Glossary/Terms

We have compiled a list of words that you may encounter when reading information on Leukodystrophy. Please let us know if there are any words that you would like us to add.

Allele

One member of a pair of genes that occupy a specific position on a specific chromosome.

Anosmia

Loss of the sense of smell.

Arteriopathy

disease of the arteries.

Asparatoacylase

the gene responsible for Canavan disease. It is involved in the breakdown of a molecule called NAA, a molecule that is thought to be involved in the removal of water from certain types of brain cells, as well as in the formation of myelin lipids.

Astrocyte

a type of glial cell that provides physical and nutritional support for neurons. Their primary functions include cleaning up brain “debris,” transporting nutrients to neurons, and holding neurons in place

Ataxia

disturbance of gait or coordination

Autosome

all of the chromsomes that are not the sex chromosomes

Axon

a physical projection of the neuron cell body that is responsible for carrying signals away from the neuron.

Cataract

clouding over the lens of the eye, impairs normal vision
Central nervous system: consists of the brain and the spinal cord. It controls thought processes, guides movement, and registers sensations throughout the body.

Cerebellar ataxia

axia is wobbliness. Cerebellar ataxia refers to the fact that the defect is in a specific part of the brain (the cerebellum), and the incoordination and unsteadiness is due to the brain’s failure to regulate the body’s posture, as well as the strength and direction of the body’s movements.

Chromosome

a linear strand of DNA that contains many genes; there are 46 human chromosomes (22 pairs of chromsomes, and the X and Y chromosomes).

Craniofacial dysmorphism

refers to an abnormality of the face and/or the head. Craniofacial dysmorphism can include abnormal growth patterns of the face or skull, and may involve the soft tissue as well as the bones. In the case of 18q-syndrome, craniofacial abnormalities will most likely include deep-set eyes, a “carp-shaped” mouth, microcephaly (small head), prominent ears, and midfacial hypoplasia (underdeveloped midfacial regions).

Dendrite

a physical projection of the neuron cell body that is responsible for carrying signals to the neuron.

Dominant Inheritance

a method of genetic inheritance, whereby a single abnormal copy of a gene causes disease, even though a good copy of the gene is also present.

Dystonia

neurological disorder characterized by involuntary muscle contractions; can affect any part of the body

Epiphyseal dysplasia

The epiphysus is the growth area at the end of a bone, while dysplasia means abnormal formation. This means that patients with Refsum disease often have shortened limbs.

Epicanthus

a fold of skin that comes in across the inner angle of the eye, common in children with birth defects such as Down syndrome

Failure to thrive

A general term meaning the child is not growing and gaining weight at the expected rate;

FISH

see Fluorescent in situ Hybridization

Fluorescent in situ Hybridization (FISH)

a method of visualizing chromosomes that can allow scientists to look for gross chromosomal abnormalities

Fontanelle

the baby’s “soft spot”

Galactocerebrosidase

Also called GALC, this is the protein responsible for

Genu recurvatum:

Genital hypoplasia

incomplete development of the genitals

Glaucoma

An eye condition in which the fluid pressure inside the eyes is high, may damage the eye, leading to vision loss

Glial cell

a specialized type of cell that is a “helper” to neurons, and is necessary for the proper function of the nervous system. There are several types of glial cells, including astrocytes, microglia, oligodendroglia, satellite cells, and Schwann cells (see the individual defintions of these subtypes of glial cells for more information)

Globoid cells

a specific type of cell (called the macrophage) accumulates high levels of undegraded galactolipids as a result of the lack of GALC activity in globoid cell leukodystrophy. These cells look different from healthy cells, and are termed globoid cells.

granular osmiophilic material

Also called GOM, it is a granular material that accumulates in patients with CADASIL disease.

Hepatomegaly

enlarged liver

Hydrocephaly

Literally means “water on the brain.” Characterized by the accumulation of fluid in the brain or between the brain and the skull. Can cause pressure on the brain, resulting in developmental defects. Also can lead to an abnormally large head size (to greater than 90% of normal).

Hyperextension of the limbs

limbs are kept abnormally straight

Hyporeflexia

slow reflexes

Hypotonia

Poor muscle tone

Icthyosis

Icthyosis is a noninflammatory scaliness of the skin. These symptoms can range anywhere from scaliness of the palms and soles of the feet to scaliness on the trunk of the body.

Infarcts

areas of tissue that have undergone a type of cell death called necrosis, as a result of restricted blood supply.
Ischemic episodes

resulting from low oxygen in the blood or tissues, generally as a result of an obstruction of the arterial blood flow.

