skip banner - Return to original view
site viewing options
 
Parents|Medical Information|Professionals|In your area|Get involved|Campaigns
Print page

Directory Cover image Subscribe to the Contact a Family Directory

 

This website is certified by Health On the Net Foundation. Click to verify. This site complies with the HONcode standard for trustworthy health information: verify here.

Williams syndrome

Background

Williams syndrome: Infantile Hypercalcaemia; Williams-Beuren syndrome

Williams syndrome is a rare congenital (present at birth) condition that is caused by missing genetic material from chromosome 7. Individuals with Williams syndrome are affected to differing degrees and display typical facial features as well as developmental delay.

What are the symptoms? View What are the symptoms?

Medical text written July 2011 by Dr K Metcalf, Consultant Clinical Geneticist, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.

 

Tell us what you think of this information...

Print whole article Print whole article

 


This Web Site © Copyright, Contact a Family 2011
Contact a Family, 209-211 City Road, London EC1V 1JN
Tel: 020 7608 8700

Registered Charity No. 284912. Charity registered in Scotland No. SC039169
Company limited by guarantee, registered in England and Wales No. 1633333.
HM Revenue & Customs charity tax reference No. XN54769. VAT Reg. No. GB 749 3846 82

Contact a Family Twitter Contact a Family Facebook Contact a Family iTunes Contact a Family YouTube