Literature DB >> 22405037

Liver transplantation followed by allogeneic hematopoietic stem cell transplantation for atypical mevalonic aciduria.

S Chaudhury1, L Hormaza, S Mohammad, J Lokar, U Ekong, E M Alonso, M S Wainwright, M Kletzel, P F Whitington.   

Abstract

Mevalonic aciduria because of mutations of the gene for mevalonate kinase causes limited synthesis of isoprenoids, the effects of which are widespread. The outcome for affected children is poor. A child with severe multisystem manifestations underwent orthotopic liver transplantation at age 50 months for the indication of end-stage liver disease. This procedure corrected liver function and eliminated portal hypertension, and the patient showed substantial improvement in neurological function. However, autoinflammatory episodes continued unabated until hematopoietic stem cell transplantation was performed at 80 months. Through this complex therapy, the patient now enjoys a high quality of life without significant disability. © Copyright 2012 The American Society of Transplantation and the American Society of Transplant Surgeons.

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Year:  2012        PMID: 22405037     DOI: 10.1111/j.1600-6143.2011.03989.x

Source DB:  PubMed          Journal:  Am J Transplant        ISSN: 1600-6135            Impact factor:   8.086


  16 in total

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Authors:  Erdal Sag; Yelda Bilginer; Seza Ozen
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Review 2.  Monogenic Periodic Fever Syndromes: Treatment Options for the Pediatric Patient.

Authors:  Seza Ozen; Selcan Demir
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Review 3.  To Extinguish the Fire from Outside the Cell or to Shutdown the Gas Valve Inside? Novel Trends in Anti-Inflammatory Therapies.

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4.  11-Month-Old Infant With Periodic Fevers, Recurrent Liver Dysfunction, and Perforin Gene Polymorphism.

Authors:  Grant S Schulert; Kevin Bove; Richard McMasters; Kathleen Campbell; Nancy Leslie; Alexei A Grom
Journal:  Arthritis Care Res (Hoboken)       Date:  2015-08       Impact factor: 4.794

Review 5.  Treatment of Smith-Lemli-Opitz syndrome and other sterol disorders.

Authors:  Melissa D Svoboda; Jill M Christie; Yasemen Eroglu; Kurt A Freeman; Robert D Steiner
Journal:  Am J Med Genet C Semin Med Genet       Date:  2012-10-05       Impact factor: 3.908

Review 6.  Inborn errors of metabolism underlying primary immunodeficiencies.

Authors:  Nima Parvaneh; Pierre Quartier; Parastoo Rostami; Jean-Laurent Casanova; Pascale de Lonlay
Journal:  J Clin Immunol       Date:  2014-08-01       Impact factor: 8.317

7.  Hematopoietic Cell Transplantation Ameliorates Autoinflammation in A20 Haploinsufficiency.

Authors:  Mayuka Shiraki; Eleri Williams; Norifumi Yokoyama; Kunihiro Shinoda; Zohreh Nademi; Kana Matsumoto; Hiroshi Nihira; Yoshitaka Honda; Kazushi Izawa; Ryuta Nishikomori; Mary A Slatter; Andrew J Cant; Andrew R Gennery; Hidenori Ohnishi; Hirokazu Kanegane
Journal:  J Clin Immunol       Date:  2021-08-24       Impact factor: 8.317

Review 8.  Hyper-IgD syndrome/mevalonate kinase deficiency: what is new?

Authors:  C M Mulders-Manders; A Simon
Journal:  Semin Immunopathol       Date:  2015-05-20       Impact factor: 9.623

Review 9.  Natural history of mevalonate kinase deficiency: a literature review.

Authors:  Shumin Zhang
Journal:  Pediatr Rheumatol Online J       Date:  2016-05-04       Impact factor: 3.054

Review 10.  Mevalonate kinase deficiency: current perspectives.

Authors:  Leslie A Favier; Grant S Schulert
Journal:  Appl Clin Genet       Date:  2016-07-20
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