Lebovitz R M, Pauli R M, Laxova R
Am J Dis Child. 1984 Jun;138(6):571-3. doi: 10.1001/archpedi.1984.02140440055014.
Medical records of all patients with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency who were followed up at the University of Wisconsin Hospitals, Madison, from 1956 to 1979, were reviewed to document the ages at diagnoses. Without newborn screening, the average age at diagnosis for 32 patients was 12.6 months (7.3 months for female infants and children and 22.7 months for male infants and children). In the newborn population, ambiguity was recognized in 15 of 21 female infants and in none of the male infants. Initial-appearing symptoms in female infants and children included ambiguous genitalia in 15 of 21, precocious puberty in four, and salt-losing crises in two. In the male infants and children, the reasons for diagnoses were salt-losing crises in seven of 11 and precocious puberty in four. These results indicate that in the absence of newborn screening, diagnosis is frequently delayed.
对1956年至1979年在麦迪逊市威斯康星大学医院接受随访的所有因21 - 羟化酶缺乏导致先天性肾上腺皮质增生症患者的病历进行了回顾,以记录诊断年龄。在没有新生儿筛查的情况下,32例患者的平均诊断年龄为12.6个月(女婴和女童为7.3个月,男婴和男童为22.7个月)。在新生儿群体中,21例女婴中有15例存在生殖器模糊,男婴中无一例出现这种情况。女婴和女童最初出现的症状包括21例中有15例生殖器模糊、4例性早熟和2例失盐危象。在男婴和男童中,诊断原因是11例中有7例失盐危象和4例性早熟。这些结果表明,在没有新生儿筛查的情况下,诊断常常延迟。