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Congenital camptodactyly associated with the 48,XXYY syndrome
A M Bosch1, W W Hack, C T Schrander-Stumpel
1Department of Pediatrics, Medical Centre Alkmaar, The Netherlands.
Genetic Counseling (Geneva, Switzerland)
|April 29, 1998
Abstract:
A male premature infant presented with slow development and congenital camptodactyly of both hands. Chromosome analysis showed a 48,XXYY karyotype. As far as we know, this is the first report describing congenital camptodactyly associated with the 48,XXYY syndrome.