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Adrenoleukodystrophy |
Credits: 1.25 Post-Assessment Questions: 12
Release Date: 5 Oct 2020
Expiration Date: 3 Mar 2022
Last Reviewed: 3 Mar 2021
Estimated Time To Finish: 75 Minutes
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Adrenoleukodystrophy is a peroxisomal disorder resulting from abnormal metabolism of the very-long-chain fatty acids (VLCFA). It is classified into different subtypes based on the mode of inheritance, clinical presentation, age of onset, and organs involved. The prognosis is poor, and the majority of affected patients will develop neurological disabilities and death. This activity reviews the pathophysiology, evaluation, management, and prognosis of the different adrenoleukodystrophy types and highlights the new updates about the diagnosis and treatment options that are available or under investigation for this condition.
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Authors: Mahdi Alsaleem
Editors: Lina Saadeh
Editors-In-Chief: William GossmanDivyesh Nemakayala
Chief Medical Reviewer: Mahdi Alsaleem
Nurse Planner/Reviewer/Editor: Lisa Haddad
Nurse Planner/Reviewer/Editor: Bernadette Makar
Nurse Planner/Reviewer/Editor: Dorothy Caputo
Pharmacy Planner/Reviewer/Editor: Mark Pellegrini
Physician Planner/Reviewer/Editor: Scott Dulebohn
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Quillen College of Medicine, East Tennessee State University designates this activity for a maximum of 1.25 AMA PRA Category 1 CreditsTM. Physicians should only claim credit commensurate with the extent of their participation in the activity.
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