Merlob P, Reisner S H, Zaizov R
Department of Neonatology, Beilinson Medical Center, Petah Tiqva, Israel.
Pediatr Hematol Oncol. 1986;3(2):175-8. doi: 10.3109/08880018609031214.
Two infants with hemolytic disease of the newborn due to Kell incompatibility are described. The peripheral blood smears revealed many spherocytes. This important hematologic sign in a neonate suggests not only ABO incompatibility, hereditary spherocytosis, or G6PD deficiency, but also the possibility of Kell incompatibility.
本文描述了两名因凯尔血型不合导致新生儿溶血病的婴儿。外周血涂片显示有许多球形红细胞。新生儿出现这一重要的血液学体征不仅提示ABO血型不合、遗传性球形红细胞增多症或葡萄糖-6-磷酸脱氢酶(G6PD)缺乏,还提示凯尔血型不合的可能性。