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Pallister W syndrome [Supplementary Concept]

A rare X-linked hereditary syndrome characterized by craniofacial abnormalities that include a prominent mandible, HYPERTELORISM, and distinct anterior cowlick, STRABISMUS; MUSCLE SPASTICITY; limited elbow motion, moderate to severe intellectual disability, and seizures. OMIM: 311450

Date introduced: August 25, 2010

MeSH Unique ID: C538106

Heading Mapped to:

Entry Terms:

  • W syndrome
  • Median cleft upper lip, mental retardation and pugilistic facies

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