Inherited Epidermolysis Bullosa – A Case Report of Several Family Members in Three Generations

L. Vujanović, M. Jovanović, Z. Golušin, Svetlana Kovačić Dukić, Sanja Jakovljević, Milos Nisavic
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Abstract

Abstract Inherited epidermolysis bullosa (IEB) is a genodermatosis transmitted in either autosomal dominant or autosomal recessive manner. The disease is characterized by the development of blisters, erosions, scars, nail dystrophy and scalp abnormalities. Our case report has included four members of one family in three generations with manifested disease. Our 25-year-old female patient presented with a few eroded, crusted, nummular lesions localized on the dorsal plate of interphalangeal joints of fingers, elbow and knee skin, while anonychia was found on her digits. Our youngest patient (her 3.5-year-old son) presented with the lesions in the form of blisters filled with serous fluid, erosions, recent scars and atrophy. Some atrophic scars on the elbow and knee skin were found in our patient′s younger brother, aged 16. The 46-year-old mother of our female patient had nail dystrophy on her hands accompanied by the toenails absence. Pediatric geneticist created the pedigree chart which showed autosomal dominant inheritance pattern with complete expressivity and penetrance. Further diagnostics was not done because the family was not interested.
遗传性大疱性表皮松解症——几代家族成员的一例报告
遗传性大疱性表皮松解症(IEB)是一种常染色体显性或常染色体隐性遗传的遗传性皮肤病。该疾病的特点是水疱,糜烂,疤痕,指甲营养不良和头皮异常的发展。我们的病例报告包括一个家族三代四人的显性疾病。我们25岁的女性患者表现为手指指间关节背板,肘关节和膝盖皮肤上的一些侵蚀,结痂,numular病变,同时在她的手指上发现无名氏。我们最小的患者(她3.5岁的儿子)的病变表现为充满浆液的水疱,糜烂,近期疤痕和萎缩。我们的病人的弟弟,16岁,在肘部和膝盖皮肤上发现了一些萎缩性疤痕。我们的女性患者的母亲46岁,她的手指甲营养不良,并伴有脚趾甲缺失。小儿遗传学家创建的家系图显示常染色体显性遗传模式,具有完全的表达性和外显性。由于家属不感兴趣,没有进行进一步的诊断。
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期刊介绍: Serbian Journal of Dermatology and Venereology is a journal of the Serbian Association of Dermatologists and Venereologists. The journal is published in English, quarterly and intended to provide rapid publication of papers in the field of dermatology and venereology. Manuscripts are welcome from all countries in the following categories: editorials, original studies, review articles, professional articles, case reports, and history of medicine.
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