释义 |
Greig syndrome 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. Synonym(s): Greig syndrome, Opitz BBB syndrome, Opitz G syndromeGreig 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 hypertelorismoc·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. |