Down syndrome is a genetic condition caused when an unusual cell division results in an extra full or partial copy of chromosome 21. This extra genetic material causes the developmental changes and physical features of Down syndrome. The term "syndrome" refers to a set of symptoms that tend to happen together. With a syndrome, there is a pattern of differences or problems. The condition is ...
Prader-Willi Syndrome Comprehensive Clinic Overview Prader-Willi syndrome is a genetic condition associated with cognitive and behavioral symptoms, delays in development, chronic hunger, and low levels of growth hormone. Babies with Prader-Willi syndrome may appear "floppy" and have difficulty with feeding, often requiring feeding tubes.
Diagnosis Bardet-Biedl syndrome is a very rare condition. Symptoms begin over time and may include many that can happen in other genetic conditions. Because of this, BBS may not be diagnosed right away. To diagnose BBS, your child's healthcare professional does a physical exam, checks weight and blood pressure, and talks with you about symptoms and your family history. Because many symptoms of ...
Am I correct in understanding that you haven't been diagnosed officially with hyoid bone syndrome, but upon your research you discovered that your symptoms match closely with HBS, correct? Now you are looking for a specialist who in knowledgeable about this syndrome. Have you considered consulting neurology and/or ENT at Mayo Clinic?
Kelly Wood, MD, is a board-certified endocrinologist with a special interest in osteoporosis and metabolic bone disease. Symptoms of Cushing's syndrome include a round face, weight gain, and muscle ...
In the early stages of serotonin syndrome, people may experience mild symptoms, such as tremors, dizziness, and headache. Serotonin syndrome, or serotonin toxicity, is a potentially serious drug ...