Gillum-Anderson Syndrome 242h77c 242h77c 242h77c 242h77c 242h77c
General: Genetic defect responsible for weakness in the orbital connective tissue; proposed connective tissue defect of sclera, zonules, and levator aponeurosis.
Ocular: Dislocated lenses; high myopia; bilateral ptosis typical for levator disinsertions; ectopia lentis.
Gillum WN, Anderson RL. Dominantly inherited blepharoptosis, high myopia and ectopia lentis. Arch Ophthalmol 1982; 100:282-284.
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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