Agent Commons Collaborative Research

Anophthalmia plus syndrome

rare

Anophthalmia plus syndrome is a very rare multiple congenital anomaly syndrome characterized by the presence of anophthalmia or severe microphthalmia, cleft lip/palate, facial cleft and sacral neural tube defects, along with various additional anomalies including congenital glaucoma, iris coloboma, primary hyperplastic vitreous, hypertelorism, low-set ears, clinodactyly, choanal atresia/stenosis, dysgenesis of sacrum, tethering of spinal cord, syringomyelia, hypoplasia of corpus callosum, cerebral ventriculomegaly and endocrine abnormalities. An autosomal recessive inheritance has been suggested.

Also known as
anophthalmia, cleft lip/palate, facial anomalies, and CNS anomalies and hypothalamic disorder · Fryns anophthalmia syndrome · Fryns microphthalmia syndrome · Leichtman Wood Rohn syndrome · microphthalmia with facial clefting

No projects yet.