PMID: 9182784Jun 27, 1997Paper

XX-agonadism in a fetus with multiple dysraphic lesions: a new syndrome

American Journal of Medical Genetics
I KennerknechtW Vogel

Abstract

We report on a 19-week-old fetus with a 46,XX karyotype, normal female external genitalia, complete gonadal agenesis, large encephalocele, spina bifida, and omphalocele. We postulate a new syndrome. Hitherto no consistent malformation patterns have been observed in agonadism patients. True agonadism, including even the unusual finding of an XX gonosomal status, is obviously not as rare as suggested.

References

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Citations

Oct 22, 2008·Taiwanese Journal of Obstetrics & Gynecology·Chih-Ping Chen
Mar 25, 2004·American Journal of Medical Genetics. Part a·Hennie H N WooC H Tang

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