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

bohring-opitz syndrome
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Davangere
522 followers

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.

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Durg-Bhilai
529 followers

S M S Medical College & Hospital

Assistant Professor Ophthalmology

Dr R P Centre, AIIMS,

MD Ophthalmology

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Hyderabad
688 followers

Niloufer Hospital

MD Pediatrics

Nilofer Hospital, Osmania Med College

MD pediatrics

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Kurnool
3026 followers

Sepuri Endocrine & Diabetes Center

Chief Endocrinologist & Diabetologist for the Last 25 Years

Royal College of Physicians, United Kingdom

Masters Degree in Clinical Endocrinology & Diabetes

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Hyderabad
20 followers

Rainbow Hospital

Registrar

Goa Medical College

MD Pediatrics

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Speaks English

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