There is 8 Article with tag "Genetic Mutation"
Kallmann syndrome is a rare genetic disorder that occurs when the body does not produce enough gonadotropin-releasing hormone (GnRH).
Laurence-Moon-Bardet-Biedl Syndrome (SLMBB) is a rare genetic disorder that manifests through various health issues.
Metabolic disorders in infants affect how babies digest certain nutrients such as carbohydrates, fats, or proteins and convert these nutrients into fuel for their bodies.
McCune-Albright syndrome is a condition that affects the bones, skin, and various hormone-producing tissues.
Fanconi anemia (AF) is a rare inherited disorder that involves your bone marrow and many other parts of your body.
Smith-Lemli-Opitz syndrome (SLOS) is a genetic condition that attacks many parts of the body.
Lynch syndrome is a genetic condition that increases a person's risk of developing cancer
Cowden syndrome is a rare genetic disorder
