The aim of this article is to discuss about rare representation of ankyloblepharon (an established chromosomal anomaly with aberration of p53 inherited as an autosomal dominant trait) with cleft of palate without any other feature of ectodermal dysplasia. The need to surgically address ankyloblepharon in order to avoid complications is also discussed.
HasnerV. Ankyloblepharon filiforme adnatum. Z Heilkd. 1881;2(4):429.
2.
AmusiniPBruelHChabrolleJPel ForzliFLevesqueL. [Filiform ankyloblepharon adnatum]. Archives De Pediatrie: Organe Officiel De La Societe Francaise De Pediatrie. 2000;7(9):1009‐1010. https://doi.org/10.1016/s0929-693x(00)90023-x
3.
McGrathJADuijfPHDoetschV, et al.Hay–wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63. Hum Mol Genet. 2001;10(3):221‐229.
4.
Duke-ElderS. Part 2. Vol. 3. London: Henry Kimpton; 1964. System of Ophthalmology; p. 869.
5.
RosenmanYRonenSEidelmanAISchimmelMS. Ankyloblepharon filiforme adnatum: Congenital eyelid band syndromes. Am J Dis Child. 1980;134(8):751‐753.