Crome Syndrome &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; &n 414f59e bsp; 325
General: Fatal; death usually at 4 to 8 months; autosomal recessive.
Ocular: Congenital cataracts.
Clinical: Epileptic seizures; mental retardation; small stature; renal tubular necrosis; encephalopathy.
Crome L, et al. Congenital cataracts, renal tubular necrosis and encephalopathy in two sisters. Arch Dis Child 1963; 38:505-515.
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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