Gedschold J, Szibor R, Kropf S, Berger M
Abteilung Humangenetik, Medizinische Akademie Magdeburg, German Democratic Republic.
Hum Genet. 1988 Dec;80(4):399-400. doi: 10.1007/BF00273662.
When 458 parents of children suffering from cystic fibrosis (CF) from all over the German Democratic Republic were interviewed to determine the number of their siblings, it was found that the maternal families had a total of 1369 children and the paternal, 1220. While the fathers of CF patients tended to originate from families with one or two children, more mothers than fathers came from families with three to twelve children (P = 0.01). The average number of children in the maternal families was 2.99; in the paternal families, only 2.66. To rule out any methodological errors, sibs of mothers and fathers of various control groups were studied. We found that the number of siblings in these groups was balanced. The differences in our findings are probably due to CF heterozygosity. The underlying mechanism is unknown.
当对来自德意志民主共和国各地的458名患有囊性纤维化(CF)儿童的父母进行访谈,以确定他们的兄弟姐妹数量时,发现母亲一方的家庭共有1369个孩子,父亲一方有1220个孩子。虽然囊性纤维化患者的父亲往往来自有一两个孩子的家庭,但来自有三到十二个孩子家庭的母亲比父亲更多(P = 0.01)。母亲一方家庭的孩子平均数量为2.99个;父亲一方家庭中仅为2.66个。为排除任何方法学上的错误,对各个对照组母亲和父亲的兄弟姐妹进行了研究。我们发现这些组中的兄弟姐妹数量是均衡的。我们研究结果中的差异可能是由于囊性纤维化杂合性。其潜在机制尚不清楚。