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Brain abnormalities in fucosidosis: transplantation or supportive therapy?
Jiang, Minyan; Liu, Sha; Jiang, Hua; Lin, Yunting; Shao, Yongxian; Hu, Hao; Zhao, Xiaoyuan; Liu, Hongsheng; Huang, Yonglan; Liu, Li.
Afiliação
  • Jiang M; Department of Pediatric Endocrinology and Genetic Metabolism, Guangzhou Women and Children's Medical Center, Guangzhou, China.
  • Liu S; Department of Pediatric Hematology, Guangzhou Women and Children's Medical Center, Guangzhou, China.
  • Jiang H; Department of Pediatric Hematology, Guangzhou Women and Children's Medical Center, Guangzhou, China.
  • Lin Y; Department of Pediatric Endocrinology and Genetic Metabolism, Guangzhou Women and Children's Medical Center, Guangzhou, China.
  • Shao Y; Department of Pediatric Endocrinology and Genetic Metabolism, Guangzhou Women and Children's Medical Center, Guangzhou, China.
  • Hu H; Department of Pediatric Endocrinology and Genetic Metabolism, Guangzhou Women and Children's Medical Center, Guangzhou, China.
  • Zhao X; Department of Pediatric Endocrinology and Genetic Metabolism, Guangzhou Women and Children's Medical Center, Guangzhou, China.
  • Liu H; Medical Imaging Department, Guangzhou Women and Children's Medical Center, Guangzhou, China.
  • Huang Y; Department of Pediatric Endocrinology and Genetic Metabolism, Guangzhou Women and Children's Medical Center, Guangzhou, China. xxhuang321@163.com.
  • Liu L; Department of Pediatric Endocrinology and Genetic Metabolism, Guangzhou Women and Children's Medical Center, Guangzhou, China. liliuchina@qq.com.
Metab Brain Dis ; 32(2): 317-320, 2017 04.
Article em En | MEDLINE | ID: mdl-28238202
Fucosidosis is a rare lysosomal storage disease caused by α-fucosidase deficiency, which leads to progressive neurological deterioration and death. Hematopoietic stem cell transplantation is the best curative therapy if performed during the early stages of disease. We report two fucosidosis patients with brain abnormalities and the challenge faced in their management. The first patient received supportive therapy and the second one firstly underwent unrelated donor umbilical cord blood transplantation. After a period of follow-up, we found neurological symptoms were worsening day by day on patient1. By contrast, patient2 who received cord blood transplantation acquired clinical neurologic improvement in response to normalization of deficient enzymatic activity. This report indicates that hematopoietic transplant could reduce the severity and retard the progression of clinical neurological deterioration. Umbilical cord blood transplantation is a novel approach for treating fucosidosis patients who lack suitable bone morrow donors.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Transplante de Células-Tronco Hematopoéticas / Transplante de Células-Tronco de Sangue do Cordão Umbilical / Fucosidose Tipo de estudo: Etiology_studies Limite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Metab Brain Dis Assunto da revista: CEREBRO / METABOLISMO Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Transplante de Células-Tronco Hematopoéticas / Transplante de Células-Tronco de Sangue do Cordão Umbilical / Fucosidose Tipo de estudo: Etiology_studies Limite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Metab Brain Dis Assunto da revista: CEREBRO / METABOLISMO Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos