Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency.

Abstract

An infant with the characteristic phenotype of classical rhizomelic chondrodysplasia punctata was found to have an isolated deficiency of the peroxisomal enzyme acyl CoA dihydroxyacetone phosphate acyltransferase (DHAP-AT). All other peroxisomal functions measured were found to be normal. Previously described in one other case report, this confirms the existence of another distinct form of peroxisomal disorder characterised biochemically by a deficiency in de novo plasmalogen biosynthesis only.

• Authors: D G Barr, J M Kirk, M al Howasi, R J Wanders, R B Schutgens
• Journal: Archives of disease in childhood (Arch Dis Child) Vol. 68 Issue 3 Pg. 415-7 (Mar 1993) ISSN: 1468-2044 [Electronic] England
• PMID: 8466247 (Publication Type: Case Reports, Journal Article)

Chemical References

• Plasmalogens
• Acyltransferases
• glycerone-phosphate O-acyltransferase

Topics

• Acyltransferases (deficiency)
• Chondrodysplasia Punctata (enzymology)
• Fibroblasts (metabolism)
• Humans
• Infant, Newborn
• Male
• Microbodies (metabolism)
• Phenotype
• Plasmalogens (biosynthesis)