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Diagnosis and clinical presentation of two...
Journal article

Diagnosis and clinical presentation of two individuals with a rare TCF20 pathogenic variant

Abstract

TCF20-associated neurodevelopmental disorder (TAND) is a rare and phenotypically variable genetic condition. Common features include intellectual disability, neurobehavioural concerns, postnatal tall stature and hypotonia.Two unrelated early adolescent males were referred to genetics for assessment of developmental delay. The first male of Caucasian descent had a history of autism spectrum disorder (ASD), mitral valve prolapse and subtle …

Authors

Schneeweiss MR; Dale B; Ejaz R

Journal

BMJ Case Reports, Vol. 15, No. 12,

Publisher

BMJ

Publication Date

December 2022

DOI

10.1136/bcr-2022-248995

ISSN

1757-790X