Intellectual disability, Wolff type

Intellectual disability, Wolff type is a rare intellectual disability syndrome characterized by severe intellectual disability, characteristic facial features (low anterior hairline, upward slanting palpebral fissures, ocular hypertelorism, broad, bulbous nose, large ears with helix incompletely developed, thick lips, and micrognathia) and additional anomalies including peripheral joint contractures, delayed skeletal maturation, bilateral cleft lip and palate, strabismus, terminal hypoplasia of fingers, hypospadias, and bilateral inguinal hernias.

Also known as: Wolff-Zimmermann syndrome, WOLFF intellectual disability syndrome, WOLFF mental retardation syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, Wolff type itself.