Blepharoptosis, Myopia, Ectopia Lentis &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; &n 212g63c bsp; 156
General: Autosomal dominant.
Ocular: Ptosis; high-grade myopia; ectopia lentis; displacement of crystalline lens of eye; connective tissue defect of sclera, zonules, and levator aponeurosis.
Clinical: None.
Gillum WN, et al. 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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