parakeratosis.The molecular defect has yet to be identified.AcrokeratoelastoidosisSynonyms include punctate PPK type III, focal acral hyperkeratosis, or acrokeratoelastoidosis of Costa. Acrokeratoelastoidosis is usually sporadic, although familial cases suggest an autosomal dominant pattern of inheritance. Onset usually occurs before the second or third decade of life.Clinical features include round or oval
include columnar parakeratosis.The molecular defect has yet to be identified.AcrokeratoelastoidosisSynonyms include punctate PPK type III, focal acral hyperkeratosis, or acrokeratoelastoidosis of Costa. Acrokeratoelastoidosis is usually sporadic, although familial cases suggest an autosomal dominant pattern of inheritance. Onset usually occurs before the second or third decade of life.Clinical features
parakeratosis.The molecular defect has yet to be identified.AcrokeratoelastoidosisSynonyms include punctate PPK type III, focal acral hyperkeratosis, or acrokeratoelastoidosis of Costa. Acrokeratoelastoidosis is usually sporadic, although familial cases suggest an autosomal dominant pattern of inheritance. Onset usually occurs before the second or third decade of life.Clinical features include round or oval
parakeratosis.The molecular defect has yet to be identified.AcrokeratoelastoidosisSynonyms include punctate PPK type III, focal acral hyperkeratosis, or acrokeratoelastoidosis of Costa. Acrokeratoelastoidosis is usually sporadic, although familial cases suggest an autosomal dominant pattern of inheritance. Onset usually occurs before the second or third decade of life.Clinical features include round or oval