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Up to: Hereditary disease · Syndromic disease · Multiple congenital anomalies/dysmorphic syndrome without intellectual disability · Dysostosis
Camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye
A rare multiple congenital anomalies syndrome characterized by the association of camptodactyly, multiple eye defects (fibrosis of the medial rectus muscle, severe myopia, ptosis and exophthalmos), scoliosis, flexion contractures and facial anomalies (arched eyebrows, facial asymmetry with an abnormal skull shape, a prominent nose, small mouth, low-set and dysplastic ears, and a low nuchal hairline).
This condition has no sub-types.