Search Results 1-10 of 16676 for waardenburg syndrome
Experts at Mayo Clinic diagnosed Aida with a condition called Waardenburg syndrome, a rare genetic disorder that causes deafness and pigment changes of the hair ...
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 causes weight gain, extra fingers or toes, kidney conditions, vision loss, and changes in development.
This complication of an unrepaired congenital heart defect needs to be watched closely. Learn how treatment can help manage symptoms.
This rare genetic condition leads to physical, mental and behavioral problems, including being hungry all the time.
This inherited disease causes copper to build up in vital organs, especially the liver, brain and eyes. It's treatable when caught early.
This genetic condition stops typical development in parts of the body. It may include unusual facial features, short height, heart problems or other issues.
Typically, signs and symptoms of Horner syndrome include decreased pupil size, a drooping eyelid and decreased sweating on the affected side of the face.
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