Indian Academy of Pediatrics (IAP) STANDARD TREATMENT GUIDELINES 2022 Thalassemia Lead Author Ajith Kumar VT Co-Authors Amita Mahajan, Joy Bhaduri Under the Auspices of the IAP Action Plan 2022 Remesh ...
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...Indian academy of pediatrics iap standard treatment guidelines thalassemia lead author ajith kumar vt co authors amita mahajan joy bhaduri under the auspices action plan remesh r president upendra kinjawadekar piyush gupta elect vineet saxena hsg committee chairperson coordinator national coordinators ss kamath vinod h ratageri member secretaries krishna mohan vishnu pt members santanu deb surender singh bisht prashant kariya narmada ashok pawan kalyan is an autosomal recessive disease it two main types i e alpha and beta mutation in hba genes four hbb gene one from such each parent severity signs involved synthesis symptoms directly proportional to number globin mutated with has no or children will have mild but a carrier can condition also called tion pass on minor people duc moderate severe this o trait major these tr babies are usually healthy at birth develop n within first years life three some manifest milder form intermedia result stillbirth death shortly after lifelong transfu...