Medulloblastoma in a Child with the Metabolic Disease L-2-Hydroxyglutaric Aciduria

L-2-Hydroxyglutaric aciduria (LHGA) is a rare autosomal recessively inherited neurodegenerative disorder. It is characterized by psychomotor retardation, progressive ataxia and typical magnetic resonance imaging findings, and presents in early infancy. On the other hand, medulloblastomas are very co...

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Veröffentlicht in:	Pediatric neurosurgery 2002-07, Vol.37 (1), p.22-26
Hauptverfasser:	Özışık, Pınar Akdemir, Akalan, Nejat, Palaoğlu, Selçuk, Topçu, Meral
Format:	Artikel
Sprache:	eng
Schlagworte:	Aminoacid disorders Biological and medical sciences Brain Diseases, Metabolic, Inborn - complications Case Report Cerebellar Neoplasms - complications Cerebellar Neoplasms - diagnosis Child, Preschool Errors of metabolism Humans Hydroxy Acids - urine Male Medical sciences Medulloblastoma - complications Medulloblastoma - diagnosis Metabolic diseases Neurology Tumors of the nervous system. Phacomatoses
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