As for other autosomal recessive diseases, the recurrence risk for each subsequent child of the same parents is 25%.

This phenomenon may maintain and possibly even increase the incidence of autosomal recessive disease.

From an evolutionary perspective, a recessive disease or trait can remain hidden for several generations before displaying the phenotype.

Since the disorder is X-linked recessive the disease affects more males.

This is known as an autosomal recessive disease.

As we will see, mutations that cause recessive diseases result in the loss of these neuroprotective functions.

It is classified as an autosomal recessive disease, one that can be passed down through the generations.

There may also be other deleterious effects besides those caused by recessive diseases.

It is a rare, hereditary recessive autosomal disease, in general, diagnosed during childhood.

Three rare recessive diseases in humans have been shown to be caused by genes of this family.