Abstract
Clinical and dermatoglyphic data on a male patient with complete trisomy 8 are reported and compared with those of other known cases of trisomy 8. The more discriminating findings for this condition are skeletal anomalies, restricted articular function, and speech problems.
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- Fineman R. M., Ablow R. C., Howard R. O., Albright J., Breg W. R. Trisomy 8 mosaicism syndrome. Pediatrics. 1975 Nov;56(5):762–767. [PubMed] [Google Scholar]
- Jacobsen P., Mikkelsen M., Rosleff F. The trisomy 8 syndrome: report of two further cases. Ann Genet. 1974 Jun;17(2):87–94. [PubMed] [Google Scholar]
- Kakati S., Nihill M., Sinha A. K. An attempt to establish trisomy 8 syndrome. Humangenetik. 1973 Sep 20;19(3):293–300. doi: 10.1007/BF00278406. [DOI] [PubMed] [Google Scholar]
- Schaumann B. Dermatoglyphics in trisomy 8 mosaicism. Humangenetik. 1974;24(3):201–205. doi: 10.1007/BF00283585. [DOI] [PubMed] [Google Scholar]
- Sperber M. A. Schizophrenia and organic brain syndrome with trisomy 8 (group-C trisomy 8 [47, XX, 8+]). Biol Psychiatry. 1975 Feb;10(1):27–43. [PubMed] [Google Scholar]
- de Grouchy J., Josso F., Beguin S., Turleau C., Jalbert P., Laurent C. Déficit en facteur VII de la coagulation chez trois sujets trisomiques 8. Ann Genet. 1974 Jun;17(2):105–108. [PubMed] [Google Scholar]