Levene C, Rudolphson Y, Shechter Y
Transfusion. 1980 Nov-Dec;20(6):714-5. doi: 10.1046/j.1537-2995.1980.20681057162.x.
A second case of hemolytic disease of the newborn caused by Jsa sensitization is reported. The child was mildly affected and transfusions were not required. The mother and father are Arabs. Jsa was present in the father, the baby in question, and a sibling. In addition, the Fy gene was present in both mother and father, and in two of their three children.
报道了第二例因Jsa致敏引起的新生儿溶血病病例。该患儿症状较轻，无需输血。患儿父母为阿拉伯人。父亲、患儿及其一个兄弟姐妹均存在Jsa。此外，母亲和父亲及其三个孩子中的两个携带Fy基因。
