Penchaszadeh V B, Coco R
J Med Genet. 1975 Jun;12(2):193-9. doi: 10.1136/jmg.12.2.193.
Two unrelated children, not affected with Down's syndrome, with strikingly similar phenotypes and an extra G-like chromosome are presented. Quinacrine and trypsin-Giemsa banding identified the extra chromosome as No. 22. The phenotype of these patients and the review of 15 additional similar cases from the literature permit a definition of the cardinal features of trisomy 22; mental and growth retardation, microcephaly and craniofacial asymmetry, strabismus, beaked and prominent nose, long philtrum, cleft palate, micrognathia, large low set ears with preauricular tags and/or pits, long slender fingers, congenital heart disease, inguinal hernia, and hip dislocation.
本文报告了两名无亲缘关系且未患唐氏综合征的儿童,他们具有极其相似的表型,并带有一条额外的类G染色体。喹吖因和胰蛋白酶 - 吉姆萨显带技术确定这条额外的染色体为22号染色体。根据这些患者的表型以及对文献中另外15例类似病例的回顾,我们可以明确22三体综合征的主要特征:智力和生长发育迟缓、小头畸形和颅面不对称、斜视、喙状且突出的鼻子、长人中、腭裂、小颌畸形、低位大耳并伴有耳前赘生物和/或耳前凹、手指细长、先天性心脏病、腹股沟疝以及髋关节脱位。