Case Reports
doi: 10.1002/ajmg.1320120209.
The acrocallosal syndrome
- PMID: 7102724
- DOI: 10.1002/ajmg.1320120209
Item in Clipboard
Case Reports
The acrocallosal syndrome
Am J Med Genet.
1982 Jun.
Abstract
We report two unrelated patients, a three-year-old girl and an 88/12 year-old boy with the newly described "acrocallosal" syndrome. The main manifestations of the syndrome are unusual facial appearance, pre- and postaxial polydactyly, mental retardation, and absence of the corpus callosum. Cause remains unknown.
Similar articles
-
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):241-9. doi: 10.1002/ajmg.1320060308. Am J Med Genet. 1980. PMID: 7424976
-
Hypogenitalism in the acrocallosal syndrome.Am J Med Genet. 1989 Mar;32(3):301-5. doi: 10.1002/ajmg.1320320304. Am J Med Genet. 1989. PMID: 2658583 Review.
-
Greig cephalopolysyndactyly syndrome with dysgenesis of the corpus callosum in a Bedouin family.Am J Med Genet. 1996 Dec 18;66(3):261-4. doi: 10.1002/(SICI)1096-8628(19961218)66:3<261::AID-AJMG4>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8985483
-
[Velo-cardio-facial syndrome (Shprintzen syndrome)].Pediatr Med Chir. 1984 Sep-Oct;6(5):695-7. Pediatr Med Chir. 1984. PMID: 6535135 Italian.
-
Acrocallosal syndrome: additional manifestations.Am J Med Genet. 1989 Mar;32(3):311-7. doi: 10.1002/ajmg.1320320306. Am J Med Genet. 1989. PMID: 2658584 Review.
Cited by
-
How wide is the clinical spectrum of the acrocallosal syndrome? Report of a mild case.J Med Genet. 1990 Aug;27(8):516-8. doi: 10.1136/jmg.27.8.516. J Med Genet. 1990. PMID: 2103730 Free PMC article.
-
Four patients including two sisters with the acrocallosal syndrome (agenesis of the corpus callosum in combination with preaxial hexadactyly).Hum Genet. 1982;62(4):382. doi: 10.1007/BF00304564. Hum Genet. 1982. PMID: 7166318 No abstract available.
-
Further delineation of the acrocallosal syndrome.Eur J Pediatr. 1991 Sep;150(11):797-9. doi: 10.1007/BF02026715. Eur J Pediatr. 1991. PMID: 1659985
-
The acrocallosal syndrome and Greig syndrome are not allelic disorders.J Med Genet. 1992 Sep;29(9):635-7. doi: 10.1136/jmg.29.9.635. J Med Genet. 1992. PMID: 1404293 Free PMC article.
-
A family with one child with acrocallosal syndrome, one child with anencephaly-polydactyly, and parental consanguinity.Eur J Pediatr. 1992 Apr;151(4):288-90. doi: 10.1007/BF02072231. Eur J Pediatr. 1992. PMID: 1499582
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources