Prune Belly Syndrome

  • JA Hammond
  • EW van den Ende
  • RG Boardman
  • BP Mather

Abstract

Two cases of prune belly syndrome in Black infants are presented. The prune belly syndrome, or congenital absence of abdominal muscles, is accompanied by hydro-ureter, hydronephrosis, megalocystis and usually undescended testes. Other associated congenital defects occur, of which orthopaedic defects appear to be the most prevalent. Others are patent urachus, congenital heart malformation, anomalies of the eyes and ears, ectodermal dysplasia, torticollis and micrognathia.

S. Afr. Med. J., 48, 839 (1974).

Author Biographies

JA Hammond

Department of Paediatrics, Kimberley Hospital, Kimberley, CP

EW van den Ende
Department of Paediatrics, Kimberley Hospital, Kimberley, CP
RG Boardman
Department of Paediatrics, Kimberley Hospital, Kimberley, CP
BP Mather
Department of Paediatrics, Kimberley Hospital, Kimberley, CP
Published
2018-02-18
Section
Articles

Journal Identifiers


eISSN: 0256-95749
print ISSN: 2078-5135