A de novo ANK1 mutation associated to hereditary spherocytosis: a case report

• Main Authors: Ti-Long Huang (Author), Bao-Hua Sang (Author), Qing-Ling Lei (Author), Chun-Yan Song (Author), Yun-Bi Lin (Author), Yu Lv (Author), Chun-Hui Yang (Author), Na Li (Author), Yue-Huang Yang (Author), Xian-Wen Zhang (Author), Xin Tian (Author)
• Format: Book
• Published: BMC, 2019-02-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background Hereditary spherocytosis (HS) is a type of hemolytic anemia caused by abnormal red cell membrane skeletal proteins with few unique clinical manifestations in the neonate and infant. An ANK1 gene mutation is the most common cause of HS. Case presentation The patient was a 11-month...