USMLE® Step 1 style questions USMLE
A 24-year old man presents to his primary care physician’s clinic due to increasing weakness in his legs for the last three years. He notes that his legs feel very stiff. He reports that he had a maternal uncle with similar issues. On physical exam, the patient has decreased vibratory sensation in the bilateral lower extremities. He exhibits signs of early male pattern baldness. The physician confirms the suspected diagnosis via testing the patient’s plasma for accumulated very-long-chain fatty acids (VLCFA) and a mutation in the ABCD1 gene. Which of the following organelles is affected in this patient’s disease?
Myelin refers to the electrical insulation sheath around axons which allows neurons to quickly send electrical impulses to one another.
Leukodystrophy is a dysmyelinating disease, meaning the structure of the myelin is abnormal, and it’s usually due to a genetic mutation.
In contrast, in a demyelinating diseases, previously normal myelin is damaged, like in multiple sclerosis where the immune cells attack the myelin.
The cerebral cortex is the largest region of the brain and it’s responsible for sensory and motor functions.
The cerebral cortex has an outer grey area and an inner white area.
The grey area, referred to as grey matter, houses neuron cell bodies.
And the white area, referred to as white matter, houses myelinated axons.
It is lighter because of the high fat content in myelin.
Neurons are the key cells that transmit neural impulses to one another through synapses.
Each neuron has dendrites, a cell body, and an axon.
Dendrites are the branches that first receive a neural impulse at a synapse with another neuron.
Myelin is a specialized membrane which helps insulate the axon to make neural impulses travel faster.
Now the myelin is composed of certain fats, and the primary fat is called galactocerebroside.
Galactocerebroside is also used to make another fat found in myelin called cerebroside sulfatide.
One enzyme that’s found in the lysosome is galactosylceramidase, which is encoded by the GALC gene.
Galactosylceramidase helps break down galactocerebroside as well as a cytotoxic metabolite called psychosine, which is a by-product of myelin production.
Another enzyme that’s in the lysosome is cerebroside-sulfatase, which is encoded by the arylsulfatase A gene, and helps break down cerebroside sulfatide.
Most leukodystrophies are caused by genetic mutations and follow an autosomal recessive inheritance patterns, but some like Adrenoleukodystrophy are X-linked recessive. Let’s go through three of the most common ones.
First off, there’s Krabbe disease, named after the Danish neurologist Knud Krabbe, and it originates from a mutation in the GALC gene, which results in a shortage of galactosylceramidase.
Leukodystrophy refers to a group of dysmyelinating diseases of the central and peripheral nervous system caused by genetic mutations in enzymes necessary for myelin production. The most common types are metachromatic leukodystrophy, Krabbe disease, and adrenoleukodystrophy. Symptoms are due to neurodegeneration, like decreased motor function, muscular rigidity, and later, blindness and hearing loss.