Biotinidase Deficiency Accompanying Hair Changes and Periorificial Lesions: A Case Report
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Tarih
2011
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Galenos Yayincilik
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Biotinidase deficiency is impairment of biotin metabolism characterized by various dermatological, ophthalmic and neurological symptoms. Autosomal recessive trait is a disorder. Skin findings such as alopecia, periorificial dermatitis and seborrhoeic dermatitis lesions are seen. Clinical signs improved dramatically with biotine treatment. We presented a 6-year-old male patient with periorificial lesions, alopecia and microscopic hair shaft defects.
Açıklama
Anahtar Kelimeler
Alopecia, Biotin, Biotinidase Deficiency, Periorificial Dermatitis
Kaynak
Turk Dermatoloji Dergisi-Turkish Journal of Dermatology
WoS Q Değeri
N/A
Scopus Q Değeri
Q4
Cilt
5
Sayı
3
