Literature DB >> 33442089

Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES) Type 1 in an Indian Family.

Abhinav Kumar Gupta1, Deepak Chand Gupta1, Saqib Ahmad Khan1, Syed Mohd Razi2.   

Abstract

Blepharophimosis ptosis epicanthus inversus (BPES) is a relatively rare congenital disorder, which usually presents with classical eye manifestations. In some cases, it is associated with premature ovarian failure (POF). BPES is of two types, type I and type II. Type I is associated with POF along with eyelid malformations, while Type 2 has only eyelid malformations. Here, we report a family of BPES, in whom two sisters presented with secondary amenorrhea. On eye examination, they have blepharophimosis, ptosis, epicanthus inversus and telecanthus. Investigations revealed hypergonadotropic hypogonadism. Their father also has similar eye manifestations. Diagnosis of BPES type I was made and both were started on hormone replacement therapy. To make timely diagnosis of BPES, every patient with POF should specifically be checked for eye manifestations.
© 2017 Journal of the ASEAN Federation of Endocrine Societies.

Entities:  

Keywords:  blepharophimosis ptosis epicanthus inversus syndrome (BPES); primary ovarian failure; secondary amenorrhea

Year:  2017        PMID: 33442089      PMCID: PMC7784145          DOI: 10.15605/jafes.032.01.13

Source DB:  PubMed          Journal:  J ASEAN Fed Endocr Soc        ISSN: 0857-1074


  10 in total

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Journal:  Pediatr Endocrinol Rev       Date:  2005-06

2.  A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23.

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3.  An association among blepharophimosis, resistant ovary syndrome, and true premature menopause.

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Journal:  Fertil Steril       Date:  1988-11       Impact factor: 7.329

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Journal:  Hum Reprod       Date:  1994-11       Impact factor: 6.918

5.  Anthropometry of the eyelid and palpebral fissure in an Indian population.

Authors:  Surendra B Patil; Satish M Kale; Mahantesh Math; Nishant Khare; Jaiswal Sumeet
Journal:  Aesthet Surg J       Date:  2011-03       Impact factor: 4.283

6.  A new FOXL2 gene mutation in a woman with premature ovarian failure and sporadic blepharophimosis-ptosis-epicanthus inversus syndrome.

Authors:  Frederico José Silva Corrêa; Adriano Bueno Tavares; Rinaldo Wellerson Pereira; Mauricio Simões Abrão
Journal:  Fertil Steril       Date:  2009-12-06       Impact factor: 7.329

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Journal:  Am J Hum Genet       Date:  1983-09       Impact factor: 11.025

8.  Blepharophimosis, ptosis, epicanthus inversus, and primary amenorrhea. A dominant trait.

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Journal:  Arch Ophthalmol       Date:  1979-09

9.  Clinical, radiologic, and genetic features in blepharophimosis, ptosis, and epicanthus inversus syndrome in the Indian population.

Authors:  Bhavna Chawla; Yogesh Bhadange; Rima Dada; Manoj Kumar; Sanjay Sharma; Mandeep S Bajaj; Neelam Pushker; Mahesh Chandra; Supriyo Ghose
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-04-26       Impact factor: 4.799

10.  The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome.

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Journal:  Nat Genet       Date:  2001-02       Impact factor: 38.330

  10 in total
  1 in total

1.  Blepharophimosis, Ptosis, and Epicanthus Inversus Syndrome: A Simple Remedy for Challenging Cases.

Authors:  Saba Alkhairy; Hania Saeed; Samir Saeed
Journal:  Cureus       Date:  2022-07-29
  1 in total

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