Abstract
A boy with Duchenne muscular dystrophy and facial dysmorphism in conjunction with Klinefelter's genotype 47XXY is presented; this is an unusual situation with two genetic errors evolving over two generations. Karyotyping should be considered in boys with Duchenne muscular dystrophy who have unusual features.
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CITATION STYLE
APA
Ramesh, V., Mountford, R., Kingston, H. M., Kelsey, A., Noronha, M. J., & Clarke, M. A. (1993). Occurrence of Duchenne dystrophy in Klinefelter’s syndrome. Archives of Disease in Childhood, 69(4), 453–454. https://doi.org/10.1136/adc.69.4.453
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