Irreversibility of Symptoms with Biotin Therapy in an Adult with Profound Biotinidase Deficiency

Author:

Ferreira Patrick,Chan Alicia,Wolf Barry

Publisher

Springer Berlin Heidelberg

Reference8 articles.

1. Bottin L, Prud'hon S, Guey S, Giannesini C, Wolf B, Pindoliua K, Stankoff B (2015) Biotinidase deficiency mimicking neuromyelitis optica: initially exhibiting symptoms in adulthood. Mult Scler J 21:1604–1607

2. Pispa J (1965) Animal biotinidase. Ann Med Exp Biol Fenn 43(Suppl.5):1–39

3. Wolf B (2001) Disorders of biotin metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease. McGraw-Hill, New York, pp 3935–3962

4. Wolf B (2012) Biotinidase deficiency: if you have to have an inherited metabolic disease, this is the one to have. Gend Med 14:565–575

5. Wolf B (2015a) Biotinidase deficiency should be considered in individuals exhibiting myelopathy with or without vision loss. Mol Genet Metab 116:113–118

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