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Ophthalmic Genetics Volume 37, 2016 - Issue 3
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Letters to the Journal

Regarding corneal decompensation in recessive cornea plana

Amani AlBakriDivision of Pediatric Ophthalmology, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia
&
Arif O. KhanEye Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab EmiratesCorrespondence[email protected]
Pages 350-351 | Published online: 08 Feb 2016

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Muralidhar Ramappa, Divya Sree Ramya Achanta, Ashik Mohamed & Sunita Chaurasia. (2020) Corneal endothelial alterations in Recessive Cornea Plana: a report of 4 patients and review of literature. Ophthalmic Genetics 41:6, pages 659-662.
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Arif O. Khan. (2018) Corneal ectasia in a boy with homozygous KERA mutation. Ophthalmic Genetics 39:1, pages 141-143.
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Articles from other publishers (2)

Chengzi Huang, Xigui Long, Can Peng, Pengsiyuan Lin, Hu Tan, Weigang Lv & Lingqian Wu. (2019) Novel variants in the KERA gene cause autosomal recessive cornea plana in a Chinese family: A case report. Molecular Medicine Reports.
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Lubica Dudakova, Jang Hee J. Vercruyssen, Irina Balikova, Lavina Postolache, Bart P. Leroy, Pavlina Skalicka & Petra Liskova. (2018) Analysis of KERA in four families with cornea plana identifies two novel mutations . Acta Ophthalmologica 96:1, pages e87-e91.
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