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Anophthalmia plus syndrome
rareAnophthalmia 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.
- Identifiers
- MONDO:0010930 OMIM:600776Orphanet:1104
- Part of
- Multiple congenital anomalies/dysmorphic syndrome without intellectual disabilitySyndromic disease
- 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
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