{Reference Type}: Case Reports
{Title}: [A case report of secondary hemochromatosis caused by a mutation in the ETV6 gene].
{Author}: Zhang XL;Weng YH;Yang YF;
{Journal}: Zhonghua Gan Zang Bing Za Zhi
{Volume}: 31
{Issue}: 9
{Year}: 2023 Sep 20
暂无{DOI}: 10.3760/cma.j.cn501113-20230112-00021
{Abstract}: 血色病常分为原发性及继发性，临床以继发性血色病较为常见，且临床症状多不典型，易引起误诊误治。现介绍1例以肝功能异常及3系减少就诊的继发性血色病患者，全外显子检测提示ETV6基因变异，以期启示临床，找准病因，及时干预，改善患者预后。.