Detalhes bibliográficos
| Autor(a) principal: |
Petroni,Roberta Cardoso |
| Data de Publicação: |
2017 |
| Outros Autores: |
Rosa,Susana Elaine Alves da,
Carvalho,Flavia Pereira de,
Santana,Rúbia Anita Ferraz,
Hyppolito,Joyce Esteves,
Nascimento,Claudia Mac Donald Bley,
Hamerschlak,Nelson,
Campregher,Paulo Vidal |
| Tipo de documento: |
Relatório
|
| Idioma: |
eng |
| Título da fonte: |
Einstein (São Paulo) |
| Texto Completo: |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082017000400492
|
Resumo: |
ABSTRACT Hereditary hyperferritinemia-cataract syndrome is an autosomal dominant genetic disorder associated with mutations in the 5’UTR region of the ferritin light chain gene. These mutations cause the ferritin levels to increase even in the absence of iron overload. Patients also develop bilateral cataract early due to accumulation of ferritin in the lens, and many are misdiagnosed as having hemochromatosis and thus not properly treated. The first cases were described in 1995 and several mutations have already been identified. However, this syndrome is still a poorly understood. We report two cases of unrelated Brazilian families with clinical suspicion of the syndrome, which were treated in our department. For the definitive diagnosis, the affected patients, their parents and siblings were submitted to Sanger sequencing of the 5’UTR region for detection of the ferritin light gene mutation. Single nucleotide polymorphism-like mutations were found in the affected patients, previously described. The test assisted in making the accurate diagnosis of the disease, and its description is important so that the test can be incorporated into clinical practice. |