Síndrome hereditária hiperferritinemia-catarata: caso clínico
Hereditary hyperferritinemia-cataract syndrome is an autosomal dominant genetic disorder that is characterized by high serum ferritin levels without iron overload and early-onset cataracts. The authors describe the case of a 26-year-old woman with hyperferritinemia (1153.3 ng/mL, reference range 11.0 - 306.8 ng/mL), with no other abnormalities in iron metabolism, associated with cataracts diagnosed at the age of three. The diagnosis was confirmed by genetic testing with detection of a heterozygous variant in the FTL gene (c.-168G>T). It is important to recognise hereditary hyperferritinemia-cataract syndrome to avoid unnecessary medical procedures.
Authors
- Cláudia Diogo
- Sonia Sánchez Campos (ORCID: https://orcid.org/0009-0009-2443-7577)
- C.N. Fernandes (ORCID: https://orcid.org/0000-0001-5841-7800)
- Cristiana Vanessa Malhó
- Filipa Alçada
Institutions
- Instituto Politécnico de Leiria (PT)
- Administração Regional de Saúde de Lisboa e Vale do Tejo (PT)
Publication Details
- Journal
- Acta Médica Portuguesa
- Published
- 2025-03-14
- DOI
- https://doi.org/10.20344/amp.22524
- Primary Topic
- Iron Metabolism and Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00