Cornelia de Lange syndrome with Peters anomaly and fat malabsorption

S. W. Ponder, H. A. Cynamon, J. N. Isenberg, F. F.B. Elder, L. Lockhart

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

A prematurely born male child, subsequently identified as having Cornelia de Lange syndrome, was serially evaluated for failure to thrive and fat malabsorption while undergoing care for congenital corneal opacities (Peters anomaly). Fat malabsorption and Peters anomaly are two newly described manifestations of the Cornelia de Lange syndrome.

Original languageEnglish (US)
Pages (from-to)2-5
Number of pages4
JournalDysmorphology and Clinical Genetics
Volume2
Issue number1
StatePublished - Jan 1 1988

ASJC Scopus subject areas

  • Anatomy
  • Genetics(clinical)

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    Ponder, S. W., Cynamon, H. A., Isenberg, J. N., Elder, F. F. B., & Lockhart, L. (1988). Cornelia de Lange syndrome with Peters anomaly and fat malabsorption. Dysmorphology and Clinical Genetics, 2(1), 2-5.