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Peters-plus syndrome
Genetics:
1) autosomal recessive disorder
2) associated with defects in B3GALTL gene
Clinical manifestations:
1) anterior eye-chamber abnormalities
2) disproportionate short stature
3) developmental delay
4) characteristic craniofacial features
- cleft lip &/or palate
General
genetic syndrome (multisystem disorder)
developmental disorder
Database Correlations
OMIM 261540
References
OMIM :accession 261540