Agarwal S S, Lahori U C, Mehta S K, Smith D G, Bajpai P C
Hum Hered. 1979;29(2):82-9. doi: 10.1159/000153021.
Detailed pedigree charts were prepared from 120 index patients suffering from Indian childhood cirrhosis (ICC). Of the 120 families, 84 were informative for segregation analysis. Since families were ascertained through patients who came to hospital for treatment, the data were analyzed according to a single-selection model. The observed segregation ratio for the entire data was significantly lower than the one expected under the hypothesis of autosomal recessive inheritance (p = smaller than 0.005). On the other hand, the segregation data for families with at least two affected children (multiplex families) were compatible with autosomal recessive inheritance. On this basis, however, at least 50% of all the cases of ICC would have to be of nongenetic origin. Alternatively, analysis of the data by the Falconer method indicated that ICC could be of multifactorial origin with very strong genetic determination (over 85%).
为120例患有印度儿童肝硬化(ICC)的索引患者绘制了详细的系谱图。在这120个家庭中,有84个家庭可用于分离分析。由于这些家庭是通过前来医院治疗的患者确定的,因此数据是根据单选择模型进行分析的。整个数据的观察到的分离比显著低于常染色体隐性遗传假设下预期的分离比(p小于0.005)。另一方面,至少有两个患病子女的家庭(多重家庭)的分离数据与常染色体隐性遗传相符。然而,在此基础上,所有ICC病例中至少50%必须是非遗传起源的。或者,通过Falconer方法对数据进行分析表明,ICC可能是多因素起源,具有很强的遗传决定性(超过85%)。