplasia (Goltz syndrome), is an exceedingly rare X-linked dominant genetic disorder. It is a multisystem disease, but it is hallmarked by characteristic skin changes. Focal dermal hypoplasia typically occurs in females (90%), and males are thought to only survive through having eithe...

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Detalles Bibliográficos
Autores principales: Lyons, Duncan, Rushton, Christopher, Sidhu, Sandeepal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383521/
https://www.ncbi.nlm.nih.gov/pubmed/34434364
http://dx.doi.org/10.14740/jmc3442

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383521/
https://www.ncbi.nlm.nih.gov/pubmed/34434364
http://dx.doi.org/10.14740/jmc3442

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