Variants
Sign InSign Up

Anophthalmia/microphthalmia-esophageal atresia syndrome

Your Results

Sign In

Description

The phenotypic spectrum of SOX2 disorder includes anophthalmia and/or microphthalmia, brain malformations, developmental delay / intellectual disability, esophageal atresia, hypogonadotropic hypogonadism (manifest as cryptorchidism and micropenis in males, gonadal dysgenesis infrequently in females, and delayed puberty in both sexes), pituitary hypoplasia, postnatal growth delay, hypotonia, seizures, and spastic or dystonic movements.

GeneReviews

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

30

SEE THE VARIANTS →

Genes

External Links

  • OMIM

    206900

  • Orphanet

    77298

  • HPO
  • Medgen

    C1859773

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

The latest news and updates from Biocodify, sent to your inbox.