Abstract
A 15-month-old male child with the Greig polysyndactyly-craniofacial dysmorphism syndrome is presented and the relevant literature is reviewed.
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Carpenter, G.: Two sisters showing malformations of the skull and other congenital abnormalities. Rep. Soc. Study Dis. Child Lond. 1, 110–114 (1901)
Greig, D. M.: Oxycephaly. Edinb. Med. J. 33, 189–218 (1926)
Hootnick, D., Holmes, L. B.: Familial polysyndactyly and craniofacial anomalies. Clin. Genet. 3, 128–134 (1972)
Marshall, R. E., Smith, D. W.: Frontodigital syndrome: a dominantly inherited disorder with normal intelligence. J. Pediat. 77, 129–133 (1970)
Noack, M.: Ein Beitrag zum Krankheitsbild der Akrozephalosyndactylie (Aper). Arch. Kinderheilk. 160, 169–171 (1959)
Robinow, M., Sorauf, T. J.: Acrocephalopoly-syndactyly, type Noack in a large kindred. Birth Defects, Original Article Series, XI, 5, 99–106 (1975)
Temtamy, S. A.: Carpenter's syndrome: Acrocephalopolysyndactyly, an autosomal recessive syndrome. J. Pediat. 69, 111–120 (1966)
Temtamy, S., McKusick, V. A.: Synopsis on hand malformations with particular emphasis on genetic factors. Birth Defects, Original Article Series V, 3, 125–184 (1969)
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Fryns, J.P., Coeck, W. & van den Berghe, H. The Greig polysyndactyly-craniofacial dysmorphism syndrome. Eur J Pediatr 126, 283–287 (1977). https://doi.org/10.1007/BF00477055
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DOI: https://doi.org/10.1007/BF00477055