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

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 w...

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Autores principales: Gupta, Abhinav Kumar, Gupta, Deepak Chand, Khan, Saqib Ahmad, Razi, Syed Mohd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of the ASEAN Federation of Endocrine Societies 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784145/
https://www.ncbi.nlm.nih.gov/pubmed/33442089
http://dx.doi.org/10.15605/jafes.032.01.13
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author Gupta, Abhinav Kumar
Gupta, Deepak Chand
Khan, Saqib Ahmad
Razi, Syed Mohd
author_facet Gupta, Abhinav Kumar
Gupta, Deepak Chand
Khan, Saqib Ahmad
Razi, Syed Mohd
author_sort Gupta, Abhinav Kumar
collection PubMed
description 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.
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spelling pubmed-77841452021-01-12 Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES) Type 1 in an Indian Family Gupta, Abhinav Kumar Gupta, Deepak Chand Khan, Saqib Ahmad Razi, Syed Mohd J ASEAN Fed Endocr Soc Case Report 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. Journal of the ASEAN Federation of Endocrine Societies 2017-05-09 2017 /pmc/articles/PMC7784145/ /pubmed/33442089 http://dx.doi.org/10.15605/jafes.032.01.13 Text en © 2017 Journal of the ASEAN Federation of Endocrine Societies https://creativecommons.org/licenses/by-nc/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International.
spellingShingle Case Report
Gupta, Abhinav Kumar
Gupta, Deepak Chand
Khan, Saqib Ahmad
Razi, Syed Mohd
Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES) Type 1 in an Indian Family
title Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES) Type 1 in an Indian Family
title_full Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES) Type 1 in an Indian Family
title_fullStr Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES) Type 1 in an Indian Family
title_full_unstemmed Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES) Type 1 in an Indian Family
title_short Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES) Type 1 in an Indian Family
title_sort blepharophimosis ptosis epicanthus inversus syndrome (bpes) type 1 in an indian family
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784145/
https://www.ncbi.nlm.nih.gov/pubmed/33442089
http://dx.doi.org/10.15605/jafes.032.01.13
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