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Ophthalmic Paediatrics and Genetics Volume 13, 1992 - Issue 3
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Original Article

Congenital glaucoma in a child with partial lq duplication and 9p deletion

Frank D. Verbraak Department of Ophthalmogenetics, The Netherlands Ophthalmic Research Institute, Amsterdam
,
Katalin Pogány Department of Ophthalmogenetics, The Netherlands Ophthalmic Research Institute, Amsterdam
,
Jan-Willem Pilon Department of Paediatrics, Zuiderzee Ziekenhuis, Lelystad
,
C. m. Mooy Department of Clinical Pathology, Erasmus University Rotterdam, Rotterdam
,
H. F. De France Clinical Genetics Center Utrecht, Utrecht, The Netherlands
,
Raoul C.m. Hennekam Clinical Genetics Center Utrecht, Utrecht, The Netherlands
&
E. M. Bleeker-Wagemakers Department of Ophthalmogenetics, The Netherlands Ophthalmic Research Institute, Amsterdam
 show all
Pages 165-170 | Accepted 02 Jun 1992, Published online: 08 Jul 2009

Citations (8)

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Read on this site (2)

Konal Saha, Ian Christopher Lloyd, Isabelle Mary Russell-Eggitt & David Samuel Irving Taylor. (2007) Chromosomal Abnormalities and Glaucoma: A Case of Congenital Glaucoma Associated with 9p Deletion Syndrome. Ophthalmic Genetics 28:2, pages 69-72.
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Amy C. Cohn, Lisa S. Kearns, Ravi Savarirayan, Jacinta Ryan, Jamie E. Craig & David A. Mackey. (2005) Chromosomal Abnormalities and Glaucoma: A Case of Congenital Glaucoma with Trisomy 8q22-Qter/ Monosomy 9p23-Pter. Ophthalmic Genetics 26:1, pages 45-53.
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Articles from other publishers (6)

Mario Zanolli, Alex V. Levin & Guillermo Lay-Son. 2017. The Eye in Pediatric Systemic Disease. The Eye in Pediatric Systemic Disease 109 170 .
Zeynep Aktas, Emine Esra Karaca, Nurcan Dogan, Tugba ?akmak, Metin Unlu, Levent Tok & Murat Hasanreisoglu. (2013) Congenital glaucoma as an ophthalmic manifestation of Frank?Ter Haar syndrome. International Ophthalmology 34:2, pages 351-354.
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Ibrahim Akalin, Senol Bozdag, Malte Spielmann, Sarenur Yilmaz Basaran, Indrajit Nanda & Eva Klopocki. (2014) Partial trisomy 1q41-qter and partial trisomy 9pter-9q21.32 in a newborn infant: An array CGH analysis and review. American Journal of Medical Genetics Part A 164:2, pages 490-494.
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Valérie Senée, Claude Chelala, Sabine Duchatelet, Daorong Feng, Hervé Blanc, Jack-Christophe Cossec, Céline Charon, Marc Nicolino, Pascal Boileau, Douglas R Cavener, Pierre Bougnères, Doris Taha & Cécile Julier. (2006) Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism. Nature Genetics 38:6, pages 682-687.
Crossref
J. Bronwyn Bateman. 2006. Handbook of Pediatric Eye and Systemic Disease. Handbook of Pediatric Eye and Systemic Disease 76 145 .
J. Bronwyn Bateman. 2003. Pediatric Ophthalmology and Strabismus. Pediatric Ophthalmology and Strabismus 675 704 .

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