Ontology highlight
ABSTRACT:
SUBMITTER: Giordano P
PROVIDER: S-EPMC3917534 | biostudies-other | 2014 Jan
REPOSITORIES: biostudies-other
Giordano Paola P Lassandro Giuseppe G Sangerardi Maria M Faienza Maria Felicia MF Valente Federica F Martire Baldassarre B
Italian journal of pediatrics 20140125
Kabuki syndrome (also called Niikawa-Kuroki syndrome) is a rare genetic disease described for the first time in Japan, characterised by anomalies in multiple organ systems and often associated with autoimmune disorders and impaired immune response. We herein report the clinical history, the therapeutic approach and the outcome of two children with Kabuki syndrome who developed autoimmune haematological disorders (haemolytic anaemia and immune thrombocytopenia). Factors regarding differential dia ...[more]