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Sclerocornea associated with the Smith-Lemli-Opitz syndrome.

Abstract：

:A 2,000-g infant boy had many features of the Smith-Lemli-Opitz syndrome (prenatal growth deficiency and developmental retardation, microcephaly with unusual facies, hypospadias, and feeding difficulties) as well as sclerocornea. The association of this rare eye finding with this rare congenital syndrome is unique. Successful penetrating keratoplasty was performed in one eye at 8 months of age.

journal_name

Am J Ophthalmol

journal_title

American journal of ophthalmology

authors

Harbin RL,Katz JI,Frias JL,Rabinowicz IM,Kaufman HE

doi

10.1016/0002-9394(77)90327-0

subject

Has Abstract

pub_date

1977-07-01 00:00:00

pages

72-3

issue

1

eissn

0002-9394

issn

1879-1891

pii

0002-9394(77)90327-0

journal_volume

84

pub_type

杂志文章

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