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J-GLOBAL ID:200902252500146487   Reference number:03A0305501

A Case of Coffin-Lowry Syndrome

歯槽骨吸収を伴うCoffin-Lowry症候群の1症例
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Material:
Volume: 41  Issue:Page: 303-309  Publication year: Mar. 25, 2003 
JST Material Number: Y0025A  ISSN: 0583-1199  Document type: Article
Article type: 短報  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Congenital diseases,deformities in general.  ,  Diseases of tooth and mouth(=oral cavity) 
Reference (18):
  • 1) Coffin, G. S., Siris, E. and Wegienka, L. C.: Mental retardation with osteocartilaginous anomalies, Am. J. Dis. Child., 112: 205-213, 1966.
  • 2) Lowry, R. B., Miller, J. R. and Fraser, F. C.: A new dominant gene mental retardation syndrome: Associated with small stature, tapering fingers, characteristic faces and possible hydrocephalusA, m. J. Dis. Child., 121: 491-500, 1971.
  • 3) Temtamy, S. A., Miller, J. D. and Hussels-MaumeneeL,.: The Coffin-Lowry syndrome: An inherited faciodigital mental retardation syndrome, J. Pediatr., 86: 724-731, 1975.
  • 4) Biancalana, V., Braird, M. L. and David, A.: Confirmation and refinement of the genetic localization of Coffin-Lowry syndrome locus in Xp 22.1-p 22.2, Am. J. Hum. Genet., 50: 981-987, 1992.
  • 5) Trivier, E., DeCesare, D. and Jacquot, S.: Mutations in the kinase RSK-2 associated with Coffin-Lowry syndrome, Nature. 384: 567-570. 1996.
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