Abstract

Background

Respiratory and gastrointestinal manifestations are the main causes of mortality and morbidity in cystic fibrosis. Although these symptoms are well recognized, ophthalmic involvement of cystic fibrosis secondary to vitamin A deficiency is uncommon and has been reported very rarely in the medical literature.

Case presentation

Here, we report a 2.5-year-old Iranian boy who presented with bilateral corneal xerosis and corneal opacity secondary to vitamin A deficiency related to cystic fibrosis malabsorption.

Conclusion

Malabsorption of fat-soluble vitamins is a common presentation in cystic fibrosis, but corneal opacity secondary to vitamin A deficiency as the initial presentation of cystic fibrosis is a very rare manifestation of fat malabsorption. This highlights the importance of complete systemic examination besides ophthalmic examination in approaching a child with ophthalmic complaint.

Details

Title
Corneal opacification, an atypical presentation of cystic fibrosis: a case report and review of the literature
Author
Farahbakhsh, Nazanin  VIAFID ORCID Logo  ; Bagherian, Neda; Shabanpourhaghighi, Sajad; Khalilzadeh, Soheila; Seyed Ahmad Tabatabaii; Khanbabaee, Ghamartaj
Pages
1-3
Section
Case report
Publication year
2022
Publication date
2022
Publisher
BioMed Central
e-ISSN
17521947
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2666691560
Copyright
© 2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.