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Samsonite (Guest)
Precautionary genetic baby testing can be done to screen out genetic disorders. Prenatal first and second trimester testing, amniocentesis or chorionic villus sampling clubbed with assessing nasal translucency on USG and newborn baby genetic testing by urine for 100 metabolic disorders are just to name few measures which one can take to diagnose genetic disorders.
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Replied on Thursday, December 30, 2010 5:43 AM
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Let me know is there any programme to reduce the birth rate of Thalassemia children ?
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Replied on Monday, June 6, 2011 9:15 PM
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I, Dr Shakila Shetty am working as a Senior prof of OBG at M.S.Ramaiah Medical Teaching Hospital, Bangalore. I would like to be a member of BDRI. Kindly tell me how to go about
Dr Shakila Shetty.
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Replied on Friday, December 25, 2015 10:51 AM
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