Peters anomaly
A rare, autosomal recessive inherited syndrome caused by mutations in the B3GALTL gene. It is characterized by abnormalities in the anterior chamber of the eye, short stature, cleft lip with or without cleft palate, distinctive facial features, and intellectual disability.
Disease Alternative Name
Recent Cases of Peters anomaly
Browse recently discussed Peters anomaly cases by specialistsTop Peters anomaly Doctors on Curofy
Top doctors who continously share their opinions on Peters anomalyAgartala Government Medical College & Govind Ballabh Pant Hospital
Ms Ophthalmology
Agartala Government Medical College & Govind Ballabh Pant Hospital
MS Ophthalmology
Navodaya Medical College Hospital & Research Centre
DO
Eye Care & Research Centre, Kolkata for About 25 Years
Consultant
Eye Care & Research Centre, Kolkata
MS, DO
Florence Hospital
Sr Consultant Ophthalmologist
POSTED MORE THAN 1600 OPHTHALMIC ARTICLES TILL DATE
Sarojini Devi Eye Hospital
MS
SDEH
MS
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