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Clin Genet ; 92(1): 104-108, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27976805

RESUMO

We here report a family from Libya with three siblings suffering from early onset achalasia born to healthy parents. We analyzed roughly 5000 disease-associated genes by a next-generation sequencing (NGS) approach. In the analyzed sibling we identified two heterozygous variants in CRLF1 (cytokine receptor-like factor 1). Mutations in CRLF1 have been associated with autosomal recessive Crisponi or cold-induced sweating syndrome type 1 (CS/CISS1), which among other symptoms also manifests with early onset feeding difficulties. Segregation analysis revealed compound heterozygosity for all affected siblings, while the unaffected mother carried the c.713dupC (p.Pro239Alafs*91) and the unaffected father carried the c.178T>A (p.Cys60Ser) variant. The c.713dupC variant has already been reported in affected CS/CISS1 patients, the pathogenicity of the c.178T>A variant was unclear. As reported previously for pathogenic CRLF1 variants, cytokine receptor-like factor 1 protein secretion from cells transfected with the c.178T>A variant was severely impaired. From these results we conclude that one should consider a CRLF1-related disorder in early onset achalasia even if other CS/CISS1 related symptoms are missing.


Assuntos
Anormalidades Múltiplas/genética , Acalasia Esofágica/genética , Deformidades Congênitas da Mão/genética , Hiperidrose/genética , Receptores de Citocinas/genética , Trismo/congênito , Anormalidades Múltiplas/fisiopatologia , Morte Súbita , Acalasia Esofágica/fisiopatologia , Fácies , Predisposição Genética para Doença , Deformidades Congênitas da Mão/fisiopatologia , Sequenciamento de Nucleotídeos em Larga Escala , Homozigoto , Humanos , Hiperidrose/fisiopatologia , Mutação , Linhagem , Trismo/genética , Trismo/fisiopatologia
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