Hardikar syndrome: long term outcome of a rare genetic disorder
Nydegger, Andreas × Van Dyck, Maria Fisher, Robert A Jaeken, Jaak Hardikar, Winita #
American Journal of Medical Genetics A vol:146A issue:19 pages:2468-72
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.