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A case of Hirschsprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): potential map** of one disease locus

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Summary

A mentally retarded boy with discrete physical findings, Hirschsprung disease (HD) and a microdeletion of 13q,del(13)(q32.3q33.2) is described. Band 13q33.1 was consistently missing in all cells. There have been, to date, 4 published cases of deletions involving the long arm of chromosome 13 associated with HD: the interstitial deletion reported here is much smaller than, and it partially overlaps with, the previously reported deletions; it could be helpful for map** one of the genes involved in this disease.

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Bottani, A., ** of one disease locus. Hum Genet 87, 748–750 (1991). https://doi.org/10.1007/BF00201741

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  • DOI: https://doi.org/10.1007/BF00201741

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