Şenses, Dursun AliŞimşe, EnverYar, Neşe ErsözKeskin, MahmutKocabay, Kenan2024-09-252024-09-2520060010-0161https://hdl.handle.net/20.500.12491/12344Profound biotinidase deficiency was diagnosed in a 28-day old infant with seizures-like infantile spasms, alopecia and erythematous rash. Clinical signs improved dramatically with biotine treatment. Clinical features of biotinidase deficiency are discussed.trinfo:eu-repo/semantics/closedAccessBiotineBiotinidase deficiencyInfantile spasmsBiotinidase deficiency in a four-week-old infant with infantile spasmsİnfantil spazm şeklinde başlangiç gösteren biotinidaz eksikli?i]Article4921211242-s2.0-33745780119Q4