Wilkie A O, Campbell F M, Daubeney P, Grant D B, Daniels R J, Mullarkey M, Affara N A, Fitchett M, Huson S M
Department of Paediatric Genetics and Fetal Medicine, Hospitals for Sick Children, London, United Kingdom.
Am J Med Genet. 1993 Jun 15;46(5):597-600. doi: 10.1002/ajmg.1320460527.
We describe 2 karyotypically male infants with terminal deletion of 10q and mental retardation, multiple phenotypic anomalies and abnormal genitalia. One [karyotype 46,XY, del(10)(q26.1)] had female external genitalia; the other [karyotype 46,XY,-10,+der(10)t (10;16)(q26.2;q21)] had an intersex phenotype. Of 8 males previously reported with terminal 10q deletion as the major or only cytogenetic abnormality, 2 had an intersex phenotype, and the others all had combinations of cryptorchidism, micropenis, and hypospadias. Terminal 10q deletions appear to be strongly associated with abnormal male genital development, and should be specifically searched for in the cytogenetic workup of such cases.
我们描述了2例核型为男性的婴儿,他们存在10号染色体长臂末端缺失,并伴有智力发育迟缓、多种表型异常及生殖器畸形。其中1例[核型为46,XY, del(10)(q26.1)]具有女性外生殖器;另1例[核型为46,XY,-10,+der(10)t (10;16)(q26.2;q21)]具有两性畸形表型。在先前报道的8例以10号染色体长臂末端缺失作为主要或唯一细胞遗传学异常的男性患者中,2例具有两性畸形表型,其他患者均合并有隐睾、小阴茎和尿道下裂。10号染色体长臂末端缺失似乎与男性生殖器发育异常密切相关,并应在这类病例的细胞遗传学检查中进行专门排查。