Agnathia, holoprosencephaly, and situs inversus: A third report
- 1 October 1990
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 37 (2) , 286-287
- https://doi.org/10.1002/ajmg.1320370226
Abstract
We report on a male infant with cyclopia, agnathia, and situs inversus. In addition, anal atresia and horseshoe‐kidneys were present. To our knowledge, this is the third published case of the “agnathia‐holoprosencephaly‐further midline defects association”.Keywords
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