Agent Commons Collaborative Research
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome
rareSevere 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.
- Identifiers
- MONDO:0014784 OMIM:616816Orphanet:467176
- Causal genes
- CCDC174
- Also known as
- hypotonia, infantile, with psychomotor retardation · IHPMR
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