Brandrup F
Acta Derm Venereol. 1984;64(3):220-6.
Analysis of the presence of psoriasis in all first-degree relatives of psoriatic twin probands, 38 monozygotic (MZ) and 24 dizygotic (DZ), has been performed in order to clarify if genetic heterogeneity might be present (the twin-family method). The probands were derived from a population based sample of like-sexed twin pairs. An almost identical frequency of psoriasis in parents, siblings and children, with no sex difference, was found. By comparisons of empirical risk figures for psoriasis in first-degree relatives of concordant as compared with discordant MZ probands and HLA-B 13 and/or HLA-B 17 positive MZ probands compared with MZ probands lacking these antigens, no clue to the presence of genetic heterogeneity was found. An almost identical risk in co-twins and ordinary siblings of DZ-probands was found. The data were incompatible with autosomal recessive or X-linked inheritance, but not incompatible with autosomal dominant inheritance with reduced penetrance or with multifactorial inheritance.
为了明确是否可能存在遗传异质性(双生子家系法),对38对单卵双生子(MZ)和24对双卵双生子(DZ)银屑病先证者的所有一级亲属进行了银屑病患病情况分析。先证者来自基于人群的同性双生子对样本。研究发现,父母、兄弟姐妹和子女中银屑病的发病频率几乎相同,且无性别差异。通过比较同卵双生子先证者中一致与不一致的一级亲属患银屑病的经验风险数据,以及比较携带HLA - B13和/或HLA - B17的同卵双生子先证者与缺乏这些抗原的同卵双生子先证者,未发现存在遗传异质性的线索。双卵双生子先证者的同胞和普通兄弟姐妹的患病风险几乎相同。这些数据与常染色体隐性或X连锁遗传不相符,但与外显率降低的常染色体显性遗传或多因素遗传并不矛盾。