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The term Waardenburg Syndrome is also called Waardenburg Shah Syndrome or Waardenburg-Klein syndrome, which is defined as a rare genetic disorder most often characterized by different levels of deafness. In many cases, the problem is present from birth and would include symptoms like minor defects in structures arising from the neural crest. Such individuals would also have pale skin and blue eyes of different colors and they are prone to hearing loss and issues.
HOW IS WAARDENBURG SYNDROME DIAGNOSED?
Diagnosis of Waardenburg Syndrome is based on specific symptoms and clinical evaluation. The ear-nose-throat specialist may conduct an audiometry test to check for deafness. Bowel transit time, colon biopsy and genetic testing are other diagnostic tests for confirming Waardenburg Syndrome
HOW IS WAARDENBURG SYNDROME TREATED?
The treatment procedure for Waardenburg Syndrome is not really available as it is an irreversible health problem. However, people who suffer from the same should consult a genetic expert as there is a high chance of this disorder being passed on to the offspring.
DID YOU KNOW?
Along with human beings, this is a problem that is also known to affect ferrets.