Home LiteratureArticle Details
PMID: 15933890 Published · ppublish English Case Reports Journal Article

Colonic perforation in the first few hours of life associated with rhizomelic chondrodysplasia punctata.

Pediatric surgery international ·Vol. 21 ·No. 8 ·2005-08-00 ·Pages 662-4

Fairbanks T, Emil S

Abstract

Rhizomelic chondrodysplasia punctata (RCP), a rare autosomal recessive disease characterized by a disorder of peroxisome metabolism, has been shown to affect multiple organ systems. A neonate presenting with a colonic perforation in the first few hours of life was subsequently diagnosed with RCP. A literature search revealed no previous reports of intestinal perforation associated with RCP. Intestinal perforation should be added to the list of medical complications associated with RCP.

MeSH Terms
Chondrodysplasia Punctata, Rhizomelic/complications,diagnosis Colonic Diseases/diagnosis,etiology Diagnosis, Differential Fatal Outcome Humans Infant, Newborn Intestinal Perforation/diagnosis,etiology Male
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Fairbanks Timothy
Division of Pediatric Surgery, University of California, Irvine School of Medicine, Bldg. 53, Rt. 81, 101 The City Drive, Orange, CA 92868, USA.
Emil Sherif
References (7)
7 references, click to expand
  1. Natural history of rhizomelic chondrodysplasia punctata.
    Am J Med Genet A. 2003 May 1;118A(4):332-42 PMID: 12687664
  2. Heterogeneity of Chondrodysplasia punctata.
    Humangenetik. 1971;11(3):190-212 PMID: 5544780
  3. PEX7 gene structure, alternative transcripts, and evidence for a founder haplotype for the frequent RCDP allele, L292ter.
    Genomics. 2000 Jan 15;63(2):181-92 PMID: 10673331
  4. Birth prevalence rates of skeletal dysplasias.
    Clin Genet. 1989 Feb;35(2):88-92 PMID: 2785882
  5. Acyl-CoA:dihydroxyacetonephosphate acyltransferase: cloning of the human cDNA and resolution of the molecular basis in rhizomelic chondrodysplasia punctata type 2.
    Hum Mol Genet. 1998 May;7(5):847-53 PMID: 9536089
  6. Ether lipid biosynthesis: alkyl-dihydroxyacetonephosphate synthase protein deficiency leads to reduced dihydroxyacetonephosphate acyltransferase activities.
    J Lipid Res. 1999 Nov;40(11):1998-2003 PMID: 10553003
  7. [Chondrodysplasia punctata (Chondrodystrophia calcificans) II. The rhizomelic type].
    Fortschr Geb Rontgenstr Nuklearmed. 1971 Mar;114(3):327-35 PMID: 4995567
Article Info
Journal
Pediatric surgery international
Abbr.
Pediatr Surg Int
ISSN
0179-0358
Published
2005-08-00
Epub
2005-00-13
Pages
662-4
Language
English
Region
Germany
NLM ID
8609169
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]