Literature DB >> 15306966

[Optic neuropathy in biotinidase deficiency].

D Puertas Bordallo1, C Martín Reyes, M L Ruiz-Falcó Rojas, A Duat Rodríguez, M I Valls Ferrán.   

Abstract

CLINICAL CASE: We report a case of a 12 year old male with vision loss (0.1 in both eyes). He also had sensorineural hearing loss (cochlear implant), asthma, dermatitis and alopecia. He was diagnosed with retrobulbar optic neuropathy, and was started on a treatment of intravenous corticosteroids, showing no improvement. A screening for congenital metabolopathies revealed a biotinidase deficiency, and treatment with biotin achieved a rapid clinical improvement. DISCUSSION: When faced with an optic neuropathy in a child, we must always look for a biotinidase deficiency, because biotin therapy is the only treatment that achieves a clinical improvement.

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Year:  2004        PMID: 15306966     DOI: 10.4321/s0365-66912004000800007

Source DB:  PubMed          Journal:  Arch Soc Esp Oftalmol        ISSN: 0365-6691


  2 in total

Review 1.  Optic neuritis in pediatric population: a review in current tendencies of diagnosis and management.

Authors:  Rafael José Pérez-Cambrodí; Aránzazu Gómez-Hurtado Cubillana; María L Merino-Suárez; David P Piñero-Llorens; Carlos Laria-Ochaita
Journal:  J Optom       Date:  2014-02-18

2.  Optic neuritis in a child with biotinidase deficiency: case report and literature review.

Authors:  Abdul-Aziz Hayati; Wan-Hazabbah Wan-Hitam; Min-Tet Cheong; Rohaizan Yunus; Ismail Shatriah
Journal:  Clin Ophthalmol       Date:  2012-03-13
  2 in total

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