Achondroplasia: Unexpected familial recurrence
- 1 October 1984
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 19 (2) , 245-250
- https://doi.org/10.1002/ajmg.1320190206
Abstract
We review six families in which recurrence of achondroplasia, inexplicable through autosomal dominant inheritance, has occurred. The clinical and radiographic characteristics of affected individuals in these families are identical to those usually seen in achondroplasia. Family histories and parental characteristics likewise seemed not to set this group apart from others with achondroplasia. While various mechanisms for these occurrences of achondroplasia in family members related through unaffected relatives can be postulated, the hypothesis that these recurrences were simply the result of two independent chance events cannot, at least for the moment, be excluded.Keywords
This publication has 9 references indexed in Scilit:
- Germinal mosaicism in achondroplasia: a family with 3 affected siblings of normal parentsClinical Genetics, 1983
- Achondroplasia and hypochondroplasia. Comments on frequency, mutation rate, and radiological features in skull and spine.Journal of Medical Genetics, 1979
- Delayed Mutation as a Cause of Genetic Disease in Man: Achondroplasia and the Wiedemann-Beckwith SyndromePublished by Springer Nature ,1977
- A new estimate of the achondroplasia mutation rateClinical Genetics, 1977
- Older paternal age and fresh gene mutation: Data on additional disordersThe Journal of Pediatrics, 1975
- Achondroplasia—a genetic and statistical surveyAnnals of Human Genetics, 1970
- Neurological abnormalities in achondroplastic childrenThe Journal of Pediatrics, 1967
- ACHONDROPLASIAAmerican Journal of Roentgenology, 1967