Hirschhorn R, Beratis N, Rosen F S, Parkman R, Stern R, Polmar S
Lancet. 1975 Jan 11;1(7898):73-5. doi: 10.1016/s0140-6736(75)91075-2.
Deficiency of red-blood-cell adenosine deaminase (R.B.C.-A.D.A.) has been reported in a proportion of patients with the autosomal recessive form of severe combined immunodeficiency (S.C.I.D.). In a family in which a child had died with S.C.I.D., R.B.C.-A.D.A. levels in the parents and other members of the family were compatible with a heterozygous state for A.D.A. deficiency. Cultured amniotic-fluid cells obtained from a subsequent pregnancy contained less than 1.5% of A.D.A. activity of normal amniotic cultures. The prenatal diagnosis of A.D.A. deficiency was confirmed at birth by the absence of A.D.A. ACTIVITY IN THE CHILD'S RED-BLOOD-CELLS. Clinical and laboratory findings in this child are similar to those of the sibling who had died with S.C.I.D.
据报道,部分患有常染色体隐性重症联合免疫缺陷病(S.C.I.D.)的患者存在红细胞腺苷脱氨酶(R.B.C.-A.D.A.)缺乏的情况。在一个孩子死于S.C.I.D.的家庭中,父母及其他家庭成员的R.B.C.-A.D.A.水平与腺苷脱氨酶缺乏的杂合状态相符。从随后一次怀孕中获取的羊水培养细胞所含的腺苷脱氨酶活性不到正常羊水培养物的1.5%。该孩子出生时红细胞中缺乏腺苷脱氨酶活性,从而证实了腺苷脱氨酶缺乏的产前诊断。这个孩子的临床和实验室检查结果与死于S.C.I.D.的同胞相似。