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What is Wilson disease?

Wilson disease is a genetic disorder in which copper does not get excreted from the body. This excess copper builds up in the liver, brain, eyes, and other organs. If left untreated, Wilson disease can cause severe brain damage and neurological symptoms, liver failure, and death.

What are the symptoms of Wilson disease?

The presentation may occur from 3 to 55 years of age. It is suspected when a young patient presents with acute liver failure or cirrhosis.
Symptoms of Wilson disease depend on the predominantly affected organ and include:
  • recurrent jaundice,
  • abdominal distension (fluid in the abdomen)
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FAQs_Wilsonmeeting_Dec2012.pdf418.14 KB

Conference Secreteriat

Nagral Clinic, O-18, Nav Bhavna,
Veer Savarkar Marg, Prabhadevi, Mumbai-400025

E-mail pedliver@gmail.com

Contact Persons:
Priya- 9224791366
Samrudhi-9146652684

  • To promote research into paediatric liver disease
  • To spread awareness about paediatric liver disease amongst medical professionals and the public through lectures, educational material, website, conferences, workshops (national and international)  and other media and activities. This includes post diagnostic measures as well as supporting & creating awareness  of preventive measures as may be possible , including vaccination etc.... 

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