Opitz syndrome
An autosomal dominant condition caused by mutation(s) in the ASXL1 gene, encoding putative polycomb group protein ASXL1. It is characterized by severe intrauterine growth retardation, profound mental retardation, craniofacial dysmorphisms, and flexion deformities of the upper limbs.
Disease Alternative Name
Recent Cases of Opitz syndrome
Browse recently discussed Opitz syndrome cases by specialists
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Top Opitz syndrome Doctors on Curofy
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Jagadguru Jayadeva Murugarajendra Medical College
Retired Professor and Head Pediatrics
Jagadguru Jayadeva Murugarajendra Medical College
md,frcpch(uk),ficpcc(London),masp(usa),phd, fams ,fimsa.
S M S Medical College & Hospital
Assistant Professor Ophthalmology
Dr R P Centre, AIIMS,
MD Ophthalmology
Niloufer Hospital
MD Pediatrics
Nilofer Hospital, Osmania Med College
MD pediatrics
Sepuri Endocrine & Diabetes Center
Chief Endocrinologist & Diabetologist for the Last 25 Years
Royal College of Physicians, United Kingdom
Masters Degree in Clinical Endocrinology & Diabetes
Rainbow Hospital
Registrar
Goa Medical College
MD Pediatrics
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