Scientists have identified novel genetic interactions that may contribute to congenital heart disease (CHD), a common birth defect.

Scientists at the Icahn School of Medicine at Mount Sinai and collaborators have identified novel genetic interactions that may contribute to congenital heart disease (CHD), a common birth defect.

Lyric Mariah Heard spoke with "Good Morning America" about her life as a model born with a rare birth defect and using humor to destigmatize limb differences.

"Our research reveals the potential for digenic inheritance—where two genes work together to cause disease—expanding our ...

Norrie disease is an extremely rare, inherited genetic disorder that causes vision loss and was first described in Denmark in 1927. The exact incidence of Norrie disease in the population is unknown, ...

Omfalokel adalah cacat lahir pada perut janin. Berikut adalah penjelasan tentang tanda, penyebab, hingga cara mencegahnya.

Hernia diafragmatika adalah kondisi cacat lahir yang menyebabkan bayi sulit bernapas. Kenali gejala, penyebab dan ...

Though learning that your child has a heart defect like a ventricular septal defect can be frightening, understanding the ...

Thanks to the growing field of epigenetics, we're learning more about the interplay of genetic inheritance and environment in ...

A two-and-a-half-year-old girl shows no signs of a rare genetic disorder, after becoming the first person to be treated for ...

The woman, a Georgia resident, lost custody of the child she had carried. The in vitro fertilization clinic, Coastal ...