Clinical features
Mutations in EOGT cause cause Adams-Oliver syndrome-4, a disorder characterized by congenital absence of skin (usually of the scalp) and absence or underdevelopment of parts of the limbs. Other abnormalities may also be present and could affect the heart and the brain.
Prevalence
Largely unknown due to limited data.
Inheritance
Mutations of this gene can be passed on to the next generation in an autosomal recessive manner. This means that if both parents carry a mutation involving this gene (usually without displaying the disease), there is a greater chance that their children are going to inherit the mutations from both parents and display the disease. This is especially important to consider in consanguineous marriage, where the chance of both parents having the same mutation and passing it is greater.