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The genetics of cri du chat syndrome do not follow the classic patterns of mendelian inheritance. This is a congenital (rather than "hereditary") abnormality involiving a partial deletion of the short arm of chromosome 5. Approximately 85% of cases result from sporadic de novo deletions, while 15% arise secondary to unequal segregation of a parental translocation.

2007-03-17 05:44:53 · answer #1 · answered by Anonymous · 1 0

I don't think it's either. it's caused by a missing part of a gene and is not hereditary. it's a chromosomal abnormality.

2007-03-17 12:32:53 · answer #2 · answered by wendy_da_goodlil_witch 7 · 0 1

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