| Literature DB >> 24066991 |
Sujatha Jagadeesh1, Beena Suresh, Suresh Seshadri, Yoichi Suzuki.
Abstract
Biotinidase deficiency is a rare metabolic disorder which can cause dermatological manifestations and lead to severe neurological sequelae if untreated. Holocarboxylase synthetase deficiency also has similar manifestations and needs to be differentiated. We present a neonate who had atypical early onset symptoms and was diagnosed to have biotinidase deficiency. Copyright 2012, NMJI.Entities:
Mesh:
Year: 2013 PMID: 24066991
Source DB: PubMed Journal: Natl Med J India ISSN: 0970-258X Impact factor: 0.537