Doctors told Nate and Mandy Baldry that something wasn’t quite right with their daughter, Cora Baldry, a month before she was born when their baby was measuring small and the amniotic fluid ...
Carissah Holland, an Owasso girl with MPS VI, underwent multiple surgeries and advocates for others while pursuing her dreams ...
Three patients with spinal muscular atrophy had improved muscle strength and could walk farther after a month of daily spinal ...
Health and Me on MSN1d
What Is Alkaptonuria? The Rare Disease That Turns Your Pee Black – Here’s WhyAlkaptonuria is a rare genetic disorder that causes black urine due to homogentisic acid buildup, leading to joint pain, ...
3don MSN
Jay and Pamela both have Osteogenesis Imperfecta Type 3, a condition that causes fragile bones. Both get around in motorized ...
In two new papers, researchers from The Jackson Laboratory (JAX) report the successful use of two approaches -- gene therapy ...
Marcelo was diagnosed with Treacher Collins syndrome, a rare condition affecting facial bone structure and cartilage. The genetic disorder left Marcelo without ears and with a smaller-than-normal ...
A teenager was diagnosed with skin cancer and a brain tumour four times before she turned 18 after discovering she had a rare genetic disorder. Ruby-Jo Sneed discovered she had a rare genetic ...
In two new papers, researchers from The Jackson Laboratory (JAX) report the successful use of two approaches—gene therapy and ...
12h
Families of rare disease patients appeal to PM Modi and Health Minister for increased treatment funding support.
Emily Cooper says all bereaved families should be offered genetic testing if they lose a child to unexpected sudden death. | ...
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