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- W2022207498 abstract "R ieger syndrome is a dominantly inherited disorder in which malformation of the anterior chamber of the eye and increased risk for glaucoma is associated with dental anomalies, redundant umbilical skin, and inguinal hernias) Rieger malformation is the term reserved for isolated anterior segment abnormalities without associated systemic abnormalities. Rieger syndrome has been mapped to chromosomal region 4q25 and linked to the epidermal growth factor gene. 2 Rieger syndrome has also been associated with a number of chromosome deletions and trisomies. 2-8 We report an infant with the Rieger malformation and concurrent trisomy 8p." @default.
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- W2022207498 date "1998-02-01" @default.
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- W2022207498 title "Trisomy 8p and Rieger malformation" @default.
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- W2022207498 doi "https://doi.org/10.1016/s1091-8531(98)90113-6" @default.
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