Congenital limbs-face contractures-hypotonia-developmental delay syndrome

Orpha code: 562528OMIM code: 616266

Definicja

A rare multiple congenital anomalies/dysmorphic syndrome with intellectual disability characterized by severe congenital contractures of the limbs and face, hypotonia, neonatal respiratory distress, and global developmental delay. Dysmorphic facial features include downslanting palpebral fissures, broad nasal bridge, large nares, long philtrum, and deep nasolabial folds, among others. Limb deformities (camptodactyly, clubfoot), short neck, scoliosis, as well as seizures have also been reported. Brain MRI may show cerebral and cerebellar atrophy in some cases.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
CLIFAHDD syndrome
Zespół CLIFAHDD
Kod ORPHA
562528
Kod OMIM
616266
Kod ICD10
Q87.8
Kod ICD11
-

No additional description.

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