Stickler and Marshall syndromes: Additional evidence for their identity

A. Rossodivita, G. Zampino, F. Balducci, M. Macchiaiolo, P. Giordano, F. Colabucci, P. Mastroiacovo

Research output: Contribution to journalArticle

Abstract

We report on a girl with manifestations of Marshall syndrome and Stickler syndrome, supporting the hypothesis that they are not separate entities but variable expressions of the same inherited condition. Moreover, this is the first reported case in which a growth hormone deficiency has been documented.

Original languageEnglish
Pages (from-to)154-156
Number of pages3
JournalRivista Italiana di Pediatria
Volume23
Issue number1
Publication statusPublished - Feb 1997

Keywords

  • Growth hormone deficiency
  • Hereditary arthroophtalmopathy
  • Marshall syndrome
  • Stickler syndrome

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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    Rossodivita, A., Zampino, G., Balducci, F., Macchiaiolo, M., Giordano, P., Colabucci, F., & Mastroiacovo, P. (1997). Stickler and Marshall syndromes: Additional evidence for their identity. Rivista Italiana di Pediatria, 23(1), 154-156.