Choudhary Ankita, Pandya Rutvi M, Joshi Rima, Shah Bela J
Department of Dermatology, B.J. Medical College, Civil Hospital, Ahmedabad, Gujarat, India.
Indian Dermatol Online J. 2022 Sep 21;14(2):237-239. doi: 10.4103/idoj.idoj_322_22. eCollection 2023 Mar-Apr.
Biotinidase deficiency (BD) is a rare autosomal recessive, vitamin-responsive inborn error of metabolism associated with a wide spectrum of dermatological, neurological, auditory, and metabolic abnormalities. This case report reiterates that a high index of suspicion in childhood diseases with periorificial desquamation can lead to timely detection and active intervention in BD.
生物素酶缺乏症(BD)是一种罕见的常染色体隐性遗传性、维生素反应性先天性代谢紊乱疾病,与多种皮肤、神经、听觉和代谢异常有关。本病例报告重申,对患有口周脱屑的儿童疾病保持高度怀疑指数可导致对生物素酶缺乏症的及时检测和积极干预。