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Publisher : instituto de ensino e pesquisa albert einstein

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Brazilian family with hyperferritinemia-cataract syndrome: case report.

Authors : Alvarenga AM; Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, SP, Brazil.; Silva NKD

Subjects: Hemochromatosis*/Hemochromatosis*/Hemochromatosis*/genetics ; Cataract*/Cataract*/Cataract*/diagnosis ; Cataract*/Cataract*/Cataract*/geneticsHyperferritinemia, hereditary, with congenital cataracts

Source: Einstein (Sao Paulo, Brazil) [Einstein (Sao Paulo)] 2022 Oct 24; Vol. 20, pp. eRC0076. Date of Electronic Publication: 2022 Oct 24 (Print Publication: 2022).Publisher: Instituto de Ensino e Pesquisa Albert Einstein Country of Publication: Brazil NLM ID: 101281800 Publication Model:

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Ferritin light chain gene mutations in two Brazilian families with hereditary hyperferritinemia-cataract syndrome.

Authors : Petroni RC; Hospital Israelita Albert Einstein, São Paulo, SP, Brazil.; Rosa SEAD

Subjects: Apoferritins/Apoferritins/Apoferritins/*blood ; Cataract/Cataract/Cataract/*congenital ; Iron/Iron/Iron/*blood Hyperferritinemia, hereditary, with congenital cataracts

Source: Einstein (Sao Paulo, Brazil) [Einstein (Sao Paulo)] 2017 Oct-Dec; Vol. 15 (4), pp. 492-495. Date of Electronic Publication: 2017 Jul 24.Publisher: Instituto de Ensino e Pesquisa Albert Einstein Country of Publication: Brazil NLM ID: 101281800 Publication Model:

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