Zlotogora J, Sagi M, Cohen T
Department of Human Genetics, Hadassah Medical Center, Hebrew University, Jerusalem, Israel.
Am J Med Genet. 1994 Jan 15;49(2):202-4. doi: 10.1002/ajmg.1320490208.
Fourteen families in which more than one child was diagnosed with hydrocephalus of prenatal onset were seen in our genetic counseling clinic. In 7 families only males were affected: in 2 X-linked hydrocephalus was diagnosed while X-linked inheritance was suspected in 3 other families. These 5 families were of Jewish origin. In the 8 families of Arab origin, the parents of the affected children were consanguineous. In 6 of these families at least one female was affected and the hydrocephalus was most probably inherited as an autosomal recessive trait. This type of hydrocephalus of prenatal onset appears to be frequent among Palestinian Arabs.
我们的遗传咨询门诊接待了14个家庭,这些家庭中不止一个孩子被诊断为产前脑积水。在7个家庭中,只有男性患病:其中2个家庭被诊断为X连锁脑积水,另外3个家庭怀疑为X连锁遗传。这5个家庭是犹太裔。在8个阿拉伯裔家庭中,患病孩子的父母是近亲。在其中6个家庭中,至少有一名女性患病,脑积水很可能是作为常染色体隐性性状遗传的。这种产前脑积水在巴勒斯坦阿拉伯人中似乎很常见。