Short-chain acylCoA dehydrogenase (SCAD) deficiency is a rare mitochondrial disorder involving the beta-oxidation of fatty acylCoA compounds in chains of 4-6 carbons. Unlike other mitochondrial disorders, cases involving autoimmune diseases have not been described. We report a 15-year-old boy with SCAD deficiency who suffered from pernicious anaemia, vitiligo, scleroatrophic lichen and autoimmune thyroiditis. As has been reported in other mitochondrial disorders, we hypothesised that autoimmune diseases are also present in SCAD deficiency. Furthermore, we discuss the possible pathogenetic relationship between these diseases.

Download full-text PDF

Source
http://dx.doi.org/10.1159/000308176DOI Listing

Publication Analysis

Top Keywords

scad deficiency
12
autoimmune thyroiditis
8
pernicious anaemia
8
anaemia vitiligo
8
vitiligo scleroatrophic
8
scleroatrophic lichen
8
short-chain acylcoa
8
acylcoa dehydrogenase
8
mitochondrial disorders
8
autoimmune diseases
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!