GENETIC DISORDER
There is 22 Article with tag "Genetic Disorder"
Rubinstein-Taybi Syndrome
Rubinstein-Taybi syndrome is characterized by short stature, intellectual disability, distinctive facial features, and broad thumbs and toes.
Kallmann's Syndrome
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
Laurence-Moon-Bardet-Biedl Syndrome (SLMBB) is a rare genetic disorder that manifests through various health issues.
Patau Syndrome (Trisomy 13)
Patau syndrome (trisomy 13) is a chromosomal disorder caused by the presence of an extra chromosome 13.
Metabolic Disorders in Infants
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
McCune-Albright syndrome is a condition that affects the bones, skin, and various hormone-producing tissues.
Facioscapulohumeral Muscular Dystrophy (FSHD)
Facioscapulohumeral muscular dystrophy (FSHD) is a genetic disorder of the muscles of the face, shoulders, and upper arms.
Understanding the Effects of Congenital Adrenal Hyperplasia on Female Health
Certain medical conditions can cause women to exhibit physical characteristics typically associated with men.
Neurofibromatosis
Understand the causes, risk factors, symptoms, prevention, and treatment of Neurofibromatosis. Tumors in nerve cells.
Lipodystrophy
Lipodystrophy is an abnormal condition characterized by the loss of all or part of the tissue (fat) in your body.
Hemochromatosis
Hemochromatosis is a condition that causes your body to absorb too much iron from the foods you eat.