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...
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| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Ordem dos Médicos
2025-03-01
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| Series: | Acta Médica Portuguesa |
| Subjects: | |
| Online Access: | https://actamedicaportuguesa.com/revista/index.php/amp/article/view/22524 |
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