Literature DB >> 15933890

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

Timothy Fairbanks1, Sherif Emil.   

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.

Entities:  

Mesh:

Year:  2005        PMID: 15933890     DOI: 10.1007/s00383-005-1426-5

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  7 in total

1.  Natural history of rhizomelic chondrodysplasia punctata.

Authors:  Amy L White; Peggy Modaff; Francesca Holland-Morris; Richard M Pauli
Journal:  Am J Med Genet A       Date:  2003-05-01       Impact factor: 2.802

2.  Birth prevalence rates of skeletal dysplasias.

Authors:  C Stoll; B Dott; M P Roth; Y Alembik
Journal:  Clin Genet       Date:  1989-02       Impact factor: 4.438

3.  Heterogeneity of Chondrodysplasia punctata.

Authors:  J W Spranger; J M Opitz; U Bidder
Journal:  Humangenetik       Date:  1971

4.  [Chondrodysplasia punctata (Chondrodystrophia calcificans) II. The rhizomelic type].

Authors:  J W Spranger; U Bidder; C Voelz
Journal:  Fortschr Geb Rontgenstr Nuklearmed       Date:  1971-03

5.  Ether lipid biosynthesis: alkyl-dihydroxyacetonephosphate synthase protein deficiency leads to reduced dihydroxyacetonephosphate acyltransferase activities.

Authors:  E C de Vet; L Ijlst; W Oostheim; C Dekker; H W Moser; H van Den Bosch; R J Wanders
Journal:  J Lipid Res       Date:  1999-11       Impact factor: 5.922

6.  PEX7 gene structure, alternative transcripts, and evidence for a founder haplotype for the frequent RCDP allele, L292ter.

Authors:  N Braverman; G Steel; P Lin; A Moser; H Moser; D Valle
Journal:  Genomics       Date:  2000-01-15       Impact factor: 5.736

7.  Acyl-CoA:dihydroxyacetonephosphate acyltransferase: cloning of the human cDNA and resolution of the molecular basis in rhizomelic chondrodysplasia punctata type 2.

Authors:  R Ofman; E H Hettema; E M Hogenhout; U Caruso; A O Muijsers; R J Wanders
Journal:  Hum Mol Genet       Date:  1998-05       Impact factor: 6.150

  7 in total
  1 in total

1.  Predicting the impact of diet and enzymopathies on human small intestinal epithelial cells.

Authors:  Swagatika Sahoo; Ines Thiele
Journal:  Hum Mol Genet       Date:  2013-03-13       Impact factor: 6.150

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.