Unna II Syndrome (Marie-Unna Syndrome)
General: Both sexes affected; rare; autosomal dominant; onset in children.
Ocular: Eyebrows and eyelashes missing.
Clinical: Loss of hair; scant growth of axillary and pubic hair, teeth, and nails; loss of hair in the eyebrows, eyelashes, and body.
Magalini SI, Scrascia E. Dictionary of Medical Syndromes, 2nd ed. Philadelphia: JB Lippincott, 1981.
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/.
Unna M. Ueber Hypotricosis congenita hereditaria. Dermatol Wochenschr 1925; 81:1167-l178.
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