Greig syndrome


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oc·u·lar hy·per·tel·or·ism

[MIM*145400]
increased width between the eyes due to an arrest in development of the greater wings of the sphenoid, thus fixing the orbits in the widely separated fetal position; autosomal dominant inheritance. Ocular hypertelorism is a feature of many syndromes. A distinct form [MIM*145410] shows other congenital defects such as hypospadias and esophageal anomalies.
See also: faciodigitogenital dysplasia.

Greig syndrome

(1) Ocular hypertelorism, see there.
(2) Greig polysyndactyly-craniofacial dysmorphism syndrome (MIM:175700).

oc·u·lar hy·per·tel·or·ism

(ok'yū-lăr hī'pĕr-tel'ŏr-izm)
Increased width between the eyes due to an enlarged sphenoid bone; other congenital anomalies and mental retardation may be associated.
Synonym(s): Greig syndrome, Opitz BBB syndrome, Opitz G syndrome.

Greig,

David M., Scottish physician, 1864-1936.
Greig syndrome - increased width between the eyes due to an enlarged sphenoid bone. Synonym(s): ocular hypertelorism

oc·u·lar hy·per·tel·or·ism

(ok'yū-lăr hī'pĕr-tel'ŏr-izm) [MIM*145400]
Increased width between the eyes due to an enlarged sphenoid bone; other congenital anomalies and mental retardation may be associated.
Synonym(s): Greig syndrome, Opitz BBB syndrome, Opitz G syndrome.
References in periodicals archive ?
Phenotype of five patients with Greig syndrome and microdeletion of 7p13.