Emerging genetic therapies targeting Autosomal Recessive Congenital Ichthyoses (ARCI) present promising market opportunities due to unmet needs and rising prevalence. Improved diagnostics and ...

Autosomal dominant optic atrophy (ADOA), the most common genetic optic neuropathy, is an insidious disease. It often presents slowly during childhood by way of blurry vision, trouble reading or ...

Couples who were found to be genetic carriers for autosomal recessive or X-linked genetic conditions often opted to change their reproductive strategy, a large Australian population-based study found.

Rotor syndrome is a rare and typically harmless genetic condition affecting the liver. It causes jaundice, mild yellowing of skin and eyes, and generally doesn’t need treatment. Rotor syndrome is a ...

Please provide your email address to receive an email when new articles are posted on . Nephrectomy can be effectively performed in patients with autosomal dominant PKD for various indications, such ...

Researchers have conducted what they say is the largest and most diverse study to date on how recessive genetic changes contribute to developmental disorders. The team, headed by researchers at the ...

A new study examined the records of 4452 Asian patients with ADPKD treated at 2 tertiary-care centers over a period of 15 years. Patients with ADPKD had higher rates of post-transplant diabetes ...

Chromosomes are tightly coiled structures in each of your cells that contain DNA, the code for all life. DNA is organized in segments on chromosomes called genes. Humans typically have 46 chromosomes ...

Cystic fibrosis represents one of the most common inherited genetic disorders affecting people of European descent, touching the lives of approximately 30,000 individuals in the United States alone.