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Case Reports

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

, , , , , , & show all
Pages 318-322 | Received 26 Apr 2015, Accepted 14 May 2015, Published online: 05 Feb 2016
 

ABSTRACT

Background: Hyperferritinemia-cataract syndrome (HCS) is a rare Mendelian condition characterized by bilateral cataract and high levels of serum ferritin in the absence of iron overload.

Methods: HCS was diagnosed in three adult siblings. In two of them it was possible to assess lens changes initially in 1995 and again in 2013. Serum ferritin, iron, transferrin concentrations and transferrin saturation percentage were also measured, and the Iron Responsive Element (IRE) region of the L-ferritin gene (FTL) was studied.

Results: Serum ferritin concentrations were considerably elevated while serum iron, transferrin and transferrin saturation levels were within the normal range in each sibling. Cataract changes in our patients were consistent with those previously reported in the literature. Progression of the cataract, an aspect of few studies in this syndrome, appeared to be quite limited in extent. The heterozygous +32G to T (-168G>T) substitution in the IRE of the FTL gene was detected in this family.

Conclusions: Ophthalmic and biochemical studies together with genetic testing confirmed HCS in three family members. Although the disorder has been extensively described in recent years, little is known regarding cataract evolution over time. In our cases, lens evaluations encompassed many years, identified bilateral cataract of typical morphology and supported the hypothesis that this unique clinical feature of the disease tends to be slowly progressive in nature, at least in adults.

Acknowledgment

is published with kind permission of the Editor of Contact Lens and Anterior Eye. It was the first-prize-winning photograph of the British Contact Lens Association Conference photography competition for 2013.

Declaration of interest

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.

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