Cutaneous peculiarities in blepharophimosis-ptosis-epicanthus inversus syndrome: Report of a case

Matthias Möhrenschlager; Dirk B. Wessner; Dietrich Abeck; Johannes Ring

doi:10.1067/mpa.2001.111781

Cutaneous peculiarities in blepharophimosis-ptosis-epicanthus inversus syndrome: Report of a case

Matthias Möhrenschlager, Dirk B. Wessner, Dietrich Abeck, Johannes Ring

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Technical University of Munich

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Abstract

Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) is a rare inherited disorder with characteristic oculofacial affection of the eyelid region. Recent results of genetic analysis of the causative gene, as well as a hitherto unknown association with hormone-dependent endometrial carcinoma, motivated us to review this syndrome.

Original language	English
Pages (from-to)	58-59
Number of pages	2
Journal	Journal of AAPOS
Volume	5
Issue number	1
DOIs	https://doi.org/10.1067/mpa.2001.111781
State	Published - Feb 2001

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abstract = "Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) is a rare inherited disorder with characteristic oculofacial affection of the eyelid region. Recent results of genetic analysis of the causative gene, as well as a hitherto unknown association with hormone-dependent endometrial carcinoma, motivated us to review this syndrome.",

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AU - Ring, Johannes

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AB - Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) is a rare inherited disorder with characteristic oculofacial affection of the eyelid region. Recent results of genetic analysis of the causative gene, as well as a hitherto unknown association with hormone-dependent endometrial carcinoma, motivated us to review this syndrome.

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Cutaneous peculiarities in blepharophimosis-ptosis-epicanthus inversus syndrome: Report of a case

Abstract

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