NLM Logo

Peroxisome biogenesis disorders MeSH Supplementary Concept Data 2023


MeSH Supplementary
Peroxisome biogenesis disorders
Unique ID
C536664
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C536664
Registry Number
0
Heading Mapped to
*Peroxisomal Disorders
Frequency
57
Note
The peroxisome biogenesis disorders (PBDs) neonatal adrenoleukodystrophy (NALD) and infantile Refsum disease (IRD) represent the milder manifestations of the ZELLWEGER SYNDROME SPECTRUM. Most patients survive to adolesence and affected children experience HYPOTONIA but are able to achieve developmental milestones. In addition, craniofacial features are similar to but less pronounced than in Zellweger syndrome. Patients also may experience SEIZURES. and have renal cysts. In contrast to ZS, they may also develop SENSORINEURAL HEARING LOSS and RETINITIS PIGMENTOSA. Caused by mutations in the PEX genes. OMIM: 601539
Date of Entry
2010/08/25
Revision Date
2015/08/18
Peroxisome biogenesis disorders Preferred
page delivered in 0.005s