2000
DOI: 10.1159/000018368
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Male-Pattern Baldness in Men with X-Linked Recessive Ichthyosis

Abstract: Background: X-linked recessive ichthyosis (XRI) is a genetic disorder of keratinization with extracutaneous manifestations due to deficiency of steroid sulfatase (STS). Because STS plays an important role in androgen metabolism, and elevated levels of dehydroepiandrosterone sulfate have been reported in young men with andogenetic alopecia (AGA), the hypothesis was advanced that men with XRI do not show AGA or develop only mild forms of common baldness. Methods: Patients with a diagnosis of XRI confirmed by ana… Show more

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Cited by 16 publications
(5 citation statements)
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“…We concluded that an increased conversion of testosterone to 17β‐oestradiol, and andros‐ tendione to oestrone, takes place in hair follicles derived from the occiput under the influence of estradiol. In theory, this pathway may diminish the amount of intrafollicular testosterone available for conversion to DHT 39 …”
Section: Aromatasementioning
confidence: 99%
“…We concluded that an increased conversion of testosterone to 17β‐oestradiol, and andros‐ tendione to oestrone, takes place in hair follicles derived from the occiput under the influence of estradiol. In theory, this pathway may diminish the amount of intrafollicular testosterone available for conversion to DHT 39 …”
Section: Aromatasementioning
confidence: 99%
“…22 We conducted a survey of patients with XRI showing that this is not the case, since these men also showed advanced PHL. 23 …”
Section: Role Of Sexual Hormonesmentioning
confidence: 99%
“…Andere systematische Untersuchungen legen nahe,dass der Insulin-like Growth Factor (IGF-1) und das Insulin-like Growth Factor Binding Protein-(ILGBP-)3 als mögliche Faktoren bei der AGA-Entstehung eine Rolle spielen [64,78]. Eine Untersuchung auf molekularer Ebene steht für IGF-1 noch aus, obwohl wir wissen, dass das Insulingen [22] und auch das Gen der Steroidsulfatase [30,87] und das "hairless-Gen" [81] nicht für die Erblichkeit der AGA verantwortlich sind. Ein Fallbericht [49] diskutiert die Bedeutung des für die Adrenoleukodystrophie verantwortlichen Genes (PTS1 receptor gene,PXR1; 600414) oder des Peroxin-1-Gens (PEX1; 602136), da Adrenoleukodystrophiepatienten eine erheblich stärkere AGA aufweisen als die Normalbevölkerung.…”
Section: Vererbungunclassified