How to cite this article: Nydegger A, Van Dyck M, Fisher RA, Jaeken J, Hardikar W. 2008. Hardikar syndrome: Long term outcome of a rare genetic disorder. Am J Med Genet Part A 146A:2468–2472.
Hardikar syndrome: Long term outcome of a rare genetic disorder†
Article first published online: 17 MAR 2008
Copyright © 2008 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 146A, Issue 19, pages 2468–2472, 1 October 2008
How to Cite
Nydegger, A., Van Dyck, M., Fisher, R. A., Jaeken, J. and Hardikar, W. (2008), Hardikar syndrome: Long term outcome of a rare genetic disorder. Am. J. Med. Genet., 146A: 2468–2472. doi: 10.1002/ajmg.a.32226
- Issue published online: 22 SEP 2008
- Article first published online: 17 MAR 2008
- Manuscript Accepted: 3 DEC 2007
- Manuscript Received: 22 SEP 2007
- cleft lip;
- liver transplantation;
- pigmentary retinopathy;
- vesico-ureteral reflux
Hardikar syndrome is a rare disorder of unknown etiology. Features of the syndrome are manifold with a predominance of liver and renal involvement. The syndrome is clearly distinct from other previously described syndromes such as Alagille syndrome, congenital hepatic fibrosis, Caroli disease, and Kabuki make-up syndrome. To date, only four cases of Hardikar syndrome have been published worldwide. We report here on the long term outcome of these patients. © 2008 Wiley-Liss, Inc.