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Ophthalmic Genetics Volume 23, 2002 - Issue 4
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Research Article

Evidence of clinical and genetic heterogeneity in autosomal dominant congenital cerulean cataracts

Latifa Hilal Laboratoire de Genetique et Biologie Moleculaire de la Faculte des Sciences, Universite IBN Tofail, Kenitra, and Departement d'Oto-Neuro-Ophtalmologie, Service d'Ophtalmologie B, Hopital des Specialites, Rabat, Morocco
,
Emeline Nandrot Centre de Recherches Therapeutiques en Ophtalmologie de la Faculte de Medecine Necker, EA n°2502 du Ministere de la Recherche et de l'Enseignement Superieur, Universite Rene Descartes, Paris, and Unite INSERM 423, CHU Necker-Enfants Malades, Paris, France
,
Mohamed Belmekki Laboratoire de Genetique et Biologie Moleculaire de la Faculte des Sciences, Universite IBN Tofail, Kenitra, and Departement d'Oto-Neuro-Ophtalmologie, Service d'Ophtalmologie B, Hopital des Specialites, Rabat, Morocco
,
Mohamed Chefchaouni Laboratoire de Genetique et Biologie Moleculaire de la Faculte des Sciences, Universite IBN Tofail, Kenitra, and Departement d'Oto-Neuro-Ophtalmologie, Service d'Ophtalmologie B, Hopital des Specialites, Rabat, Morocco
,
Siham El Bacha Laboratoire de Genetique et Biologie Moleculaire de la Faculte des Sciences, Universite IBN Tofail, Kenitra, and Departement d'Oto-Neuro-Ophtalmologie, Service d'Ophtalmologie B, Hopital des Specialites, Rabat, Morocco
,
Bouchra Benazzouz Laboratoire de Genetique et Biologie Moleculaire de la Faculte des Sciences, Universite IBN Tofail, Kenitra, and Departement d'Oto-Neuro-Ophtalmologie, Service d'Ophtalmologie B, Hopital des Specialites, Rabat, Morocco
,
Yassir Hajaji Laboratoire de Genetique et Biologie Moleculaire de la Faculte des Sciences, Universite IBN Tofail, Kenitra, and Departement d'Oto-Neuro-Ophtalmologie, Service d'Ophtalmologie B, Hopital des Specialites, Rabat, Morocco
,
Olivier Gribouval Centre de Recherches Therapeutiques en Ophtalmologie de la Faculte de Medecine Necker, EA n°2502 du Ministere de la Recherche et de l'Enseignement Superieur, Universite Rene Descartes, Paris, and Unite INSERM 423, CHU Necker-Enfants Malades, Paris, France
,
Jean-Louis Dufier Centre de Recherches Therapeutiques en Ophtalmologie de la Faculte de Medecine Necker, EA n°2502 du Ministere de la Recherche et de l'Enseignement Superieur, Universite Rene Descartes, Paris, and Unite INSERM 423, CHU Necker-Enfants Malades, Paris, France
,
Marc Abitbol Centre de Recherches Therapeutiques en Ophtalmologie de la Faculte de Medecine Necker, EA n°2502 du Ministere de la Recherche et de l'Enseignement Superieur, Universite Rene Descartes, Paris, and Unite INSERM 423, CHU Necker-Enfants Malades, Paris, France
&
Amina Berraho Laboratoire de Genetique et Biologie Moleculaire de la Faculte des Sciences, Universite IBN Tofail, Kenitra, and Departement d'Oto-Neuro-Ophtalmologie, Service d'Ophtalmologie B, Hopital des Specialites, Rabat, Morocco
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Pages 199-208 | Published online: 08 Jul 2009

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Ilaria Cosentino, Fabrizio Zeri, Peter G. Swann, Silvia Majore, Francesca Clementina Radio, Paolo Palumbo, Paola Grammatico & Vincenzo Petitti. (2016) Hyperferritinemia-cataract syndrome: Long-term ophthalmic observations in an Italian family. Ophthalmic Genetics 37:3, pages 318-322.
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Articles from other publishers (5)

Aidan B. Grosas & John A. Carver. 2021. Long‐lived Proteins in Human Aging and Disease. Long‐lived Proteins in Human Aging and Disease 59 96 .
Shan Li, Jianfei Zhang, Yixuan Cao, Yi You & Xiuli Zhao. (2019) Novel mutations identified in Chinese families with autosomal dominant congenital cataracts by targeted next-generation sequencing. BMC Medical Genetics 20:1.
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Alan S. Ma, John R. Grigg, Gladys Ho, Ivan Prokudin, Elizabeth Farnsworth, Katherine Holman, Anson Cheng, Frank A. Billson, Frank Martin, Clare Fraser, David Mowat, James Smith, John Christodoulou, Maree Flaherty, Bruce Bennetts & Robyn V. Jamieson. (2016) Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next‐Generation Sequencing. Human Mutation 37:4, pages 371-384.
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Venkata Pulla Rao Vendra, Ismail Khan, Sushil Chandani, Anbukkarasi Muniyandi & Dorairajan Balasubramanian. (2016) Gamma crystallins of the human eye lens. Biochimica et Biophysica Acta (BBA) - General Subjects 1860:1, pages 333-343.
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Arif O. Khan. (2012) Hereditary pediatric cataract on the Arabian Peninsula. Saudi Journal of Ophthalmology 26:1, pages 67-71.
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