| Literature DB >> 27667191 |
Siham Chafai Elalaoui1, Nada Al-Sheqaih2, Ilham Ratbi3, Jill E Urquhart2, James O'Sullivan2, Sanjeev Bhaskar4, Simon S Williams4, Mustapha Elalloussi5, Jaber Lyahyai3, Leila Sbihi6, Imane Cherkaoui Jaouad7, Abdelhafid Sbihi8, William G Newman2, Abdelaziz Sefiani7.
Abstract
Raine syndrome is a rare autosomal recessive bone dysplasia characterized by characteristic facial features with exophthalmos and generalized osteosclerosis. Amelogenesis imperfecta, hearing loss, seizures, and intracerebral calcification are apparent in some affected individuals. Originally, Raine syndrome was originally reported as a lethal syndrome. However, recently a milder phenotype, compatible with life, has been described. Biallelic variants inFAM20C, encoding aGolgi casein kinase involved in biomineralisation, have been identified in affected individuals. We report here a consanguineous Moroccan family with two affected siblingsa girl aged 18 and a boy of 15years. Clinical features, including learning disability, seizures and amelogenesis imperfecta, initially suggested a diagnosis of Kohlschutter-Tonz syndrome. However,a novel homozygous FAM20Cvariantc.676T > A, p.(Trp226Arg) was identified in the affected siblings. Our report reinforces that Raine syndrome is compatible with life, and that mild hypophosphatemia and amelogenesis imperfecta are key features of the attenuated form.Entities:
Keywords: FAM20C gene; Kohlschutter-Tonz syndrome; Raine syndrome
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Year: 2016 PMID: 27667191 DOI: 10.1016/j.ejmg.2016.09.018
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.708