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3M syndrome
Genetics:
1) autosomal recessive disorder
2) associated with defects in the CUL7 gene
Clinical manifestations:
1) severe pre- & postnatal growth retardation
2) facial dysmorphism
3) large head circumference
4) normal intelligence & endocrine function
5) skeletal changes include long slender tubular bones & tall vertebral bodies.
Related
Cullin-7; CUL-7 (CUL7, KIAA0076)
General
genetic syndrome (multisystem disorder)
Database Correlations
OMIM 273750
References
OMIM :accession 273750