Format

Send to

Choose Destination
J Inherit Metab Dis. 2007 Apr;30(2):193-7. Epub 2007 Mar 8.

Molecular and clinical aspects of peroxisomal diseases.

Author information

1
Division of Genomics Research, Life Science Research Center, Gifu University, Yanagido 1-1, Gifu, 501-1193, Japan. nshim@gifu-u.ac.jp

Abstract

Peroxisomal diseases, an expanding group of inborn errors of metabolism, can be classified into three categories--peroxisome biogenesis disorders (PBDs), single peroxisomal enzyme deficiencies, and contiguous gene syndrome. PBDs comprise 13 complementation groups and their responsible genes have been identified, including our newly identified group with a PEX14 defect. We have established a diagnostic system of peroxisomal diseases in Japan, and have identified 40 Japanese with PBDs, 11 patients with beta-oxidation enzyme deficiencies and more than 100 patients with adrenoleukodystrophy. Further study of and enlightenment on peroxisomal diseases is necessary to overcome these disorders.

PMID:
17347916
DOI:
10.1007/s10545-007-0516-z
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Wiley
Loading ...
Support Center