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)|
|Number of pages||4|
|Journal||Dysmorphology and Clinical Genetics|
|State||Published - Jan 1 1988|
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