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Francois syndrome (2) (dystrophia dermachondrocornealis familiaris) 4


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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