Myasthenia Gravis is primarily associated with which of the following?

Prepare for the ASCP Pathology Assistant Exam. Study effectively with our diverse question formats, receive detailed explanations, and confidently advance towards your certification. Boost your readiness now!

Myasthenia Gravis is primarily characterized by an autoimmune response that targets and leads to the loss of acetylcholine receptors at the neuromuscular junction. In this condition, antibodies are formed against the nicotinic acetylcholine receptors, preventing acetylcholine from binding effectively and thus inhibiting muscle contraction. This impaired communication between nerves and muscles results in the hallmark symptoms of muscle weakness and fatigue that worsen with activity.

The underlying mechanism involves a reduction in the number of functional acetylcholine receptors, contributing to muscle weakness. Patients with Myasthenia Gravis often improve with treatments that increase the availability of acetylcholine or reduce antibody production, further underscoring the importance of the autoimmune nature of the disease.

Other options, such as genetic defects in muscle fibers, pertain to different types of myopathies, while increased neurotransmitter release would not align with the pathophysiology of Myasthenia Gravis. Moreover, reactive hyperplasia of nerve cells does not directly relate to the autoimmune mechanism causing the loss of receptors in this condition.

Subscribe

Get the latest from Examzify

You can unsubscribe at any time. Read our privacy policy