Stasiowska B, Sartoris S, Goitre M, Benso L
Arch Dis Child. 1981 Oct;56(10):793-5. doi: 10.1136/adc.56.10.793.
We report a mother and daughter with Rapp-Hodgkin ectodermal dysplasia syndrome. Features of the previously described cases were confirmed, although no growth deficiencies were observed. Autosomal dominant inheritance was probable although X-linked transmission could not be excluded.
我们报告了一对患有拉普-霍奇金外胚层发育不良综合征的母女。尽管未观察到生长发育缺陷，但之前描述病例的特征得到了证实。虽然不能排除X连锁遗传，但很可能是常染色体显性遗传。
