Coffin-Lowry syndrome

Orpha code: 192OMIM code: 303600

Definicja

A rare X-linked syndromic intellectual disability characterized by global development delay, postnatal growth retardation leading to short stature, facial dysmorphism, short hands with tapering fingers and progressive skeletal abnormalities including kyphoscoliosis and <i>pectus carinatum/excavatum</i>. Intellectual disability ranges from mild to severe.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
CLS
CLS
Kod ORPHA
192
Kod OMIM
303600
Kod ICD10
Q87.0
Kod ICD11
LD2F.1Y

No additional description.

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