The Genetics of Hand Malformations: Updated*
- 1 March 1985
- journal article
- Published by Wiley in Congenital Anomalies
- Vol. 25 (1) , 73-92
- https://doi.org/10.1111/j.1741-4520.1985.tb00636.x
Abstract
The main values of our knowledge of the genetics of birth defects are proper diagnosis and counseling.A classification of hand malformations on anatomic and genetic grounds was proposed by Temtamy (1966), Temtamy and McKusick (1969, 1978): The ten main categories are (1) Absence, (2) Brachydactyly, (3) Syndactyly, (4) Polydactyly, (5) Symphalangism, (6) Arachnodactyly, (7) Macrodactyly, (8) Carpal/Tarsal synostosis, (9) Congenital ring constrictions, and (10) Contractures.The hand malformation is either isolated or associated with other organ malformation as a part of syndromes. In the monograph by Temtamy and McKusick (1978), numerous new syndromes were identified, some of which were based on single or few observations.The paper summerizes the pertinent findings in a computerized literature survey of absence or deficiency malformation as part of synderomes reported between 1977 and 1983.Analysis of the literature confirmed the identity of previously reported syndromes and added “new” entities.The originally proposed classification of hand malformations proved to be useful and allowed for easy sorting out of the recent literature and for indentification of new syndromes.Keywords
This publication has 63 references indexed in Scilit:
- Recurrence of the postaxial acrofacial dysostosis syndrome in a sibship: Implications for genetic counselingThe Journal of Pediatrics, 1981
- Postaxial acrofacial dysostosis syndromeThe Journal of Pediatrics, 1979
- Holt-Oram syndromeThe Journal of Pediatrics, 1979
- Autosomal dominant transmission of a syndrome of anal, ear, renal, and radial congenital malformationsThe Journal of Pediatrics, 1978
- A female patient with “Aase syndrome”The Journal of Pediatrics, 1977
- Familial anal abnormalityThe Journal of Pediatrics, 1976
- The syndrome of aplasia cutis congenita with terminal, transverse defects of limbsThe Journal of Pediatrics, 1975
- Triphalangeal thumbs and congenital erythroid hypoplasia: Report of a case with unusual featuresThe Journal of Pediatrics, 1972
- A new familial syndrome of oral, cranial, and digital anomaliesThe Journal of Pediatrics, 1969
- Simultaneous occurrence of the Holt-Oram and the Duane syndromesThe Journal of Pediatrics, 1966