Cure My Disease

Don't miss your cure!

Home News Browse About
Log in / Sign up

Galactokinase deficiency

MONDO:0009255

Galactokinase deficiency is a rare mild form of galactosemia characterized by early onset of cataract and an absence of the usual signs of classic galactosemia, i.e. feeding difficulties, poor weight gain and growth, lethargy, and jaundice.

Also known as: GALK deficiency, GALK-D, galactokinase deficiency, galactokinase deficiency galactosemia, galactokinase deficiency with cataracts, galactosemia type 2, Galk deficiency, galactosemia 2

34 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Eye disorder (97) Inborn errors of metabolism (42) Human disease (14) Galactosemia (5) Carbohydrate metabolism disease (3) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2)
Trials to join now! 20 Not yet recruiting 3 Not yet finished but already full! 5 Completed 5 Terminated 1
Sort by
  • VR headsets tested as a possible treatment for blindness

    Disease control Terminated

    This study tested whether using a virtual reality headset for one-hour sessions could help regenerate damaged optic nerves and improve vision in people with glaucoma or other retinal diseases. The idea came from promising results in rodents. However, the trial was terminated earl…

    Phase: NA • Sponsor: Stanford University • Aim: Disease control

    Last updated Jun 27, 2026 08:03 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space