Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2→q24.3 in a girl with autistic features and developmental delay

Chih Ping Chen*, Shuan Pei Lin, Schu Rern Chern, Yann Jang Chen, Fuu Jen Tsai, Pei Chen Wu, Wayseen Wang

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

We report a 3 years and 4 months old girl with autistic features, developmental delay, mental retardation, language impairment and dysmorphic features, carrying a 2.8 Mb de novo deletion of chromosome 2q24.2→q24.3 detected by array-CGH. This region contains two neuronal voltage-gated sodium channel genes SCN2A and SCN3A.

Original languageEnglish
Pages (from-to)217-220
Number of pages4
JournalEuropean Journal of Medical Genetics
Volume53
Issue number4
DOIs
StatePublished - Jul 2010

Fingerprint

Dive into the research topics of 'Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2→q24.3 in a girl with autistic features and developmental delay'. Together they form a unique fingerprint.

Cite this