The NHS has announced that newborns will be screened for a rare, life-threatening metabolic disorder that can lead to kidney ...

A 58-year-old Thane resident donates part of his liver to save granddaughter Divisha from biliary atresia, restoring her ...

If a toothpick had pierced the man's duodenum, it would completely explain all of the man's symptoms. He drank too much and ...

NHS England will now screen newborns for a rare genetic condition that can lead to serious liver, kidney, and neurological ...

After two children passed from a rare genetic disease, New Orleans mom Missy Ward wrote a memoir from the perspective of her ...

Hereditary Tyrosinaemia Type 1 (HT1) is a rare, genetically inherited disorder that affects around 7 babies per year in the UK. Left untreated, it can lead to severe complications such as organ damage ...

Following Varinder Singh Ghuman’s sudden death, hepatologist Dr Cyriac Abby Philips explains how intense bodybuilding and ...

The test for HT1 has been added to the NHS Newborn Blood Spot Screening Programme following a recommendation by the UK ...

Newborn babies in England will be routinely screened for a rare genetic condition that can cause long-term health problems if ...

Once screened by the NHS, babies with HT1 can be given medication called Nitisinone, which helps to prevent high levels of ...

Newborn babies will be routinely screened for a rare genetic condition, the NHS England has announced. Hereditary ...