Neuropediatrics 2005; 36(3): 223-226
DOI: 10.1055/s-2005-865715
Short Communication

Georg Thieme Verlag KG Stuttgart · New York

Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum (H-ABC). Report of a New Case

S. Mercimek-Mahmutoglu1 , M. S. van der Knaap2 , I. Baric3 , D. Prayer4 , S. Stoeckler-Ipsiroglu1
  • 1Department of Pediatrics, University of Vienna, Vienna, Austria (location where research was carried out)
  • 2Department of Child Neurology, VU University Medical Center, Amsterdam, The Netherlands
  • 3Department of Pediatrics, University Center, Zagreb, Croatia
  • 4Department of Neuroradiology, University of Vienna, Vienna, Austria
Further Information

Publication History

Received: December 27, 2004

Accepted after Revision: May 1, 2005

Publication Date:
09 June 2005 (online)

Abstract

Hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC) syndrome is a new neurodegenerative entity, which was first described by van der Knaap in 2002 in 7 patients aged from 2 months to 2 years. We describe a new, 42-month-old female patient who developed progressive dystonia, spasticity and oculogyric eye movements since the age of 3 months. The diagnosis was made by characteristic MRI findings including supratentorial hypomyelination and progressive atrophy of basal ganglia and cerebellum. Oculogyric eye movements have not been described in patients with H-ABC syndrome before. When compared with the normal age-related myelination patterns, the degree of hypomyelination increased progressively over the time course of 32 months, indicating arrest but not loss of myelination. The H-ABC syndrome adds to the differential diagnosis of progressive pyramidal and extrapyramidal movement disorders and to the increasing number of genetically determined hypomyelination syndromes.

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MD Sylvia Stoeckler-Ipsiroglu

Department of Pediatrics
Division Biochemical Diseases
British Columbia Children's Hospital

4480 Oak Street

Vancouver B. C. VGH 3V4

Canada

Email: sstoeckler@cw.bc.ca

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