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A novel compound heterozygous mutation in TTC8 identified in a Japanese patient
Shigeru Sato1, Takeshi Morimoto1,2, Kikuko Hotta3
11Department of Ophthalmology, Osaka University Graduate School of Medicine, Osaka, Japan.
Abstract:
Bardet-Biedl syndrome (BBS), characterized by rod-cone dystrophy, postaxial polydactyly, central obesity, hypogonadism, renal abnormalities, and mental retardation, is a rare autosomal recessive disorder. To date, 21 causative genes have been reported. Here we describe a Japanese BBS patient with a novel compound heterozygous mutation in TTC8. To the best of our knowledge, this is the first description of a BBS patient with a mutation in the TTC8 gene in Japan.
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