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izvor podataka: crosbi

Hypomylination and atrophy of the basal ganglia and cerebellum, a new syndrome:case report (CROSBI ID 739782)

Prilog sa skupa u časopisu | izvorni znanstveni rad

Mercimek-Mahmutoglu, S. ; Van der Knaap, M. ; Barić, Ivo ; Konstantopoulou, V. ; Prayer, D. ; Stoeckler-Ipsiroglu, S. Hypomylination and atrophy of the basal ganglia and cerebellum, a new syndrome:case report // Journal of inherited metabolic disease. 2004. str. 248-248-x

Podaci o odgovornosti

Mercimek-Mahmutoglu, S. ; Van der Knaap, M. ; Barić, Ivo ; Konstantopoulou, V. ; Prayer, D. ; Stoeckler-Ipsiroglu, S.

engleski

Hypomylination and atrophy of the basal ganglia and cerebellum, a new syndrome:case report

Introduction: Hypomylination and atrophy of the basal ganglia and cerebellum (H-ABC) syndrome in a newly described disease characterised by typical MRI changes. Clinical features include progressive pyramidal and extrapyramidal movement disorder, developmental retardation. The syndrome was described so far in 7 patients. Case report: This new patient was diagnosed at age of 3 years with H-ABC syndrome due to characteristic MRI changes and clinical features. Oculogyric crises were particulary remarkable. Application of our recently developed myelination score revealed progressive deviation of mylination from age related normal values (62% at age 8 months, and 30% at age 40 months). Discussion: The H-ABC syndrome represents a new differential diagnosis in patients with cerebral hypomyelination and should be considered particulary in patients after exclusion of Pelizaeus Merzbacher disease.

Hypomylination; Basal ganglia

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Podaci o prilogu

248-248-x.

2004.

nije evidentirano

objavljeno

Podaci o matičnoj publikaciji

Journal of inherited metabolic disease

0141-8955

Podaci o skupu

Nepoznat skup

ostalo

29.02.1904-29.02.2096

Povezanost rada

Kliničke medicinske znanosti

Indeksiranost