Related Experiment Video For ABCD1
Updated: Oct 13, 2026

An In Vitro Model for the Study of Cellular Pathophysiology in Globoid Cell Leukodystrophy
Published on: October 21, 2014
[X-linked adrenoleukodystrophy: a report of three cases. The importance of early diagnosis]
Marta López Úbeda1, Antonio de Arriba Muñoz2, Marta Ferrer Lozano2
1Unidad de Endocrinología Pediátrica, Hospital Infantil Universitario Miguel Servet, Zaragoza, España. marta.lopez.ubeda@gmail.com.
Abstract:
X-linked adrenoleukodystrophy is the most common peroxisomal disorder. This disease is caused by a defect in the ABCD1 gen. Saturated very long chain fatty acids are accumulated in serum, adrenal cortex and central nervous system white matter. The clinical spectrum is characterized by progressive neurological dysfunction and adrenal insufficiency with a devastating prognosis. We report a first case of X-linked adrenoleukodystrophy with fatal evolution which identified two asymptomatic family members and established a preventive treatment. Although there is no definitive cure, we stress the importance of family study and evaluation of the individual in situation of risk to establish an early preventive treatment and to give in each particular situation suitable professional advice.

