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).

Also known as: camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye, Rozin hertz Goodman syndrome, camptodactyly, joint contractures, facial skeletal defects

0 clinical trials for this condition and its sub-types, 0 tagged with Camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye itself.