Falciform Detachment
General: Autosomal dominant or recessive; preperinatally acquired; characterized by ocular signs only; falciform detachment and congenital total detachment may alternate in affected siblings; falciform detachment and folds; retina projects as a wedge-shaped fold from the posterior pole of eye into the vitreous, occasionally as far anterior as the lens; less typical fold flattens and tapers out in the midperiphery of the retina.
Ocular: Falciform folds; retinal detachment; retrolental fibroplasia.
Clinical: None.
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/.
Warburg M. Heterogeneity of congenital retinal non-attachment falciform folds and retinal dysplasia: a guide to genetic counseling. Hum Hered 1976; 26:137-l48.
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