Abstract
A boy presenting with an incomplete form of the acrocallosal syndrome is described. The syndrome shows clinical variability and it is stressed that none of the components is constant and facial dysmorphism is not always characteristic.
Full text
PDF
Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Casamassima A. C., Beneck D., Gewitz M. H., Horowitz M. A., Woolf P. K., Pettersen I. M., Shapiro L. R. Acrocallosal syndrome: additional manifestations. Am J Med Genet. 1989 Mar;32(3):311–317. doi: 10.1002/ajmg.1320320306. [DOI] [PubMed] [Google Scholar]
- Moeschler J. B., Pober B. R., Holmes L. B., Graham J. M., Jr Acrocallosal syndrome: new findings. Am J Med Genet. 1989 Mar;32(3):306–310. doi: 10.1002/ajmg.1320320305. [DOI] [PubMed] [Google Scholar]
- Nelson M. M., Thomson A. J. The acrocallosal syndrome. Am J Med Genet. 1982 Jun;12(2):195–199. doi: 10.1002/ajmg.1320120209. [DOI] [PubMed] [Google Scholar]
- Philip N., Apicella N., Lassman I., Ayme S., Mattei J. F., Giraud F. The acrocallosal syndrome. Eur J Pediatr. 1988 Feb;147(2):206–208. doi: 10.1007/BF00442226. [DOI] [PubMed] [Google Scholar]
- Salgado L. J., Ali C. A., Castilla E. E. Acrocallosal syndrome in a girl born to consanguineous parents. Am J Med Genet. 1989 Mar;32(3):298–300. doi: 10.1002/ajmg.1320320303. [DOI] [PubMed] [Google Scholar]
- Sanchis A., Cerveró L., Martínez A., Valverde C. Duplication of hands and feet, multiple joint dislocations, absence of corpus callosum and hypsarrhythmia: acrocallosal syndrome? Am J Med Genet. 1985 Jan;20(1):123–130. doi: 10.1002/ajmg.1320200115. [DOI] [PubMed] [Google Scholar]
- Schinzel A., Kaufmann U. The acrocallosal syndrome in sisters. Clin Genet. 1986 Nov;30(5):399–405. doi: 10.1111/j.1399-0004.1986.tb01897.x. [DOI] [PubMed] [Google Scholar]
- Schinzel A. Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macrencephaly and severe mental retardation: a new syndrome? Helv Paediatr Acta. 1979 May;34(2):141–146. [PubMed] [Google Scholar]
- Schinzel A., Schmid W. Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome. Am J Med Genet. 1980;6(3):241–249. doi: 10.1002/ajmg.1320060308. [DOI] [PubMed] [Google Scholar]
- Schinzel A. The acrocallosal syndrome in first cousins: widening of the spectrum of clinical features and further support for autosomal recessive inheritance. J Med Genet. 1988 May;25(5):332–336. doi: 10.1136/jmg.25.5.332. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Temtamy S. A., Meguid N. A. Hypogenitalism in the acrocallosal syndrome. Am J Med Genet. 1989 Mar;32(3):301–305. doi: 10.1002/ajmg.1320320304. [DOI] [PubMed] [Google Scholar]