Literature DB >> 1384336

Behr's syndrome and 3-methylglutaconic aciduria.

R N Sheffer1, J Zlotogora, O N Elpeleg, J Raz, D Ben-Ezra.   

Abstract

We examined three patients from two families of Jewish-Iraqi origin who had progressive reduction of visual acuity and childhood onset of bilateral optic nerve atrophy without additional retinal abnormalities. They had neurologic symptoms compatible with Behr's syndrome. Neurologic signs included increased tendon reflexes, a positive Babinski sign, progressive spastic paraplegia, dysarthria, head nodding, and horizontal nystagmus. Neurologic involvement varied between affected siblings. The patients excreted excessive amounts of 3-methylglutaconic acid and 3-methylglutaric acid in their urine. We compared the characteristic ophthalmic features and the spectrum of neurologic signs encountered in this recently delineated autosomal recessive clinical entity with those of previously described entities associated with 3-methylglutaconic aciduria. Patients with early-onset optic atrophy should be examined for neurologic signs and screened for organic aciduria. A detailed ophthalmic examination is important in patients with neurologic abnormalities compatible with Behr's syndrome.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1384336     DOI: 10.1016/s0002-9394(14)71864-1

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  2 in total

1.  The Expanding MEGDEL Phenotype: Optic Nerve Atrophy, Microcephaly, and Myoclonic Epilepsy in a Child with SERAC1 Mutations.

Authors:  Heidi S Lumish; Yaping Yang; Fan Xia; Ashley Wilson; Wendy K Chung
Journal:  JIMD Rep       Date:  2014-07-06

2.  Behr's Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene.

Authors:  Angela Pyle; Venkateswaran Ramesh; Marina Bartsakoulia; Veronika Boczonadi; Aurora Gomez-Duran; Agnes Herczegfalvi; Emma L Blakely; Tania Smertenko; Jennifer Duff; Gail Eglon; David Moore; Patrick Yu-Wai-Man; Konstantinos Douroudis; Mauro Santibanez-Koref; Helen Griffin; Hanns Lochmüller; Veronika Karcagi; Robert W Taylor; Patrick F Chinnery; Rita Horvath
Journal:  J Neuromuscul Dis       Date:  2014
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.