Parotid Aplasia or Hypoplasia (Salivary Gland Absence; Lacrimal Puncta Absence)
General: Autosomal dominant.
Ocular: Lacrimal gland aplasia; absence or severe dysfunction of lacrimal glands.
Clinical: Aplasia of parotid salivary glands; hemifacial microsomia; mandibulofacial dysostoses; xerostomia; rampant caries; edentulous, salivary gland dysfunction; parotid agenesis or hypoplasia; impalpable parotid gland; absence of the orifice of Stensen duct; bilateral parotid gland aplasia.
McKusick VA. Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders, 12th ed. Baltimore: The Johns Hopkins University Press, 1998.
Online Mendelian Inheritance in Man, OMIM. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University and National Center for Biotechnology Information, National Library of Medicine, February 12, 2007. World Wide Web URL: https://www.ncbi.nlm.nih.gov/omim/.
Wiesenfeld D, et al. Familial parotid gland aplasia. J Oral Med 1985; 40:84-85.
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