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Syndromic orbital border hypoplasia

Orpha number ORPHA98606
Synonym(s) Urrets-Zavalia syndrome
Prevalence -
Inheritance -
Age of onset -
ICD-10 -
OMIM
UMLS -
MeSH -
MedDRA -
SNOMED CT -

Summary

Syndromic orbital border hypoplasia is a rare disorder observed in two families to date and characterized by agenesis of the orbital margin, varying defects of the lacrimal passages, hypoplasia of the palpebral skin and tarsal plates and atresia of the nasolacrimal duct.


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