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.