Efficacy of Living Donor Liver Transplantation for Patients With Methylmalonic Acidemia

American Journal of Transplantation - Tập 7 Số 12 - Trang 2782-2787 - 2007
Daisuke Morioka1, Mureo Kasahara2, Reiko Horikawa3, Shinji Yokoyama2, Akinari Fukuda2, Atsuko Nakagawa4
1Department of Transplant Surgery, National Center for Child Health and Development, Tokyo, Japan
2Department of Transplant Surgery
3Department of Endocrinology and Metabolism
4Department of Pathology, National Center for Child Health and Development, Tokyo, Japan

Tóm tắt

Từ khóa


Tài liệu tham khảo

Saudubray JM, Charpentier C. Diagnosis/algorithms. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds). The Metabolic and Molecular Bases of Inherited Diseases, 8th Ed. New York: Mc Graw-Hill, Inc; 2001; 1327–1403

Kasahara, 2006, Current role of liver transplantation for methylmalonic acidemia: A review of the literature, Pediatr Transplant, 10, 943, 10.1111/j.1399-3046.2006.00585.x

Fenton WA, Rosenberg L. Disorders of propionate and methylmalonate metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D, Child B, Kinzler KW, Vogelstein B (eds). The Metabolic and Molecular Basics of Inherited Diseases. 8th Ed. New York: McGraw-Hill; 2001; 1423–1449.

Varogli, 2000, High cognitive outcome in an adolescent with mut- methylmalonic acidemia, Am J Med Genet, 96, 192, 10.1002/(SICI)1096-8628(20000403)96:2<192::AID-AJMG14>3.0.CO;2-J

Tanpaiboon, 2005, IEM digest: Methylmalonic acidemia, Mol Genet Metab, 85, 2, 10.1016/j.ymgme.2005.03.008

Nyhan, 2002, Progressive neurologic disability in methylmalonic acidemia despite transplantation of the liver, Eur J Pediatr, 161, 377, 10.1007/s00431-002-0970-4

Kaplan P, Mazur AM, Smith R et al. Transplantation for maple syrup urine disease (MSUD) and methylmalonic acidemia (MMA). J Inherit Metab Dis 1997; 20S: 37.

Nagarajan, 2005, Management of methylmalonic acidemia by combined liver-kidney transplantation, J Inherit Metab Dis, 28, 517, 10.1007/s10545-005-0517-8

Tanaka K, Inomata Y, Kaihara S, (eds). Living-Donor Liver Transplantation. Barcelona, Spain: Prous Science; 2003.

Kuczmarski, 2000, CDC Growth Charts: United States, Adv Data, 8, 1

Rutter, 1998, Developmental catch-up, and deficit, following adoption after severe global early privation, J Child Psychol Psychiatry, 39, 465, 10.1017/S0021963098002236

Morioka, 2005, Living donor liver transplantation for noncirrhotic inheritable metabolic liver diseases: Impact of the use of heterozygous donors, Transplantation, 80, 623, 10.1097/01.tp.0000167995.46778.72

Morioka, 2005, Living donor liver transplantation for pediatric patients with inheritable metabolic disorders, Am J Transplant, 5, 2754, 10.1111/j.1600-6143.2005.01084.x

Morioka, 2005, Current role of liver transplantation for the treatment of urea cycle disorders: A review of the worldwide English literature and 13 cases at Kyoto University, Liver Transpl, 11, 1332, 10.1002/lt.20587

Horster, 2004, Pathophysiology, diagnosis, and treatment of methylmalonic aciduria- recent advances and new challenges, Pediatr Nephrol, 19, 1071, 10.1007/s00467-004-1572-3

van’t Hoff W, McKiernan PJ, Surtees RA, Leonard JV. Liver transplantation for methylmalonic acidaemia. Eur J Pediatr 1999; S70–S74.