J Mov Disord.  2016 May;9(2):120-123. 10.14802/jmd.16003.

Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation

Affiliations
  • 1Department of Neurology, Habib Bourguiba Hospital, Sfax, Tunisia. olfahdiji@yahoo.fr
  • 2Department of Neurology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

Abstract

Woodhouse-Sakati syndrome (WSS) is an infrequent autosomal recessive condition characterized by progressive extrapyramidal signs, mental retardation, hypogonadism, alopecia, and diabetes mellitus. This syndrome belongs to a heterogeneous group of inherited neurodegenerative disorders characterized iron accumulation in the brain, and it is caused by mutations of the C2orf37 gene. We report the first Tunisian family with two affected sisters presenting with a phenotype suggestive of WSS. We examined the index patient presenting with movement disorders and mental retardation and then searched for similar cases in her family, which identified a sister with similar signs. We performed a genetic study that confirmed the diagnosis and revealed a c.436delC mutation of the C2orf37 gene. Therefore, WSS is an important consideration in patients presenting with movement disorders and intellectual disability. A high consanguinity contributes to the clustering of such rare autosomal recessive syndromes.

Keyword

Woodhouse-Sakati syndrome; Dystonia; Mental retardation; Diabetes mellitus; Hypogonadism

MeSH Terms

Alopecia
Brain
Consanguinity
Diabetes Mellitus
Diagnosis
Dystonia
Humans
Hypogonadism
Intellectual Disability
Iron
Movement Disorders
Neurodegenerative Diseases
Phenotype
Siblings
Iron
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