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KIAA2022 nonsense mutation in a symptomatic female
Author(s) -
Farach Laura S.,
Northrup Hope
Publication year - 2016
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.37479
Subject(s) - nonsense , intellectual disability , nonsense mutation , microcephaly , genetics , phenotype , mutation , genetic counseling , short stature , biology , epilepsy , genotype , gene , genotype phenotype distinction , missense mutation , endocrinology , neuroscience
Mutations in the KIAA2022 gene have been implicated in non‐syndromic X‐linked intellectual disability. Thus far, all carrier females reported have been unaffected and genotype–phenotype correlations have not been described. Herein, we report a de novo KIAA2022 nonsense mutation in a 17‐year‐old female with short stature, microcephaly, severe intellectual disability, poor speech, epilepsy, and autistic behavior. X‐inactivation pattern is normal suggesting that the mutation is causing the phenotype. This report contests the current view that KIAA2022 mutations only affect males, which has implications for testing and genetic counseling. © 2015 Wiley Periodicals, Inc.