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.

References

  • 1 Aramideh M, Bour L J, Koelman J H, Speelman J D, Ongerboer de Visser B W. Abnormal eye movements in blepharospasm and involuntary levator palpebrae inhibition. Clinical and pathophysiological considerations.  Brain. 1994;  117 1457-1474
  • 2 Barkovich A J. Concepts of myelin and myelination in neuroradiology.  AJNR. 2000;  21 1099-1109
  • 3 Brautigam C, Steenbergen-Spanjers G C, Hoffmann G F, Dionisi-Vici C, van den Heuvel L P, Smeitink J A. et al . Biochemical and molecular genetic characteristics of the severe form of tyrosine hydroxylase deficiency.  Clin Chem. 1999;  45 2073-2078
  • 4 Clough C G, Plaitakis A, Yahr M D. Oculogyric crises and parkinsonism. A case of recent onset.  Arch Neurol. 1983;  40 36-37
  • 5 Korenke G C, Christen H J, Hyland K, Hunneman D H, Hanefeld F. Aromatic L-amino acid decarboxylase deficiency: an extrapyramidal movement disorder with oculogyric crises.  Eur J Paediatr Neurol. 1997;  1 67-71
  • 6 Nangaku M, Motoyoshi Y, Kwak S, Yoshikawa H, Iwata M. MRI pathology of the globus pallidus in a patient with oculogyric crisis and tremor.  Rinsho Shinkeigaku. 1990;  30 760-764
  • 7 Plecko B, Stockler-Ipsiroglu S, Gruber S, Mlynarik V, Moser E, Simbrunner J. et al . Degree of hypomyelination and magnetic resonance spectroscopy findings in patients with Pelizaeus-Merzbacher phenotype.  Neuropediatrics. 2003;  34 127-136
  • 8 Van der Knaap M S, Valk J. Magnetic Resonance of Myelin, Myelination and Myelin Disorders. Heidelberg; Springer Verlag 1995
  • 9 Van der Knaap M S, Naidu S, Pouwels P JW, Bonavita S, van Coster R, Lagae L. et al . New syndrome characterized by hypomyelination with atrophy of the basal ganglia and cerebellum.  Am J Neuroradiol. 2002;  23 1466-1474

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