21 Sept 2018
Newborn screening has not been a priority among Indian parents, but if it is done, it can help detect diseases which the child may be susceptible to later in life, said doctors. It is stated that every 64th newborn inherits a genetic disease from the family. An early diagnostic test (via blood or urine) performed within 72 hours of a child's birth, can help identify the causes and detect the possible higher risk of developing disorders among infants such as permanent neurological disorders and physical damage, Trivitron Healthcare Chairman and MD Dr GSK Velu said on Thursday. It is stated that every 64th newborn inherits a genetic disease from the family. An early diagnostic test (via blood or urine) performed within 72 hours of a child's birth, can help identify the causes and detect the possible higher risk of developing disorders among infants such as permanent neurological disorders and physical damage, Trivitron Healthcare Chairman and MD Dr GSK Velu said on Thursday. It is stated that every 64th newborn inherits a genetic disease from the family. An early diagnostic test (via blood or urine) performed within 72 hours of a child's birth, can help identify the causes and detect the possible higher risk of developing disorders among infants such as permanent neurological disorders and physical damage, Trivitron Healthcare Chairman and MD Dr GSK Velu said on Thursday. September is considered Newborn Screening Month. He said that there is a need to create awareness about newborn screening and the best way is through government programmes and the only way to achieve it is by making newborn screening a constitutional mandate, for a safer and healthier tomorrow. September is considered Newborn Screening Month. He said that there is a need to create awareness about newborn screening and the best way is through government programmes and the only way to achieve it is by making newborn screening a constitutional mandate, for a safer and healthier tomorrow. Newborn screening is a preventive step to reduce infant mortality. This is done by idenÂtiÂfyÂing genetic disÂorÂders that are inÂherÂited and also those which are caused by the enÂviÂronÂment,†said Dr Vinod Jain, seÂnior facÂulty KGMU and a pubÂlic health exÂpert. “NewÂborn screenÂing is a preÂvenÂtive step to reÂduce inÂfant morÂtalÂity. This is done by idenÂtiÂfyÂing genetic disÂorÂders that are inÂherÂited and also those which are caused by the enÂviÂronÂment,†said Dr Vinod Jain, seÂnior facÂulty KGMU and a pubÂlic health exÂpert. InÂfants can be saved from health comÂpliÂcaÂtions such as menÂtal reÂtarÂdaÂtion, seÂvere aneÂmia and lacÂtose intolerance with the help of timely idenÂtiÂfiÂcaÂtion and medÂiÂcal inÂterÂvenÂtion. NewÂborn screenÂing has not been a priÂorÂity among InÂdian parÂents, but if it is done, it can help deÂtect disÂeases which the child may be susÂcepÂtiÂble to later in life, said docÂtors. “It is stated that evÂery 64th newÂborn inÂherÂits a genetic disease from the famÂily. An early diÂagÂnosÂtic test (via blood or urine) perÂformed within 72 hours of a child’s birth, can help idenÂtify the causes and deÂtect the posÂsiÂble higher risk of deÂvelÂopÂing disÂorÂders among inÂfants such as perÂmaÂnent neuÂroÂlogÂiÂcal disÂorÂders and physÂiÂcal daÂmÂage,†TrivÂitÂron HealthÂcare ChairÂman and MD Dr GSK Velu said on ThursÂday. “It is stated that evÂery 64th newÂborn inÂherÂits a genetic disease from the famÂily. An early diÂagÂnosÂtic test (via blood or urine) perÂformed within 72 hours of a child’s birth, can help idenÂtify the causes and deÂtect the posÂsiÂble higher risk of deÂvelÂopÂing disÂorÂders among inÂfants such as perÂmaÂnent neuÂroÂlogÂiÂcal disÂorÂders and physÂiÂcal daÂmÂage,†TrivÂitÂron HealthÂcare ChairÂman and MD Dr GSK Velu said on ThursÂday. “It is stated that evÂery 64th newÂborn inÂherÂits a genetic disease from the famÂily. An early diÂagÂnosÂtic test (via blood or urine) perÂformed within 72 hours of a child’s birth, can help idenÂtify the causes and deÂtect the posÂsiÂble higher risk of deÂvelÂopÂing disÂorÂders among inÂfants such as perÂmaÂnent neuÂroÂlogÂiÂcal disÂorÂders and physÂiÂcal daÂmÂage,†TrivÂitÂron HealthÂcare ChairÂman and MD Dr GSK Velu said on ThursÂday. SeptemÂber is conÂsidÂered NewÂborn ScreenÂing Month. He said that there is a need to creÂate awareÂness about newÂborn screenÂing and the best way is through govÂernÂment programmes and the only way to achieve it is by makÂing newÂborn screenÂing a conÂstiÂtuÂtional manÂdate, for a safer and healthÂier toÂmorÂrow. SeptemÂber is conÂsidÂered NewÂborn ScreenÂing Month. He said that there is a need to creÂate awareÂness about newÂborn screenÂing and the best way is through govÂernÂment programmes and the only way to achieve it is by makÂing newÂborn screenÂing a conÂstiÂtuÂtional manÂdate, for a safer and healthÂier toÂmorÂrow. “NewÂborn screenÂing is a preÂvenÂtive step to reÂduce inÂfant morÂtalÂity. This is done by idenÂtiÂfyÂing genetic disÂorÂders that are inÂherÂited and also those which are caused by the enÂviÂronÂment,†said Dr Vinod Jain, seÂnior facÂulty KGMU and a pubÂlic health exÂpert. “NewÂborn screenÂing is a preÂvenÂtive step to reÂduce inÂfant morÂtalÂity. This is done by idenÂtiÂfyÂing genetic disÂorÂders that are inÂherÂited and also those which are caused by the enÂviÂronÂment,†said Dr Vinod Jain, seÂnior facÂulty KGMU and a pubÂlic health exÂpert. InÂfants can be saved from health comÂpliÂcaÂtions such as menÂtal reÂtarÂdaÂtion, seÂvere aneÂmia and lacÂtose intolerance with the help of timely idenÂtiÂfiÂcaÂtion and medÂiÂcal inÂterÂvenÂtion.
