| Literature DB >> 2606126 |
M Steinlin1, E Boltshauser, B Steinmann, W Wichmann, G Niemeyer.
Abstract
We describe a 10-year-old boy with hyperprolinaemia type I and severe neurological abnormalities (mental retardation, cerebral palsy, epilepsy, nystagmus). Magnetic resonance imaging showed diffuse white matter involvement and electroretinography confirmed tapetoretinal degeneration. In view of reports in the literature, hyperprolinaemia type I may not be a benign condition, as usually assumed, but may lead to marked neurological abnormalities, particularly in affected males.Entities:
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Year: 1989 PMID: 2606126 DOI: 10.1007/bf02024332
Source DB: PubMed Journal: Eur J Pediatr ISSN: 0340-6199 Impact factor: 3.183