Anophthalmia plus syndrome

Orpha code: 1104OMIM code: 600776

Definition

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.

Disease data
Classification

Malformation syndrome

Synonyms
Fryns microphthalmia syndrome
Mikroftalmia z rozszczepem twarzy
Zespół mikroftalmii Frynsa
Microphthalmia with facial clefting
ORPHA code
1104
OMIM code
600776
ICD10 code
Q87.8
ICD11 code
LD21.0

No additional description.

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