Zellweger Syndrome: A Downs Syndrome Mimic

  • Dr. Tanmay Khadpe TN Medical College and BYL Nair Hospital, Mumbai Central, Mumbai, India.
  • Dr. Alpana Kondekar TN Medical College and BYL Nair Hospital, Mumbai Central, Mumbai, India.
  • Dr. Varun Anand TN Medical College and BYL Nair Hospital, Mumbai Central, Mumbai, India.
  • Dr. Radha Ghildiyal TN Medical College and BYL Nair Hospital, Mumbai Central, Mumbai, India.
Keywords: Peroxisomal diseases, PEX genes, Zellweger spectrum disorders, Very long chain fatty acids, Plasmalogens, Downs Syndrome

Abstract

The peroxisomal diseases are genetically determined disorders caused either by the failure to form or maintain the peroxisome or by a defect in the function of a single protein that is normally located in this organelle. It is a heterogeneous group of autosomal recessive disorders characterized by a defect in peroxisome formation and are caused by mutations in one of 13 PEX genes. The defect in peroxisome formation or impaired metabolic pathways result in metabolic abnormalities. Typically in Zellweger spectrum disorders (ZSD) patients accumulate very long chain fatty acids (VLCFAs), phytanic and pristanic acid, C27-bile acid intermediates and pipecolic acid in plasma and have a deficiency of plasmalogens in erythrocytes.These disorders present with a wider range of phenotype than has been recognized in the past and few of them may phenotypically resemble Downs Syndrome.

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References

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Zellweger Syndrome: A Downs Syndrome Mimic
CITATION
DOI: 10.17511/ijpr.2019.i02.05
Published: 2019-02-28
How to Cite
Dr. Tanmay Khadpe, Dr. Alpana Kondekar, Dr. Varun Anand, & Dr. Radha Ghildiyal. (2019). Zellweger Syndrome: A Downs Syndrome Mimic. Pediatric Review: International Journal of Pediatric Research, 6(2), 76-80. https://doi.org/10.17511/ijpr.2019.i02.05
Section
Case Report