How wide is the clinical spectrum of the acrocallosal syndrome? Report of a mild case.
Open Access
- 1 August 1990
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 27 (8) , 516-518
- https://doi.org/10.1136/jmg.27.8.516
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.Keywords
This publication has 12 references indexed in Scilit:
- Acrocallosal syndrome: Additional manifestationsAmerican Journal of Medical Genetics, 1989
- Acrocallosal syndrome: New findingsAmerican Journal of Medical Genetics, 1989
- Hypogenitalism in the acrocallosal syndromeAmerican Journal of Medical Genetics, 1989
- Acrocallosal syndrome in a girl born to consanguineous parentsAmerican Journal of Medical Genetics, 1989
- The acrocallosal syndrome in first cousins: widening of the spectrum of clinical features and further support for autosomal recessive inheritance.Journal of Medical Genetics, 1988
- The acrocallosal syndromeEuropean Journal of Pediatrics, 1988
- Duplication of hands and feet, multiple joint dislocations, absence of corpus callosum and hypsarrhythmia: Acrocallosal syndrome?American Journal of Medical Genetics, 1985
- The acrocallosal syndromeAmerican Journal of Medical Genetics, 1982
- Acrocallosal syndromeAmerican Journal of Medical Genetics, 1982
- Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: A new syndromeAmerican Journal of Medical Genetics, 1980