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FSHR gene mutation
Clinical significance:
- defects in FSHR are a cause of
a) ovarian dysgenesis 1
b) ovarian hyperstimulation syndrome
- activating mutations of the FSH receptor:
-> fertile eunuch syndrome
Related
follicle-stimulating hormone receptor; FSH-R; follitropin receptor (FSHR, LGR1)
General
gene mutation testing; gene mutation analysis
References
Loinc