leukodystrophy

In a leukodystrophy, there are problems with the growth or the development of this cover.

Provides information and resources for leukodystrophy patients and their families.

More often than not, it is simply classified as a non-specific leukodystrophy.

The individual articles on each leukodystrophy will describe the particular pattern of inheritance for that disease.

The author created the character, Android, from a child born with a genetic anomaly called leukodystrophy.

To the parents of a child in the advanced stages of still another leukodystrophy: Prepare for what comes after the end.

Thus leukodystrophy describes a set of diseases that affect the growth or maintenance of the white matter.

Android, Age One is a science fiction adventure based on the real life and death of a child with leukodystrophy.

The most common symptom of a leukodystrophy disease is a gradual decline in an infant or child who previously appeared well.

Symptoms vary according to the specific type of leukodystrophy, and may be difficult to recognise in the early stages of the disease.

In addition, many research groups are studying the cellular processes of myelination, which may provide insights into leukodystrophy.

In some patients, a progressive leukodystrophy has been observed that has a variable age of onset.

An inherited genetic problem that exists in the breed is globoid cell leukodystrophy.

ELA is thus a bridge between all forms of leukodystrophy and a family solidarity network.

Leukodystrophy causes a disruption to the myelin covering that protects nerves.

Its presence is associated with either pilocytic astrocytoma (more common) or Alexander's disease (a rare leukodystrophy).

They may be inherited in a recessive, dominant, or X-linked manner, depending on the type of leukodystrophy.

The word leukodystrophy comes from the Greek roots leuko, white, dys, lack of, and troph, growth.

A deficiency is associated with metachromatic leukodystrophy.

Metachromatic leukodystrophy and multiple sulfatase deficiency are classified as sulfatidoses.

Mutations in this gene have been associated with Krabbe disease, also known as globoid cell leukodystrophy.

Krabbe's Leukodystrophy is inherited as an autosomal recessive trait.

Leukodystrophy refers to a group of disorders characterized by dysfunction of the white matter of the brain.

VWM is a leukodystrophy which has unique biochemical abnormalities.

Leukodystrophy is a gene defect.