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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...
שמור ב:
| הוצא לאור ב: | Case Rep Med |
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| Main Authors: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Hindawi Publishing Corporation
2015
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4320795/ https://ncbi.nlm.nih.gov/pubmed/25685152 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/450937 |
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