Search Results 1-10 of 16533 for waardenburg syndrome
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 ...
She says Waardenburg syndrome is a collection of symptoms caused by a change in a gene. "If you went and Googled this disorder, you'll see pictures of ...
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.
Learn about this genetic disorder that causes developmental delays, problems with speech and other symptoms.
In this genetic condition, an unusual cell division results in extra genetic material from chromosome 21. This causes delays in growth and development.
Some people with WPW syndrome also have a fast and chaotic heart rhythm disorder called atrial fibrillation. In general, symptoms of WPW syndrome include:.
This rare disease causes an early decay of nerve cells in the brain. Learn about its symptoms and how treatments may help.
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