Cornelia de Lange syndrome with Peters anomaly and fat malabsorption

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

Research output: Contribution to journalArticle

4 Citations (Scopus)

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 - 1988

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De Lange Syndrome
Fats
Corneal Opacity
Failure to Thrive
Peters anomaly

ASJC Scopus subject areas

  • Anatomy
  • Genetics(clinical)

Cite this

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.

Cornelia de Lange syndrome with Peters anomaly and fat malabsorption. / Ponder, S. W.; Cynamon, H. A.; Isenberg, J. N.; Elder, F. F B; Lockhart, Lillian.

In: Dysmorphology and Clinical Genetics, Vol. 2, No. 1, 1988, p. 2-5.

Research output: Contribution to journalArticle

Ponder, SW, Cynamon, HA, Isenberg, JN, Elder, FFB & Lockhart, L 1988, 'Cornelia de Lange syndrome with Peters anomaly and fat malabsorption', Dysmorphology and Clinical Genetics, vol. 2, no. 1, pp. 2-5.
Ponder, S. W. ; Cynamon, H. A. ; Isenberg, J. N. ; Elder, F. F B ; Lockhart, Lillian. / Cornelia de Lange syndrome with Peters anomaly and fat malabsorption. In: Dysmorphology and Clinical Genetics. 1988 ; Vol. 2, No. 1. pp. 2-5.
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