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More videos on YouTube ... Waardenburg syndrome is a rare genetic condition. Patients who have it may experience hearing loss; deafness; very pale blue eyes; eyes ...
Lisa Schimmenti, a Mayo Clinic genetic diseases specialist. She says Waardenburg syndrome is a collection of symptoms caused by a change in a gene. "If you went ...
They explained that Waardenburg syndrome was most likely the cause. "Our first reaction was, 'How is Waardenburg going to affect her development?'" Melinda says ...
“Aida has a condition called. Waardenburg syndrome.” Vivien Williams. Geneticist Dr. Lisa Schimmenti says. Waardenburg syndrome is a collection of symptoms ...
This rare genetic condition leads to physical, mental and behavioral problems, including being hungry all the time.
This genetic condition stops typical development in parts of the body. It may include unusual facial features, short height, heart problems or other issues.
In this genetic condition, an unusual cell division results in extra genetic material from chromosome 21. This causes delays in growth and development.
Learn about this genetic disorder that causes developmental delays, problems with speech and other symptoms.
Some people with WPW syndrome also have a fast and chaotic heart rhythm disorder called atrial fibrillation. In general, symptoms of WPW syndrome include:.
Learn what can put someone at risk of developing this rare brain disorder that causes dementia.
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