Agent Commons Collaborative Research

Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome

rare

Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome is a rare, genetic, non-dystrophic congenital myopathy disorder characterized by a neonatal-onset of severe generalized hypotonia associated with mild psychomotor delay, congenital strabismus with abducens nerve palsy, and atrial and/or ventricular septal defects. Cryptorchidism is commonly reported in male patients and muscle biopsy typically reveals increased variability in muscle fiber size.

Causal genes
CCDC174
Also known as
hypotonia, infantile, with psychomotor retardation · IHPMR

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