2013
DOI: 10.1016/j.det.2012.08.005
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Hair: What is New in Diagnosis and Management?

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Cited by 52 publications
(19 citation statements)
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“…[2] Estrogen and androgens are the main hormones that regulate the development of FPHL. [1] In addition to sex hormones, FPHL can be associated with insulin resistance, microvascular, and inflammatory disorders. Insulin resistance reduces sex hormone-binding globulin in circulation that leads to early-onset androgenetic alopecia in men.…”
Section: Discussionmentioning
confidence: 99%
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“…[2] Estrogen and androgens are the main hormones that regulate the development of FPHL. [1] In addition to sex hormones, FPHL can be associated with insulin resistance, microvascular, and inflammatory disorders. Insulin resistance reduces sex hormone-binding globulin in circulation that leads to early-onset androgenetic alopecia in men.…”
Section: Discussionmentioning
confidence: 99%
“…Insulin resistance reduces sex hormone-binding globulin in circulation that leads to early-onset androgenetic alopecia in men. [1] Miniaturization of hair follicles together with diffuse hair loss in frontal lobe can be seen in women without increased levels of androgens, which justifies the lack of response to androgen inhibitors in some women with FPHL. [34] On the other hand, FPHL cases in patients with complete androgen insensitivity syndromes support the involvement of other factors in FPHL pathogenesis.…”
Section: Discussionmentioning
confidence: 99%
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“…It is well known that androgens affect the growth of the scalp and body hair and even Hippocrates observed 2,400 years ago that eunuchs did not experience baldness (Yip et al, 2011). However, hyperandrogenism cannot be the only pathophysiologic mechanism for FPHL because the majority of women with FPHL neither have abnormal androgen levels nor do they demonstrate signs or symptoms of androgen excess (Atanaskova Mesinkovska and Bergfeld, 2013, Schmidt and Shinkai, 2015, Yip et al, 2011). Furthermore, cases have been reported in which FPHL developed in patients with complete androgen insensitivity syndrome or hypopituitarism with no detectable androgen levels (Cousen and Messenger, 2010, Orme et al, 1999).…”
Section: Pathophysiologymentioning
confidence: 99%