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In roughly 36% of cases, the cause is never identified (idiopathic gastroparesis)

Neurologically, ALD/AMN can manifest with highly variable phenotypes, ranging from very aggressive and rapidly fatal inflammatory CNS demyelination in young boys to a more slowly progressive adult form either with cerebral white matter inflammatory lesions, or a more indolent progressive myelopathy and peripheral neuropathy (Moser, 1997)

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Acknowledgments We would like to thank all colleagues and mentors for their assistance