Waardenburg-Shah Syndrome treatment in Celaya

Waardenburg-Shah syndrome is a rare variant of Waardenburg syndrome that brings together particularities in pigmentation and hearing with a bowel disorder that hinders its normal movement.

How it presents: It may include changes in the color of the hair, skin or eyes, hearing loss and digestive problems due to involvement of the final part of the intestine.

Common causes: It stems from a genetic disorder that influences the development of certain cells during the formation of the embryo.

Which specialist treats it? The pediatrician performs the newborn's initial evaluation and coordinates with genetics, gastroenterology and pediatric audiology depending on each case. When combined signs of pigmentation, hearing or bowel transit appear in a baby, it is advisable to consult a professional soon.