A Case Report on Ankyloblepharon Filiforme Adnatum

Background: Ankyloblepharon filiforme adnatum is a rare congenital anomaly characterized by partial or complete adhesion of upper and lower eyelids. This condition is usually observed as an isolated finding; however, it is often associated with other anomalies or a well-defined syndrome. The etiolog...

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Main Authors: F Eslami, B Ebrahimi, P Khatibian, S Akbarzade
Format: Article
Language:fas
Published: Hamadan University of Medical Sciences 2017-12-01
Series:پزشکی بالینی ابن سینا
Subjects:
Online Access:http://sjh.umsha.ac.ir/article-1-1568-en.html
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spelling doaj-5bce09f0124c481abf2dbeca5d2b471e2020-11-25T04:10:45ZfasHamadan University of Medical Sciencesپزشکی بالینی ابن سینا2588-722X2588-72382017-12-01243259262A Case Report on Ankyloblepharon Filiforme AdnatumF Eslami0B Ebrahimi1P Khatibian2S Akbarzade3 Hamadan University of Medical Sciences Background: Ankyloblepharon filiforme adnatum is a rare congenital anomaly characterized by partial or complete adhesion of upper and lower eyelids. This condition is usually observed as an isolated finding; however, it is often associated with other anomalies or a well-defined syndrome. The etiology of this defect has not been identified yet. Case Presentation: Herein, we reported the case of a four-day-old male neonate who was unable to open his right eye at birth, which was due to adherent upper and lower eyelids as revealed in the physical examination. Family history of the patient was unremarkable. At sterile condition and under anesthesia, the adhesion of the eyelid was cut using a westcott scissor after holding the band of skin with forceps. Systemic and ocular examination did not reveal any abnormalities. Conclusion: Ankyloblepharon filiforme adnatum is a congenital anomaly that can lead to amblyopia. The accompaniment of this defect with other congenital abnormalities may account for mortality. The early treatment of this anomaly through a simple surgery prevents amblyopia.http://sjh.umsha.ac.ir/article-1-1568-en.htmlankyloblepharoncongenital anomalies
collection DOAJ
language fas
format Article
sources DOAJ
author F Eslami
B Ebrahimi
P Khatibian
S Akbarzade
spellingShingle F Eslami
B Ebrahimi
P Khatibian
S Akbarzade
A Case Report on Ankyloblepharon Filiforme Adnatum
پزشکی بالینی ابن سینا
ankyloblepharon
congenital anomalies
author_facet F Eslami
B Ebrahimi
P Khatibian
S Akbarzade
author_sort F Eslami
title A Case Report on Ankyloblepharon Filiforme Adnatum
title_short A Case Report on Ankyloblepharon Filiforme Adnatum
title_full A Case Report on Ankyloblepharon Filiforme Adnatum
title_fullStr A Case Report on Ankyloblepharon Filiforme Adnatum
title_full_unstemmed A Case Report on Ankyloblepharon Filiforme Adnatum
title_sort case report on ankyloblepharon filiforme adnatum
publisher Hamadan University of Medical Sciences
series پزشکی بالینی ابن سینا
issn 2588-722X
2588-7238
publishDate 2017-12-01
description Background: Ankyloblepharon filiforme adnatum is a rare congenital anomaly characterized by partial or complete adhesion of upper and lower eyelids. This condition is usually observed as an isolated finding; however, it is often associated with other anomalies or a well-defined syndrome. The etiology of this defect has not been identified yet. Case Presentation: Herein, we reported the case of a four-day-old male neonate who was unable to open his right eye at birth, which was due to adherent upper and lower eyelids as revealed in the physical examination. Family history of the patient was unremarkable. At sterile condition and under anesthesia, the adhesion of the eyelid was cut using a westcott scissor after holding the band of skin with forceps. Systemic and ocular examination did not reveal any abnormalities. Conclusion: Ankyloblepharon filiforme adnatum is a congenital anomaly that can lead to amblyopia. The accompaniment of this defect with other congenital abnormalities may account for mortality. The early treatment of this anomaly through a simple surgery prevents amblyopia.
topic ankyloblepharon
congenital anomalies
url http://sjh.umsha.ac.ir/article-1-1568-en.html
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