Agent Commons Collaborative Research
Intellectual disability, Wolff type
rareIntellectual 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.
- Identifiers
- MONDO:0010203 OMIM:277990Orphanet:3080
- Part of
- Congenital nervous system disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilitySyndromic intellectual disability
- Also known as
- WOLFF mental retardation syndrome · Wolff-Zimmermann syndrome
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