Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare hematologic disease characterized by the transfer of maternal alloantibodies against red blood cell antigens of the Kell family to a fetus positive for this antigen across the placental barrier, causing suppression of erythropoiesis with reticulocytopenia and anemia, as well as alloimmune hemolysis. Severe anemia may lead to hydrops fetalis. Significant hyperbilirubinemia is rare in this condition. Disease data Klasyfikacja Disease Synonimy Anti-K HDN Matczyna alloimmunizacja anty-Kell Maternal anti-Kell alloimmunization Kod ORPHA 275944 Kod OMIM - Kod ICD10 P55.8 Kod ICD11 - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl