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

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 journal › Article › peer-review

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 language	English (US)
Pages (from-to)	2-5
Number of pages	4
Journal	Dysmorphology and Clinical Genetics
Volume	2
Issue number	1
State	Published - 1988
Externally published	Yes

ASJC Scopus subject areas

Anatomy
Genetics(clinical)

Cite this

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title = "Cornelia de Lange syndrome with Peters anomaly and fat malabsorption",

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.",

author = "Ponder, {S. W.} and Cynamon, {H. A.} and Isenberg, {J. N.} and Elder, {F. F.B.} and L. Lockhart",

year = "1988",

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AU - Ponder, S. W.

AU - Cynamon, H. A.

AU - Isenberg, J. N.

AU - Elder, F. F.B.

AU - Lockhart, L.

PY - 1988

Y1 - 1988

N2 - 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.

AB - 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.

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JO - Dysmorphology and Clinical Genetics

JF - Dysmorphology and Clinical Genetics

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Cornelia de Lange syndrome with Peters anomaly and fat malabsorption

Abstract

ASJC Scopus subject areas

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