Gonadal agenesis 46,XX associated with the atypical form of Rokitansky syndrome
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology,Reproductive Medicine
Reference4 articles.
1. Mayer-Rokitansky-Küster-Hauser syndrome;Strubbe;Am J Roentgenol,1993
2. Vaginal agenesis (Mayer-Rokitansky-Küster-Hauser syndrome) associated with the N314D mutation of galactose-1-phosphate uridyl transferase (GALT);Cramer;Mol Hum Reprod,1996
3. An XX female with sexual infantilism, absent gonads and lack of Müllerian ducts;Levinson;J Med Genet,1976
4. Gonadal dysgenesis and Rokitansky syndrome. A case report;Guitron Cantu;J Reprod Med,1999
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1. MRI presentations of Müllerian duct anomalies in association with unilateral renal agenesis;Clinical Radiology;2023-03
2. Misdiagnosis of Mullerian Agenesis in a Patient with 46, XX Gonadal Dysgenesis;The Misdiagnosis Casebook in Clinical Medicine;2023
3. A rare case of 46,XX gonadal dysgenesis, Mayer–Rokitansky–Kuster–Hauser syndrome, pituitary and thyroid hypoplasia;Endocrinology, Diabetes & Metabolism Case Reports;2022-02-01
4. Protein–protein interaction network analysis applied to DNA copy number profiling suggests new perspectives on the aetiology of Mayer–Rokitansky–Küster–Hauser syndrome;Scientific Reports;2021-01-11
5. Mayer-Rokitansky-Künster-Hauser syndrome due to 2q12.1q14.1 deletion: PAX8 the causing gene?;European Journal of Medical Genetics;2020-04
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