Myxomas, Spotty Pigmentation, and Endocrine Overactivity Syndrome (NAME Syndrome)
General: Autosomal dominant.
Ocular: Eyelid myxomas; pigmented lesions of the caruncle or conjunctival 343i82d semilunar fold.
Clinical: Cardiac, cutaneous, or mammary myxomas; acromegaly; adrenal, pituitary, and testicular neoplasms; Cushing syndrome; sexual precocity; spotty skin pigmentation.
Danoff A, et al. Adrenocortical micronodular dysplasia, cardiac myxomas, lentigines and spindle cell tumors: report of a kindred. Arch Intern Med 1987; 147:443.
Kennedy RH, et al. Ocular pigmented spots and eyelid myxomas. Am J Ophthalmol 1987; 104:533-538.
Koopman RJJ, et al. Autosomal dominant transmission of the NAME syndrome. Hum Genet 1991; 86:300-304.
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/.
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