Dysfunction, Single Peroxisomal Medical Condition Defined & Explained

About The Medical Condition Dysfunction, Single Peroxisomal

Find the definition of the medical term Dysfunction, Single Peroxisomal. Dysfunction, Single Peroxisomal defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.

Dysfunction, Single Peroxisomal

Dysfunction, Single Peroxisomal Medical Condition
What's The Definition Of The Medical Condition Dysfunction, Single Peroxisomal? 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.

Dysfunction, Single Peroxisomal Medical Condition

What's The Definition Of The Medical Condition Dysfunction, Single Peroxisomal?

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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