Literature DB >> 30536852

Heart transplantation in two adolescents with Danon disease.

Daniel Oren1, Peter Chau2, Melanie Manning3, Joann Kwong4, Beth D Kaufman5, Katsuhide Maeda6, David N Rosenthal5, Seth A Hollander5.   

Abstract

Danon disease (DD) is an X-linked dominant disorder caused by a mutation in the lysosomal-associated membrane protein-2 (LAMP-2) gene coding for the LAMP-2 protein. We report two cases of successful heart transplantation (HT) in adolescent brothers with DD, including one who was bridged to HT for 34 days with a HeartWare left ventricular assist device. In both patients, the post-transplant course was complicated by profound skeletal muscle weakness that resolved with corticosteroid withdrawal. These cases highlight that both HT and ventricular assist device support are feasible in patients with DD. Corticosteroid use may exacerbate skeletal myopathy, and therefore, steroid minimization may be warranted whenever possible.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  adolescents; cardiac function; cardiomyopathy; pediatric heart transplant; steroid discontinuation; steroid-free immunosuppression

Mesh:

Year:  2018        PMID: 30536852     DOI: 10.1111/petr.13335

Source DB:  PubMed          Journal:  Pediatr Transplant        ISSN: 1397-3142


  1 in total

1.  Three female patients with Danon disease presenting with predominant cardiac phenotype: a case series.

Authors:  Bart A Mulder; Yvonne M Hoedemaekers; Maarten P van den Berg; Rosa L E van Loon; Anna M Wind; Jan D H Jongbloed; Ans C P Wiesfeld
Journal:  Eur Heart J Case Rep       Date:  2019-07-29
  1 in total

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