A 2-year-old boy presents with hearing impairment, poliosis (a white shock of hair) , complete heterochromia and sectoral heterochromia, hypertelorism, a low hairline with eyebrows that touch in the middle, white pigmentation of the skin, and suspected neurologic deficits. He is diagnosed with Waardenburg syndrome with a mutation in the PAX-3 gene that affects neural crest differentiation. Which of the following structures would most likely also be affected in this patient?
A) Purkinje cells
B) Pyramidal neurons
C) Ventral horns of the spinal cord
D) Astrocytes
E) Neurons and satellite cells of the spinal ganglion
Correct Answer:
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