A Pellino‐2 variant is associated with constitutive NLRP3 inflammasome activation in a family with ocular pterygium–digital keloid dysplasia
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DOI: 10.1002/1873-3468.14597
Abstract: Ocular pterygium–digital keloid dysplasia (OPDKD) is a rare hereditary disease characterized by corneal ingrowth of vascularized conjunctival tissue early in life. Later, patients develop keloids on fingers and toes but are otherwise healthy. In a… read more here.
Keywords: keloid dysplasia; pellino; pterygium digital; ocular pterygium ... See more keywords