Congenital camptodactyly associated with the 48,XXYY syndrome
Bosch, A.M.; Hack, W.W.; Schrander-Stumpel, C.T.
Genetic Counseling 9(1): 19-21
1998
ISSN/ISBN: 1015-8146 PMID: 9555582 Document Number: 496815
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.
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