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Cystic fibrosis (CF) is a genetic disorder that affects multiple organs in the body, primarily the lungs and pancreas. People with CF inherit a…
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a condition that causes numerous fluid-filled sacs, called cysts, to grow in your kidneys.…
Mucopolysaccharidosis Type I, or MPS I, is a rare genetic disorder that affects children. It is caused by a deficiency in an enzyme called alpha-L…
Pfeiffer syndrome is a rare genetic disorder that affects the development of a baby's skull and face. This condition causes the skull bones to fuse…
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Get a free consultationInfantile spasms, also known as West syndrome, is a rare type of seizure disorder that affects babies. If your baby has been diagnosed with infantile…
Trisomy 13, also known as Patau syndrome, is a rare genetic condition that occurs when a baby has an extra 13th chromosome. This extra genetic…
Rapp-Hodgkin syndrome is a rare genetic disorder that affects various parts of the body, including hair, nails, skin, sweat glands, and teeth. It is…
Klinefelter syndrome is a genetic condition that affects males who are born with an extra X chromosome. Instead of the typical XY chromosome pattern,…
If you or your child has been diagnosed with a germ cell tumor, it's essential to understand what this means and what steps to take next. Germ cell…
Sickle cell disease (SCD) is a genetic disorder that affects the shape and flexibility of red blood cells. When these cells become hard and curved,…
Hereditary angioedema (HAE) is a rare genetic condition that causes swelling under the skin and lining of the gut and lungs. If you or a loved one…
Diamond-Blackfan Anemia (DBA) is a rare blood disorder that affects the body's ability to produce red blood cells. Red blood cells are essential for…
About 15% of women with breast cancer have a family history of the disease. Having a close relative, such as a mother, sister, or daughter, with…
