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Hypotriploidy 68,XX: a new case report and review of earlier cases
Y M Hoedemaekers1, M J K De Kleine, M J P L Stevens-Kroef
1Department of Neonatology, Maxima Medisch Centrum Veldhoven, 5500 MB Veldhoven, The Netherlands.
Abstract:
We report a prematurely born patient with a 68,XX karyotype. She presented with syndactyly of 2nd and 3rd toes, minor facial features, microcephaly, slender hands, bicuspid aortic valve, patent ductus arteriosus and hypotonia. Comparison with other reported cases is given.
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