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

  • Matthias Möhrenschlager
  • , Dirk B. Wessner
  • , Dietrich Abeck
  • , Johannes Ring
  • Technical University of Munich

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

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 languageEnglish
Pages (from-to)58-59
Number of pages2
JournalJournal of AAPOS
Volume5
Issue number1
DOIs
StatePublished - Feb 2001

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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