Title of article :
Epstein syndrome with rapid progression to end stage renal disease
Author/Authors :
Alhindawi, Esam King Hussein Medical Center - Pediatric Department, Jordan , Al-Jbour, Samah King Hussein Medical Center - Pediatric Department, Jordan
Abstract :
The association of haematological abnormalities and hereditary nephritis is rare; it is mainly included in a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly, Fechtner, Sebastian, Epstein and Alport syndrome with macro thrombocytopenia. We are presenting a missed case of a boy who presented with epistaxis and his diagnostic work up revealed macrothrombocytopenia, sensorineural hearing loss and chronic nephropathy which constitute the Epstein syndrome, with rapid deterioration of kidney function.
Journal title :
Saudi Journal of Kidney Diseases and Transplantation
Journal title :
Saudi Journal of Kidney Diseases and Transplantation