A new phenotype of recessively inherited foveal hypoplasia and anterior segment dysgenesis maps to a locus on chromosome 16q23.2–24.2.

Ítems similars

• A new recessively inherited disorder composed of foveal hypoplasia, optic nerve decussation defects and anterior segment dysgenesis maps to chromosome 16q23.3-24.1
  per: Al-Araimi, Musallam, et al.
  Publicat: (2013)
• Unilateral foveal hypoplasia in a child with bilateral anterior segment dysgenesis
  per: Shields, Rebecca A, et al.
  Publicat: (2015)
• Recessive Mutations in SLC38A8 Cause Foveal Hypoplasia and Optic Nerve Misrouting without Albinism
  per: Poulter, James A., et al.
  Publicat: (2013)
• Congenital universal muscular hypoplasia: evidence for autosomal recessive inheritance.
  per: Pelias, M Z, et al.
  Publicat: (1979)
• Isolated foveal hypoplasia.
  per: Oliver, M D, et al.
  Publicat: (1987)