Symptomatic form of Coffin-Lowry syndrome in female carriers

Orpha code: 276630OMIM code:

Definition

A rare X-linked syndromic intellectual disability which in symptomatic, female carriers is characterized by a highly variable phenotype including facial dysmorphisms (prominent forehead, hypertelorism, down-slanting palpebral fissures, epicanthic folds, thick lips with everted lower vermilion, thick nasal alae, and septum), short hands with tapering fingers, short stature and skeletal findings (progressive kyphoscoliosis). Intellectual disability is mild to moderate, but intellect can also be normal. A high rate of psychiatric disorders has also been reported.

Disease data
Classification

Malformation syndrome

ORPHA code
276630
OMIM code
-
ICD10 code
Q87.0
ICD11 code
-

No additional description.

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