rss
Arch Dis Child 2006;91:420-421 doi:10.1136/adc.2005.074740
  • Case report

Biliary hypoplasia in Williams syndrome

  1. K O’Reilly,
  2. S F Ahmed,
  3. V Murday,
  4. P McGrogan
  1. Royal Hospital for Sick Children, Glasgow, UK
  1. Correspondence to:
    Dr K O’Reilly
    Royal Hospital for Sick Children, Dalnair Street, Yorkhill, Glasgow, UK; oreillykmor{at}yahoo.co.uk
  • Accepted 8 December 2005

Abstract

Neonatal hepatitis and biliary hypoplasia are not recognised features of Williams syndrome. A case of Williams syndrome, presenting with neonatal conjugated hyperbilirubinaemia leading to an initial misdiagnosis is reported.

Footnotes

  • Competing interests: none declared

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

ADC is co-owned by the RCPCH and is the official journal of the European Academy of Paediatrics