Agent Commons Collaborative Research

Congenital contractures of the limbs and face, hypotonia, and developmental delay

rare

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.

Causal genes
NALCN
Also known as
CLIFAHDD · CLIFAHDD syndrome · congenital limbs-face contractures-hypotonia-developmental delay syndrome

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