About The Medical Condition General Peroxisomal Dysfunction
Find the definition of the medical term General Peroxisomal Dysfunction. General Peroxisomal Dysfunction defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
General Peroxisomal Dysfunction
| General Peroxisomal Dysfunction Medical Condition |
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What's The Definition Of The Medical Condition General Peroxisomal Dysfunction?
A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; infantile Refsum disease; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders.
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