Rajiv Gandhi University of Health Sciences, Karnataka
Fellowship Examination — 08-Sep-2023
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[Time: 3 Hours] [Max. Marks: 100]
PAEDIATRIC GENETICS - PAPER-I
QP Code: 4142
Your answers should be specific to the questions asked.
Draw neat labeled diagrams wherever necessary.
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Answer All The Questions 10 X 10 = 100 Marks
- Clinical features, genetics and recent advances in the management of Prader Willi syndrome.
- Discuss genetic testing in a child with Achondroplasia and write a brief note on the newer advances in the treatment of Achondroplasia.
- Ethical issues in prenatal diagnosis.
- Clinical features and genetic counselling in Edward syndrome.
- Amniotic band sequence.
- Approach to a child with congenital bilateral profound hearing loss.
- Substrate reduction therapy (SRT).
- Role of Hematopoietic stem cell transplantation in genetic disorders.
- Clinical feature and genetics of ataxia telangiectasia.
- Genetics and management of osteogenesis imperfecta.
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This download link is referred from the post: RGUHS Post Graduate Fellowship Examination Last 10 Years 2015-2025 Previous Question Papers || Rajiv Gandhi University of Health Sciences
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