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Article

Coffin-Lowry syndrome: clinical and molecular features.

Journal of medical genetics - 1 Oct 2002

Hanauer A, Young I D

Abstract excerpt

The Coffin-Lowry syndrome (CLS) is a rare X linked disorder in which affected males show severe mental retardation with characteristic dysmorphism, most notably affecting the face and hands. The typical facial features consist of a prominent forehead, hypertelorism, a flat nasal bridge, downward sloping palpebral fissures, and a wide mouth with full lips. Mild progression in facial coarsening occurs during...

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Source

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Identifiers

PMID: 12362025
DOI: 10.1136/jmg.39.10.705
PMCID: PMC1734994

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Coffin-Lowry syndrome: clinical and molecular features.PMID 12362025Read ↗

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