X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome

Orpha code: 480907OMIM code: 300966

Definition

A rare multiple congenital anomalies/dysmorphic syndrome characterized by global developmental delay, intellectual disability, growth retardation, hearing impairment, characteristic facial dysmorphology (including prominent supraorbital ridges, downslanting palpebral fissures, deep-set eyes, long face, sagging cheeks, anteverted nares, and pointed chin), generalized hypotonia, joint hypermobility, gluteal crease with sacral caudal remnant and sacral dimple, and variable neurological features. Various ophthalmic, cutaneous, musculoskeletal, gastrointestinal, and cardiovascular anomalies have also been described.

Disease data
Classification

Malformation syndrome

ORPHA code
480907
OMIM code
300966
ICD10 code
-
ICD11 code
-

No additional description.

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