Hyperferritinemia-cataract syndrome: Long-term ophthalmic observations in an Italian family-Reference-Cited by-同舟云学术

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Hyperferritinemia-cataract syndrome: Long-term ophthalmic observations in an Italian family

Published:2016-02-05 Issue:3 Volume:37 Page:318-322
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Cosentino Ilaria¹,Zeri Fabrizio²,Swann Peter G.³⁴,Majore Silvia¹,Radio Francesca Clementina¹,Palumbo Paolo²⁵,Grammatico Paola¹,Petitti Vincenzo⁶

Affiliation:

1. Medical Genetics, Molecular Medicine Department, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy

2. Department of Sciences, Roma Tre University, Rome, Italy

3. School of Optometry, Hong Kong Polytechnic University, Hong Kong

4. School of Optometry and Vision Science, Queensland University of Technology, Brisbane, Australia

5. Unit of Ophthalmology, “G.B.Grassi” Hospital, Rome, Italy

6. Department of Ophthalmology, San Camillo-Forlanini Hospital, Rome, Italy

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.3109/13816810.2015.1059460

Reference28 articles.

1. A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract

2. Bilateral cataract and high serum ferritin: a new dominant genetic disorder?

3. Hereditary Hyperferritinemia-Cataract Syndrome

4. Hyperferritinaemia-cataract syndrome: Worldwide mutations and phenotype of an increasingly diagnosed genetic disorder

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1. Four mutations identified in Chinese families with autosomal dominant congenital cataracts by next-generation sequencing;Genes & Genomics;2024-06-13

2. Un'insolita associazione: iperferritinemia e cataratta;Medico e Bambino Pagine elettroniche;2023-12-22

3. Hyperferritinemia and non-HFE hemochromatosis: differential diagnosis and workup;Acta Gastro Enterologica Belgica;2023-06

4. Cataract;Clinical Ophthalmic Genetics and Genomics;2022

5. Ferritin L-subunit gene mutation and hereditary hyperferritinaemia cataract syndrome (HHCS): a case report and literature review;Hematology;2021-01-01

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