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Myxomas, spotty pigmentation, and endocrine overactivity syndrome (name syndrome)


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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