Skip to main navigation Skip to search Skip to main content

DAS KAMPOMELE SYNDROM

Translated title of the contribution: Campomelic syndrome
  • M. R. Ameri
  • , M. Alebouyeh
  • , M. Amirfeyz
  • , M. Ziai
  • , M. R. Rafii
  • , A. Gandjour

Research output: Contribution to journalArticlepeer-review

Abstract

A female premature infant with dwarfism, peculiar facial features, cleft palate and bone anomalies including bowing of the lower extremities with pretibial skin dimpling, the so called 'campomelic syndrome' is presented. Other symptoms were hypotonia and respiratory distress. The radiological and autopsy findings in this child are described. The lack of known teratogenic factors during the pregnancy and the available data about the familial occurrence of this malformation syndrome suggest the possibility of an autosomal recessive mode of inheritance in this patient. This is the first case of campomelic syndrome reported from Iran.

Translated title of the contributionCampomelic syndrome
Original languageGerman
Pages (from-to)687-689
Number of pages3
JournalMonatsschrift fur Kinderheilkunde
Volume126
Issue number11
StatePublished - 1978

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Surgery

Fingerprint

Dive into the research topics of 'Campomelic syndrome'. Together they form a unique fingerprint.

Cite this