Variants
Sign InSign Up

7q11.23 microduplication syndrome

Your Results

Sign In

Description

7q11.23 duplication syndrome is characterized by delayed motor, speech, and social skills in early childhood; neurologic abnormalities (hypotonia, adventitious movements, and abnormal gait and station); speech sound disorders including motor speech disorders (childhood apraxia of speech and/or dysarthria) and phonologic disorders; behavior problems including anxiety disorders (especially social anxiety disorder [social phobia]), selective mutism, attention-deficit/hyperactivity disorder, oppositional disorders, physical aggression, and autism spectrum disorder; and intellectual disability in some individuals. Distinctive facial features are common. Cardiovascular disease includes dilation of the ascending aorta. Approximately 30% of individuals have one or more congenital anomalies.

GeneReviews

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

0

Genes

    External Links

    • OMIM

      609757

    • Orphanet

      96121

    • HPO
    • Medgen

      C1857844

    © 2024 Biocodify. All rights reserved.

    TwitterTwitter

    Product

    HomePricingDashboard