MeSH Browser

MeSH Supplementary: Pallister W syndrome
Unique ID: C538106
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538106
Entry Term(s): Median cleft upper lip, mental retardation and pugilistic facies; W syndrome
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; *Intellectual Disability; *Craniofacial Abnormalities
Frequency: 11
Note: 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 of Entry: 2010/08/25
Revision Date: 2016/09/29

Pallister W syndrome MeSH Supplementary Concept Data 2025