Comprehensive phenotyping of neuropsychiatric traits in a multiplex 3q29 deletion family: a case report

Comprehensive phenotyping of neuropsychiatric traits in a multiplex 3q29 deletion family: a case report

Abstract Background 3q29 deletion syndrome is associated with a range of medical, neurodevelopmental, and psychiatric phenotypes. The deletion is usually de novo but cases have been reported where the deletion is inherited from apparently unaffected parents. The presence of these unaffected or mildl...

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Bibliographic Details
Main Authors: Melissa M. Murphy, T. Lindsey Burrell, Joseph F. Cubells, Michael T. Epstein, Roberto Espana, Michael J. Gambello, Katrina Goines, Cheryl Klaiman, Sookyong Koh, Rossana Sanchez Russo, Celine A. Saulnier, Elaine Walker, The Emory 3q29 Project, Jennifer Gladys Mulle
Format: Article
Language:English
Published: BMC 2020-04-01
Series:BMC Psychiatry
Subjects:
3q29 deletion
Schizophrenia
Psychosis
ADHD
CNV disorder
Evaluation of genetic syndromes
Online Access:http://link.springer.com/article/10.1186/s12888-020-02598-w

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http://link.springer.com/article/10.1186/s12888-020-02598-w

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