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Hallermann-Streiff syndrome associated with sclerocornea, aniridia, and a chromosomal abnormality.

作者信息

Schanzlin D J, Goldberg D B, Brown S I

出版信息

Am J Ophthalmol. 1980 Sep;90(3):411-5. doi: 10.1016/s0002-9394(14)74926-8.

DOI:10.1016/s0002-9394(14)74926-8
PMID:6999913
Abstract

An infant with the features of Hallermann-Streiff syndrome also had the previously unreported ocular signs of sclerocornea, buphthalmos, congenital glaucoma, and aniridia. Chromosome analysis revealed an elongation of one of the arms of the tenth chromosome. The infant was the product of a consanguinous marriage between distant cousins and a distant cousin of the patient also had the typical features of the Hallermann-Streiff syndrome.

摘要

相似文献

1
Hallermann-Streiff syndrome associated with sclerocornea, aniridia, and a chromosomal abnormality.
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Congenital cataracts in mother, sister, and son of a patient with Hallermann-Streiff syndrome: coincidence or clue?一名患有哈勒曼-施特雷夫综合征患者的母亲、姐姐和儿子患有先天性白内障:巧合还是线索?
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