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Waardenburg Syndrome is often referred to as Waardenburg Shah Syndrome or Waardenburg-Klein syndrome. It is one of the rare genetic disorders which is defined by different levels of deafness. There are high chances that the problem is present from birth and would include symptoms like minor defects in structures arising from the neural crest. Babies with this disease would 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?
There is no specific treatment. Symptoms will be treated as needed. Special diets and medicines to keep the bowel moving are prescribed to those people who have constipation. Hearing should be checked closely.
DID YOU KNOW?
Along with human beings, this is a problem that is also known to affect ferrets.