Francois Syndrome (2) (Dystrophia Dermachondrocornealis Familiaris) 4
General: Autosomal recessive.
Ocular: Central superficial corneal dystrophy with subepithelial opacities.
Clinical: Distal osteochondral dystrophy of the extremities; cutaneous xanthomas.
Caputo R, et al. Dermatochondrocorneal dystrophy (Francois' syndrome): report of a case. Arch Dermatol 1988; 124: 424-428.
Francois J. Dystrophic Dermo-Chondro-Corneenne Familiale. Ann Ocul (Paris) 1949; 182:409-442.
Jablonski S. Eponymic syndromes and diseases. Philadelphia: WB Saunders, 1969.
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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