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Mullerian Aplasia and Hyperandrogenism

Known as: Mullerian Duct Failure and Hyperandrogenism, WNT4 Deficiency 
Deficiency of the glycoprotein WNT4, associated with loss of function mutation(s) in the WNT4 gene. The condition in 46,XX individuals is… 
National Institutes of Health

Related topics

Related topics

6 relations
AcneAutosomal dominant inheritanceEndocrine systemPrimary physiologic amenorrhea

Broader (2)

HyperandrogenismStructure of paramesonephric duct

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
Association between biochemical hyperandrogenism parameters and Ferriman‐Gallwey score in patients with polycystic ovary syndrome: A systematic review and meta‐regression analysis
A limited number of studies have evaluated the relationship between clinical and biochemical hyperandrogenism (HA). This study… 
2017
2017
A Case-controlled Comparative Hospital-based Study on the Clinical, Biochemical, Hormonal, and Gynecological Parameters in Polycystic Ovary Syndrome
The objective of this study was to evaluate and compare the clinical, biochemical, hormonal and gynecological aspects of… 
2014
2014
Wnt4, a pleiotropic signal for controlling cell polarity, basement membrane integrity, and antimullerian hormone expression during oocyte maturation in the female follicle
Wnt4 is a key signal that channels the developmental fate of the indifferent mammalian gonad toward the ovary, but whether Wnt4… 
2008
2008
Monogenic and Polygenic Models Detected in Steroid 21-Hydroxylase Deficiency-Related Paediatric Hyperandrogenism
Aims: Hyperandrogenism, although mostly due to polygenic interactions, is monogenic for some enzymatic adrenal deficiencies. This… 
Review
1998
Review
1998
[Managing hyperandrogenism].
1956
1956
[Various unpublished forms of feminine hyperandrogenism].
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