A Case of IFAP Syndrome with Severe Atopic Dermatitis

Introduction. The IFAP syndrome is a rare X-linked genetic disorder characterized by the triad of follicular ichthyosis, atrichia, and photophobia. Case Report. A three-month-old Caucasian, male patient was observed with noncicatricial universal alopecia and persistent eczema from birth. He had dyst...

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Detalles Bibliográficos
Autores principales: Araújo, Catarina, Gonçalves-Rocha, Miguel, Resende, Cristina, Vieira, Ana Paula, Brito, Celeste
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320795/
https://www.ncbi.nlm.nih.gov/pubmed/25685152
http://dx.doi.org/10.1155/2015/450937

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320795/
https://www.ncbi.nlm.nih.gov/pubmed/25685152
http://dx.doi.org/10.1155/2015/450937

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