Peters-plus syndrome

Genetics

• autosomal recessive disorder
• associated with defects in B3GALTL gene

Clinical manifestations

• anterior eye-chamber abnormalities
• disproportionate short stature
• developmental delay
• characteristic craniofacial features
  • cleft lip &/or palate

More general terms

• genetic syndrome (multisystem disorder)
• developmental disorder

Database

• OMIM: https://mirror.omim.org/entry/261540