References
Hunter AGW, Partington MW, Evans JA. The Coffin-Lowry syndrome. Experience from four centres.Clin Genet 1982; 21: 321–335.
Jones KL.Smith's Recognizable Patterns of Human Malformation. Philadelphia: W.B. Saunders Company; 1988: 236–239.
Haspeslang M, Fryns JP, Beusen L et al. The Coffin-Lowry syndrome. A study of new index patients and their families.Eur J Pediatr 1984; 143: 82–86.
Vles JS, Haspeslagh M, Raes MM et al. Early clinical sings in Coffin Lowry syndrome.Clin Genet 1984; 26: 448–452.
Proud VK, Levine C, Carpenter NJ. New X-linked syndrome with seizures, acquired microencephaly, and agenesis of the corpus callosum.Am J Med Genet 1992; 43: 458–466.
Padley S, Hodgson SV, Sherwood T. The radiology of Coffin-Lowry syndrome.Br J Radiol 1990; 63: 72–75.
Kavukcu S, Diren B, Irken G et al. MR imaging of callosal and corticocallosal dysgenesis.Cocuk Sagligi ve Hastaliklari Dergisi 1992; 35: 123–129.
Barkovich AJ, Lyon G, Evrard P. Formation, maturation, and disorders of white matter.AJNR 1992; 13: 447–461.
Kolodny EH. Agenesis of the corpus callosum: A marker for inherited metabolic disease?Neurology 1989; 39: 847–848.
McKusick VN.Mendelian Inheritance in Man. Baltimore: The Johns Hopkins University Press; 1989: 1266–1267.
Beck M, Glössl J, Rüter R et al. Abnormal proteodermatan sulfate in three patients with Coffin-Lowry syndrome.Pediatr Res 1983; 17: 926–929.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Özden, A., Dirik, E., Emel, A. et al. Callosal dysgenesis in a patient with Coffin-Lowry syndrome. Indian J Pediatr 61, 101–103 (1994). https://doi.org/10.1007/BF02753570
Issue Date:
DOI: https://doi.org/10.1007/BF02753570