- 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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- Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution
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Jagota P, Ugawa Y, Aldaajani Z, Ibrahim NM, Ishiura H, Nomura Y, Tsuji S, Diesta C, Hattori N, Onodera O, Bohlega S, Al-Din A, Lim SY, Lee JY, Jeon B, Pal PK, Shang H, Fujioka S, Kukkle PL, Phokaewvarangkul O, Lin CH, Shambetova C, Bhidayasiri R
- KMID: 2545921
- J Mov Disord.
- 2023 Sep;16(3):231-247.
- doi: 10.14802/jmd.23065
Clinical case studies and reporting are important to the discovery of new disorders and the advancement of medical sciences. Both clinicians and basic scientists play equally important roles leading to... -
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