Severe myopia-generalized joint laxity-short stature syndrome

Orpha code: 527450OMIM code: 617662

Definicja

A rare developmental defect with connective tissue involvement characterized by joint hyperextensibility and multiple dislocations of large joints, severe myopia, and short stature. Other common features include retinal detachment, iris and chorioretinal coloboma, kyphoscoliosis and other spine deformities, pectus carinatum, talipes equinovarus, and progressive hearing loss.

Disease data
Klasyfikacja

Malformation syndrome

Kod ORPHA
527450
Kod OMIM
617662
Kod ICD10
-
Kod ICD11
-

No additional description.

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