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