Report of two unrelated families with Jalili syndrome and a novel nonsense heterozygous mutation in CNNM4 gene

• Published in: European journal of medical genetics Vol. 61; no. 7; pp. 384 - 387
• Main Authors: Maia, Célia Márcia Fernandes, Machado, Renato Assis, Gil-da-Silva-Lopes, Vera Lúcia, Lustosa-Mendes, Elaine, Rim, Priscila Hae Hyun, Dias, Verônica Oliveira, Martelli, Daniella Reis Barbosa, Nasser, Luciano Sólia, Coletta, Ricardo D., Martelli-Júnior, Hercílio
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Masson SAS 01-07-2018
• Subjects: Amelogenesis imperfecta; CNNM4; Cone-rod dystrophy; Jalili syndrome; Mutation; Mutation; Amelogenesis imperfecta; Cone-rod dystrophy; CNNM4; Jalili syndrome
• ISSN: 1769-7212; 1878-0849
• DOI: 10.1016/j.ejmg.2018.02.003

Jalili syndrome (JS) is an autosomal recessive disease characterized by a combination of cone-rode retinal dytrophy (CRD) and amelogenesis imperfect (AI). Mutations in cyclin and CBS domain divalent metal cation transport mediator 4 (CNNM4) gene cause JS. Here we described 2 families (3 members) affected by JS. In the first family, JS was caused by the homozygous p.Leu324Pro (c.971T > C) missense mutation and the affected patient developed both CRD and AI. In the second family, a specific combination of a compound heterozygous mutation was found – the p.Leu324Pro (c.971T > C) missense transition and the novel p.Tyr581* (c.1743C > G) nonsense mutation. The proband showed CRD and AI, but her father just developed eye alterations. Together, these findings suggest that the p.Leu324Pro mutation in homozygosis induces a complete phenotype with both CRD and AI, but in heterozygosis and in composition with the novel p.Tyr581* nonsense mutation in CNNM4 promotes variable clinical expressivity, particularly with lack of dental phenotypes. These different phenotypes could be explained by deletions affecting the proband's homologous allele, epistasia or interactions with environmental factors leading to residual activity of protein.