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Loss of function mutations in CTNNB1 have been reported in individuals with intellectual disability [MIM #615075] associated with peripheral spasticity, microcephaly and central hypotonia, suggesting a recognisable phenotype associated with haploinsufficiency for this gene. Trio based whole exome sequencing via the Deciphering Developmental Disorders (DDD) study has identified eleven further individuals with de novo loss of function mutations in CTNNB1. Here we report detailed phenotypic information on ten of these. We confirm the features that have been previously described and further delineate the skin and hair findings, including fair skin and fair and sparse hair with unusual patterning.

Original publication

DOI

10.1016/j.ejmg.2016.11.008

Type

Journal article

Journal

Eur J Med Genet

Publication Date

02/2017

Volume

60

Pages

130 - 135

Keywords

CTNNB1, Intellectual disability, Microcephaly, Adolescent, Adult, Child, Child, Preschool, Developmental Disabilities, Exome, Female, Haploinsufficiency, Humans, Intellectual Disability, Male, Microcephaly, Mutation, Phenotype, Sequence Analysis, DNA, beta Catenin