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Epidermodysplasia verruciformis: report of two patientswith autosomal dominant inheritance

机译:表皮划分性Plasia Verruciformis:两种患者的常染色体显性遗传报告

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Epidermodysplasia verruciformis is a raregenodermatosis associated with mutations in theEVER1/TMC6 and EVER2/TMC8 genes. The inheritanceis considered to be autosomal recessive, but reportssuggesting an autosomal dominant inheritanceindicate disease genetic heterogeneity. Its onsetoccurs in early childhood and presents as acombination of pityriasis versicolor-like, flat wart-likeand seborrheic keratosis-like lesions, with a potentialfor malignant transformation, mainly squamous cellcarcinoma.
机译:表皮细胞增殖率为Verruciformis是一种稀有生命形式化,其与100 / TMC6和EVER2 / TMC8基因的突变相关。继承被认为是常染色体隐性的,但报告术语常染色体显性遗传性遗传疾病遗传异质性。其早期儿童的遗传疾病,并作为敏感的术语术语,血液曲线般的疣状角膜症状病变,具有潜在的恶性转化,主要是鳞状细胞癌。

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