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Confirmation of the colobomatous macrophthalmia with microcornea syndrome: report of another family.

作者信息

Pallotta R, Fusilli P, Sabatino G, Verrotti A, Chiarelli F

机构信息

Center for Diagnosis, Prevention and Care of Birth Defects, Department of Medicine, G. D'Annunzio University, Chieti, Italy.

出版信息

Am J Med Genet. 1998 Mar 19;76(3):252-4.

PMID:9508245
Abstract

We report on the occurrence of microcornea, coloboma, and macrophthalmia in 4 generations of an Italian family. The patients had no additional physical anomalies, were of normal intelligence, and had a normal karyotype. This condition has been reported in only 1 family [Bateman and Maumenee, 1984: Ophthalmol Pediatr Genet 4:59-66]. The recurrence of this distinctive ocular pattern in our opinion confirms the existence of a new syndrome, with autosomal dominant inheritance.

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