Literature DB >> 9508245

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

R Pallotta1, P Fusilli, G Sabatino, A Verrotti, F Chiarelli.   

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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Year:  1998        PMID: 9508245

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

1.  CRIM1 haploinsufficiency causes defects in eye development in human and mouse.

Authors:  Filippo Beleggia; Yun Li; Jieqing Fan; Nursel H Elcioğlu; Ebru Toker; Thomas Wieland; Irene H Maumenee; Nurten A Akarsu; Thomas Meitinger; Tim M Strom; Richard Lang; Bernd Wollnik
Journal:  Hum Mol Genet       Date:  2015-01-05       Impact factor: 6.150

2.  The familial contribution to non-syndromic ocular coloboma in south India.

Authors:  S J Hornby; L Dandona; R B Jones; H Stewart; C E Gilbert
Journal:  Br J Ophthalmol       Date:  2003-03       Impact factor: 4.638

3.  Inherited partial aniridia, microcornea with high myopia and Bergmeister's papilla: a new phenotypic expression.

Authors:  Prashant Naithani; Ankur Sinha; Viney Gupta
Journal:  Indian J Ophthalmol       Date:  2008 Mar-Apr       Impact factor: 1.848

  3 in total

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