Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13)
- PMID: 2729360
- DOI: 10.1002/ajmg.1320320329
Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13)
Abstract
We report on cases of Greig syndrome segregating in a large kindred over four generations due to reciprocal translocation t(6;7)(q27;p13) and on a patient from this pedigree with a severe malformation syndrome due to duplication 7(p13----pter). The clinical findings are discussed as possible consequence of a gene mutation due to the break at 7p13.
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