van der Burgt I, Haraldsson A, Oosterwijk J C, van Essen A J, Weemaes C, Hamel B
Department of Human Genetics, University Hospital Nijmegen, The Netherlands.
Am J Med Genet. 1991 Dec 1;41(3):371-80. doi: 10.1002/ajmg.1320410320.
We describe 7 cases of cartilage hair hypoplasia (CHH) with emphasis on the clinical and immunological aspects. The literature on CHH is reviewed and symptoms in 63 non-Amish cases are summarized. In this autosomal recessive disorder the immunodeficiency, hair abnormalities, and severity of skeletal involvement show extremely variable expressivity, between and within families. Two of the 3 sib-pairs among our cases demonstrate the great difference in expression within one family. At adult age roentgenological abnormalities can be very mild, or even absent. An impairment in cell-mediated immunity is present in all of our cases and seems a consistent manifestation in CHH; however, sometimes it is very subtle and without clinical symptoms.
我们描述了7例软骨毛发发育不全(CHH)病例,重点关注临床和免疫学方面。对CHH的文献进行了综述,并总结了63例非阿米什病例的症状。在这种常染色体隐性疾病中,免疫缺陷、毛发异常和骨骼受累的严重程度在不同家庭之间以及家庭内部表现出极大的变异性。我们病例中的3对同胞中有2对显示出一个家庭内部表达的巨大差异。在成年期,放射学异常可能非常轻微,甚至不存在。我们所有病例均存在细胞介导免疫功能受损,这似乎是CHH的一个一致表现;然而,有时它非常隐匿且无临床症状。