Cargando…
Congenital Tarsal Kink Syndrome: Literature Review and Case Report
Background: The congenital tarsal kink syndrome is a rare form of congenital upper eyelid entropion associated with cardiovascular, musculoskeletal or central nervous system disorders. This syndrome must be recognized and surgically treated as a perinatal emergency to avoid associated complications—...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774314/ https://www.ncbi.nlm.nih.gov/pubmed/35053656 http://dx.doi.org/10.3390/children9010031 |
_version_ | 1784636310844080128 |
---|---|
author | Schmitzer, Speranța Haidu, Sorin-Dorin Popteanu, Ioana Claudia Simionescu, Anca Angela |
author_facet | Schmitzer, Speranța Haidu, Sorin-Dorin Popteanu, Ioana Claudia Simionescu, Anca Angela |
author_sort | Schmitzer, Speranța |
collection | PubMed |
description | Background: The congenital tarsal kink syndrome is a rare form of congenital upper eyelid entropion associated with cardiovascular, musculoskeletal or central nervous system disorders. This syndrome must be recognized and surgically treated as a perinatal emergency to avoid associated complications—corneal ulcer, corneal leucoma, secondary amblyopia and decreased vision among children. Methods: A literature review was conducted to clarify the diagnosis particularities and the corrective surgery options of the congenital entropion on the upper eyelid. Results: Four relevant studies were found by researching the Web of Science and PubMed databases up to November 2021 for “congenital tarsal kink syndrome” and “congenital upper eyelid entropion”. Conclusions: In this paper, we present a case of congenital unilateral entropion of the upper left eyelid in the context of a tarsal kink syndrome in a one-month old infant, manifested by the absence of eyelashes on the upper eyelid of the left eye, hyperlacrimation and conjunctival hyperemia. Essential in managing the upper eyelid entropion is protecting the cornea. Furthermore, correcting a tarsal kink is eminently surgical, choosing between open or closed procedures. Herein, we address the difficulty in the timely diagnosis of this uncommon condition and make formal recommendations based on all reported cases. |
format | Online Article Text |
id | pubmed-8774314 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87743142022-01-21 Congenital Tarsal Kink Syndrome: Literature Review and Case Report Schmitzer, Speranța Haidu, Sorin-Dorin Popteanu, Ioana Claudia Simionescu, Anca Angela Children (Basel) Case Report Background: The congenital tarsal kink syndrome is a rare form of congenital upper eyelid entropion associated with cardiovascular, musculoskeletal or central nervous system disorders. This syndrome must be recognized and surgically treated as a perinatal emergency to avoid associated complications—corneal ulcer, corneal leucoma, secondary amblyopia and decreased vision among children. Methods: A literature review was conducted to clarify the diagnosis particularities and the corrective surgery options of the congenital entropion on the upper eyelid. Results: Four relevant studies were found by researching the Web of Science and PubMed databases up to November 2021 for “congenital tarsal kink syndrome” and “congenital upper eyelid entropion”. Conclusions: In this paper, we present a case of congenital unilateral entropion of the upper left eyelid in the context of a tarsal kink syndrome in a one-month old infant, manifested by the absence of eyelashes on the upper eyelid of the left eye, hyperlacrimation and conjunctival hyperemia. Essential in managing the upper eyelid entropion is protecting the cornea. Furthermore, correcting a tarsal kink is eminently surgical, choosing between open or closed procedures. Herein, we address the difficulty in the timely diagnosis of this uncommon condition and make formal recommendations based on all reported cases. MDPI 2022-01-01 /pmc/articles/PMC8774314/ /pubmed/35053656 http://dx.doi.org/10.3390/children9010031 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Schmitzer, Speranța Haidu, Sorin-Dorin Popteanu, Ioana Claudia Simionescu, Anca Angela Congenital Tarsal Kink Syndrome: Literature Review and Case Report |
title | Congenital Tarsal Kink Syndrome: Literature Review and Case Report |
title_full | Congenital Tarsal Kink Syndrome: Literature Review and Case Report |
title_fullStr | Congenital Tarsal Kink Syndrome: Literature Review and Case Report |
title_full_unstemmed | Congenital Tarsal Kink Syndrome: Literature Review and Case Report |
title_short | Congenital Tarsal Kink Syndrome: Literature Review and Case Report |
title_sort | congenital tarsal kink syndrome: literature review and case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774314/ https://www.ncbi.nlm.nih.gov/pubmed/35053656 http://dx.doi.org/10.3390/children9010031 |
work_keys_str_mv | AT schmitzersperanta congenitaltarsalkinksyndromeliteraturereviewandcasereport AT haidusorindorin congenitaltarsalkinksyndromeliteraturereviewandcasereport AT popteanuioanaclaudia congenitaltarsalkinksyndromeliteraturereviewandcasereport AT simionescuancaangela congenitaltarsalkinksyndromeliteraturereviewandcasereport |