Leukodystrophy

The word leukodystrophy comes from the Greek words leuko (meaning white), trophy (meaning growth), and dys (meaning ill). If you put these words together, the word leukodystrophy describes a set of diseases that affect the growth or maintenance of the white matter (myelin).

Leukoencephalitis:

Leukoencephalopathy

a type of change associated with the white matter, which includes localized areas of cell death.

Magnetic Resonance Imaging (MRI)

An imaging technique that can be used to visualize any/all parts of the body. The scan is painless and does not involve radiation.

MBP

See Myelin basic Protein

Macroencaphaly

abnormally large brain; this can lead to delayed development, convulsive disorders, corticospinal (brain cortex and spinal cord) dysfunction, and seizures. Also called Megalencephaly.

Megalencephaly

abnormally large brain; this can lead to delayed development, convulsive disorders, corticospinal (brain cortex and spinal cord) dysfunction, and seizures. Also called Macroencephaly.

Microglia

a type of glial cell that is involved in the digestion of dead neurons.

Micrognathia

small chin

Migraine with aura

a migraine is a vascular headache resulting from changes in the sizes of the arteries in the brain. An aura refers to an abnormal sensation that the migraine is going to occur.

Muscle flexion

Muscles tend to be kept flexed

Myelin

Myelin, sometimes referred to as “white matter” because of its white, fatty appearance, protects and insulates the axons. It consists of a protective sheath of many different molecules that include both lipids (fatty molecules) and proteins. This protective sheath acts in a manner very similar to that of the protective insulation that surrounds an electric wire; that is, it is necessary for the rapid transmission of electrical signals between neurons. It does this primarily by containing the electrical molecules (called ions) within the axon so that they are properly transmitted to the next neuron.

Myelin Basic Protein (MBP)

the gene thought to be responsble for 18q-Syndrome, or at least for the leukodystrophy aspects of the syndrome.
N-acetyl-L-aspartate

Also called NAA., this molecule is involved in the removal of water from certain types of brain cells, as well as in the formation of myelin lipids. It is involved in the pathology of Canavan Disease.

Neuron

also called a “nerve cell,” the neurons are responsible for transmitting messages throughout the body. They are important in both involuntary functions (like your heartbeat) and voluntary functions (like walking).

Notch3

the gene responsible for CADASIL disease, which is involved in determining cell fate

Nystagmus

rapid rhythmic repetitious involuntary eye movements

Occiput

The occiput is the bone forming the back of the skull, and encloses the hole where the spinal cord reaches the brain

Oligodendroglia

a type of glial cell that provides the insulation (myelin) to neurons in the central nervous system.

Orbital ridge

the bony ridge beneath the eyebrow

Peripheral nervous system

consists of the neurons throughout the body with the exception of those in the CNS. These include the sensory neurons, which detect any sensory stimuli and alert the CNS of their presence, and motor neurons, which connect the CNS to the muscles and carry out instructions from the CNS for movement.

Peroxisome

a membrane-bound compartment in the cell that is responsible for the breakdown of certain types of fatty acids

Peripheral polyneuropathy

is the term for dysfunction of the nerves outside of the spinal cord. Symptoms may include numbness, weakness, burning pain, and loss of reflexes.

Quadriplegia

complete paralysis of the body from the neck down

Recessive inheritance

A mode of genetic inheritance whereby an affected person must have two dysfunctional forms of the gene to have the disease. Practically, this means that two parents could

Retinitis pigmentosa

a disease of the eye, resulting from degeneration of a part of the eye called the retina. It affects night vision and peripheral vision, and eventually can lead to blindness.

Rosenthal fibers

abnormal, fibrous deposits present in the CNS that are characteristic of Alexander Disease

Satellite cells

a type of glial cell that provides physical support to the neurons.

chawann cells

a type of glial cell that provides the insulation (myelin) to neurons in the peripheral nervous system.

Seizure

The brain controls how the body moves by sending electrical signals. Seizures (also called convulsions) occur when the normal signals from the brain are changed. Severity of a seizure can vary dramatically. Some people may only shake slightly and do not lose consciousness. Other people may become unconscious and have violent shaking of the entire body.

Spasticity

tendency to have involuntary muscle contractions

Subcortical

relating to the portion of the brain immediately below the cerebral cortex, which is the part of the brain responsible for most higher functions (sensation, voluntary muscle movement, thought, reasoning, memory, etc.)

X-linked inheritance

A mode of genetic inheritance where the gene responsible for the disease is located on the X chromosome. Practically, this means that men are more likely to have the disease than women. Please see our fact sheet on genetic inheritance for more information.