Congenital ankyloblepharon

Known as: Ankyloblepharon, Fused Eyelid, Fused eyelids 
A congenital abnormality in which the margins of the upper and lower eyelids are fused together by bands of tissue.
National Institutes of Health

Papers overview

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2011
2011
Heterozygous mutations of p63, a key transcription factor in epithelial development, are causative in a variety of human… (More)
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2009
2009
The transcription factor p63 plays a pivotal role in the development and differentiation of the epidermis and epithelial… (More)
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2006
2006
p63 is a developmentally regulated transcription factor related to p53, which activates and represses specific genes. The human… (More)
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2005
2005
This paper describes the use of amniotic membrane in the reconstructive surgical repair of generalized keratomalacia… (More)
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2004
2004
Van der Woude syndrome (VWS, OMIM #119300) is a dominantly inherited developmental disorder characterised by pits and/or sinuses… (More)
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Review
2002
Review
2002
The P63 gene is a recently discovered member of the p53 family. While P53 is ubiquitously expressed, p63 is expressed… (More)
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Highly Cited
2001
Highly Cited
2001
Hay-Wells syndrome, also known as ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome (OMIM 106260), is a rare autosomal… (More)
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1995
1995
A recently characterized integrin alpha-chain, alpha 9, forms heterodimers with the integrin beta 1-chain and is present in the… (More)
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Highly Cited
1993
Highly Cited
1993
The process of eyelid development was studied in the mouse. The critical events occur between about 15.5 d postcoitum (p.c.) and… (More)
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1976
1976
Seven patients from four families are reported who had an inherited condition of which the main features were ankyloblepharon… (More)
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