This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Go to /pro/cpd-dashboard page

This page is worth 0.05 CPD credits. CPD dashboard

Go to /account/subscription-details page

This page is worth 0.05 CPD credits. Upgrade to Pro

Galactosaemia

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Galactosaemia is an autosomal recessive condition caused by the absence of galactose-1-phosphate uridyl transferase, which results in intracellular accumulation of galactose-1-phosphate which is highly toxic. It has an incidence of 1/60,000 in the UK.

Affected infants are normal at birth but upon commencement of milk feeds the majority suffer:

  • jaundice
  • vomiting
  • diarrhoea
  • failure to thrive

Related pages

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.