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Pediatric Dubin-Johnson Syndrome
Dubin-Johnson syndrome causes jaundice, which is a yellow tint to the skin and whites of the eyes.
What is Pediatric Dubin-Johnson Syndrome?
Dubin-Johnson syndrome is when someone older than a newborn develops jaundice (a yellow caste of the skin and whites of the eyes). Jaundice is a fairly common condition that affects otherwise healthy newborn babies. However, Dubin-Johnson syndrome usually appears in adolescence (12-17 years of age*) or early adulthood.
Dubin-Johnson syndrome seems to most frequently affect Jewish Iranian and Moroccan people living in Israel, as well as Japanese people. However, it can affect people of any ethnic background.
What are the signs and symptoms of Pediatric Dubin-Johnson Syndrome?
- Jaundice
- Muscle weakness
- Nausea and/or vomiting
- Pain in the upper abdomen
*Age of adolescence as defined by the Centers for Disease Control (CDC).
What are the causes of Pediatric Dubin-Johnson Syndrome?
A gene mutation that is hereditary (passed down in families) causes Dubin-Johnson syndrome.
Pediatric Dubin-Johnson Syndrome Doctors and Providers
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Amal Aqul, MD Pediatric Hepatologist -
Lauren Lazar, MD Pediatric Gastroenterologist -
Megha Mehta, MD Pediatric Gastroenterologist -
Charina Ramirez, MD Pediatric Gastroenterologist -
Norberto Rodriguez-Baez, MD Pediatric Hepatologist -
Isabel Rojas Santamaria, MD Pediatric Gastroenterologist -
Phuong Luu, PA-C Physician Assistant - Gastroenterology -
Jennifer Peacock, APRN, PNP-PC Nurse Practitioner - Gastroenterology