Chromosome 15q Deletion Overview
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Learn About Chromosome 15q Deletion
What is the definition of Chromosome 15q Deletion?
Chromosome 15q deletion is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the long arm (q) of chromosome 15. The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved. Features that often occur in people with Chromosome 15q deletion include developmental delay, intellectual disability, behavioral problems, and distinctive facial features. Most cases are not inherited, but people can pass the deletion on to their children.
What are the alternative names for Chromosome 15q Deletion?
- Chromosome 15q deletion
- 15q deletion
- 15q monosomy
- Deletion 15q
- Monosomy 15q
- Partial monosomy 15q
Who are the top Chromosome 15q Deletion Local Doctors?
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What are the latest Chromosome 15q Deletion Clinical Trials?
Promoting Prosocial Behavior in Syndromic Intellectual and Developmental Disabilities
Enrollment Status: Recruiting
Publish Date: January 31, 2025
Intervention Type: Behavioral, Other
Study Phase: Not Applicable
Summary: The purpose of this study is to evaluate the effectiveness of an adapted, telehealth functional behavioral therapy (FBTsIDD) specifically focused on promoting appropriate communication and behavioral strategies in individuals with syndromic intellectual and developmental disorders. Participants will be asked to complete virtual study assessments at intake and then on a monthly basis for the durati...
Who are the sources who wrote this article ?
Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center
What are the Latest Advances for Chromosome 15q Deletion?
A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature.
Journal: BMC medical genomics
Published: December 06, 2019
Compulsions in Prader-Willi syndrome: occurrence and severity as a function of genetic subtype.
Journal: Actas espanolas de psiquiatria
Published: May 01, 2019
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Apparent germline mosaicism for a 15q11-q13 deletion causing recurrent Angelman syndrome in a Chinese family.
Journal: European journal of obstetrics, gynecology, and reproductive biology
Published: January 16, 2019