World Of Taxonomy
C124839Level 5

Pettigrew Syndrome

**Semantic type:** Disease or Syndrome

**Definition:** A rare, X-linked inherited syndrome characterized by mental retardation and additional features, which include choreoathetosis, hydrocephalus, Dandy-Walker malformation, seizures, and iron or calcium deposition in the brain.

**Synonyms:** - PGS

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C124839 - Pettigrew Syndrome - NCI Thesaurus - World Of Taxonomy | World Of Taxonomy