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Its classical clinical manifestations are hyperandrogenism, ovulatory dysfunction bound to menstrual irregularities, and polycystic ovarian morphology
This can lead to the depletion of glutathione, further compromising the body's ability to detoxify toxins and heavy metals
Familial IPF accounts for less than 5% of the total of patients with IPF and is clinically and histologically indistinguishable from sporadic IPF
Nappo F, De Rosa N, Marfella R, De Lucia D, Ingrosso D, Perna AF, Farzati B, and Giugliano D (1999)
The diagnostic description of such features may provide valuable feedback and reassurance to the clinician