J Korean Child Neurol Soc.  2010 Nov;18(2):332-337.

A Case of Walker-Warburg Syndrome Presented with Seizures

Affiliations
  • 1Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, Korea. iglee@catholic.ac.kr

Abstract

Walker-Warburg syndrome (WWS) is a rare autosomal recessive disorder characterized by congenital muscular dystrophy, brain (lissencephaly, hydrocephalus, cerebellar malformations) and retinal abnormalities, and is associated with mental retardation and seizures. In 1942, Walker was the first to report a case of WWS. As Fukuyama congenital muscular dystrophy or muscle-eye-brain disorder, it has been demonstrated that the glycosylation defects of alpha-dystroglycan which take a great role in muscle and neuron regeneration are at the root of these disorders. We report a five months old male patient who was presented with seizures as the chief complaint and was diagnosed with WWS, based on clinical criteria, MRI, muscular biopsy, ocular examination, and laboratory findings.

Keyword

Muscular dystrophies; Lissencephaly

MeSH Terms

Biopsy
Brain
Dystroglycans
Glycosylation
Humans
Hydrocephalus
Intellectual Disability
Lissencephaly
Male
Muscles
Muscular Dystrophies
Neurons
Regeneration
Retinaldehyde
Seizures
Walker-Warburg Syndrome
Dystroglycans
Retinaldehyde
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