Wiedemann H R
Department of Pediatrics, Christian-Albrechts-Universität, Kiel, Germany.
Am J Med Genet. 1997 Jan 20;68(2):222-4. doi: 10.1002/(sici)1096-8628(19970120)68:2<222::aid-ajmg20>3.0.co;2-v.
From personal observations, I review the genetic disorders of salivary gland development and function, including the lacrimo-auriculodentodigital (LADD) syndrome, autosomal dominant hypoplasia/agenesis of salivary and/or lacrimal glands, chronic recurrent sialadenitis, polycystic-dysgenetic disease of the parotids and salivary calculi.
通过个人观察,我回顾了唾液腺发育和功能的遗传性疾病,包括泪腺-耳-齿-指(LADD)综合征、常染色体显性遗传性唾液腺和/或泪腺发育不全/缺失、慢性复发性涎腺炎、腮腺多囊发育异常疾病和唾液腺结石。