- Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation
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Hdiji O, Turki E, Bouzidi N, Bouchhima , Damak M, Bohlega S, Mhiri C
- KMID: 2308787
- J Mov Disord.
- 2016 May;9(2):120-123.
- doi: 10.14802/jmd.16003
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... -
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