Rare Spontaneous Attenuation of Childhood Inflammatory Cerebral Adrenoleukodystrophy

Author:

Choi Hyoung Won1,Raymond Gerald Vincent2,Miller Weston3

Affiliation:

1. Division of Pediatric Neurology, Department of Neurology, University of Minnesota, Minneapolis, Minnesota, United States

2. Division of Pediatric Neurology, Department of Pediatrics and Neurology, Penn State University, Hershey, Pennsylvania, United States

3. Division of Pediatric Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota, United States

Abstract

AbstractX-linked adrenoleukodystrophy (ALD) is a neurodegenerative peroxisomal disorder with variable clinical phenotypes. Childhood cerebral ALD (CCALD) is at the most severe end of the disease spectrum. In CCALD, the clinical manifestations include increasing deficits in behavior, vision, hearing, coordination, and motor function, as well as seizures. Without treatment, CCALD often results in apparent vegetative state within 1 to 2 years of appearance of initial signs and symptoms. We present the case of a boy with classic inflammatory CCALD who exhibited spontaneous attenuation in disease progression. While extremely rare, spontaneous arrest of disease progression may occur in boys with inflammatory CCALD.

Publisher

Georg Thieme Verlag KG

Subject

Clinical Neurology,Pediatrics, Perinatology, and Child Health

Reference18 articles.

1. Adrenoleukodystrophy: phenotypic variability and implications for therapy;H W Moser;J Inherit Metab Dis,1992

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3. Pathophysiology of X-linked adrenoleukodystrophy;J Berger;Biochimie,2014

4. Arrested cerebral adrenoleukodystrophy: a clinical and proton magnetic resonance spectroscopy study in three patients;G C Korenke;Pediatr Neurol,1996

5. Adrenoleukodystrophy: a scoring method for brain MR observations;D J Loes;Am J Neuroradiol,1994

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