Literature DB >> 3783319

Multiple carboxylase deficiency due to deficiency of biotinidase.

L P Thuy, B Zielinska, E Zammarchi, E Pavari, A Vierucci, F Sweetman, L Sweetman, W L Nyhan.   

Abstract

A patient with biotinidase deficiency was studied in whom the first admission to hospital for acidosis occurred at 5 years of age. Sensorineural abnormalities of the optic and auditory nerves antedated diagnosis and treatment with biotin, and these sensory losses did not resolve with treatment. The other clinical manifestations of the disease were highly responsive to biotin. Biotinidase was assayed using 14C-labeled natural substrate. The activity in the patient approximated 1% of the control level.

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Year:  1986        PMID: 3783319     DOI: 10.3109/01677068609106859

Source DB:  PubMed          Journal:  J Neurogenet        ISSN: 0167-7063            Impact factor:   1.250


  2 in total

1.  Cerebral metabolic change after treatment in biotinidase deficiency.

Authors:  I T Lott; S Lottenberg; W L Nyhan; M J Buchsbaum
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

2.  Outcomes of oral biotin treatment in patients with biotinidase deficiency - Twenty years follow-up.

Authors:  Edyta Szymańska; Małgorzata Średzińska; Agnieszka Ługowska; Magdalena Pajdowska; Dariusz Rokicki; Anna Tylki-Szymańska
Journal:  Mol Genet Metab Rep       Date:  2015-10-06
  2 in total

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