Abstract
GOODMAN syndrome, or Tel-Hashomer camptodactyly, comprises digital contractures, a distinctive facies, muscular hypoplasia and multiple skeletal abnormalities. Inheritance is autosomal recessive.
This is a preview of subscription content, log in via an institution to check access.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Goodman RM, Katznelson MB, Manor E (1972) Camptodactyly: occurrence in two new genetic syndromes and its relationship to other syndromes. J Med Genet 9: 203-212
Goodman RM, Katznelson M, Katznelson A (1976) Camptodactyly with muscular hypoplasia, skeletal dysplasia and abnormal palmar creases: Tel-Hashomer camptodactyly syndrome. J Med Genet 13:136-141
Goodman RM, Sternberg M, Shem-Tow Y, Katznelson MB, Hertz M, Rotem Y (1979) Acrocephalopolysyndactyly type IV: a new genetic syndrome in 3 sibs. Clin Genet 15: 209-214
McKusick VA (1992) Mendelian Inheritance in Man. 10th Edn. Johns Hopkins University Press, Baltimore & London, p. 1181
Cohen DM, Green JG, Miller J, Gorlin RJ, Reed JA (1987) Acrocephalopolysyndactyly type II - Carpenter syndrome: clinical spectrum and an attempt at unification with Goodman and Summitt syndromes. Am J Med Genet 28: 311-324
Obituary (Comings DE) (1991) Am J Med Genet 38: 517
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 1997 Springer-Verlag London Limited
About this chapter
Cite this chapter
Beighton, P., Beighton, G. (1997). GOODMAN,Richard M. In: The Person Behind the Syndrome. Springer, London. https://doi.org/10.1007/978-1-4471-0925-9_32
Download citation
DOI: https://doi.org/10.1007/978-1-4471-0925-9_32
Publisher Name: Springer, London
Print ISBN: 978-1-4471-1236-5
Online ISBN: 978-1-4471-0925-9
eBook Packages: Springer Book Archive