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Alternating hemiplegia of childhood: a syndrome inherited with an autosomal dominant trait
Author(s) -
Kanavakis Emmanuel,
Xaidara Athina,
PapathanasiouKlontza Dimitra,
Velentza Stavroula,
Youroukos Sotiris
Publication year - 2003
Publication title -
developmental medicine and child neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.658
H-Index - 143
eISSN - 1469-8749
pISSN - 0012-1622
DOI - 10.1111/j.1469-8749.2003.tb00899.x
Subject(s) - magnetic resonance imaging , pediatrics , psychology , medicine , movement disorders , radiology , disease
Alternating hemiplegia of childhood is a rare disorder characterized by recurrent attacks of hemiplegia affecting either side of the body, oculomotor and autonomic disturbances, movement disorders, and progressive cognitive impairment. We report on one family with autosomal dominant alternating hemiplegia. The disorder was first recognized in a 9‐year‐old child, the third son of the family, who presented with learning disability,* tonic‐clonic seizures, dystonic attacks, and episodes of alternating hemiplegia starting at the age of 2 1 / 2 years. His mother and three brothers had similar symptoms. The maternal uncle, who has learning disability, had experienced multiple dystonic attacks. Tests performed on the family, including computerized tomography, magnetic resonance imaging, and magnetic resonance angiography of the brain as well as metabolic evaluation, were normal. Cytogenetic analysis was normal and mitochondrial DNA analysis revealed no deletions or mutations in the four affected family members and the grandmother. An autosomal dominant mode of inheritance is suggested by the fact that both sexes are affected in two generations.