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Self-improving dystrophic epidermolysis bullosa with a novel heterozygous missense variant in the COL7A1 gene in a Taiwanese family.
Tsai, Yi-Chia; Tu, Wei-Ting; Su, Chun-Lin; Cheng, Yu-Wen; Chi, Pei-Ling; Hsu, Chao-Kai; Chen, Yang-Yi.
Afiliación
  • Tsai YC; Department of General Medicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
  • Tu WT; Department of Dermatology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Su CL; Department of Dermatology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Cheng YW; Graduate Institute of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
  • Chi PL; Department of Neurosurgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.
  • Hsu CK; Department of Dermatology, Huang PH Dermatology and Aesthetics, Kaohsiung, Taiwan.
  • Chen YY; Department of Dermatology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Wound Repair Regen ; 32(4): 511-516, 2024.
Article en En | MEDLINE | ID: mdl-38415502
ABSTRACT
Self-improving dystrophic epidermolysis bullosa (DEB) is a genodermatosis that is inherited autosomal dominantly or recessively, and its clinical symptoms may improve or subside spontaneously. Herein, we report a case of self-improving DEB with COL7A1 p.Gly2025Asp variant. The diagnosis was made through histopathological, electron microscopic examination, and genetic testing. The same variant is also noted on his father, who presents with dystrophic toenails without any blisters. This study highlights that idiopathic nail dystrophy could be linked to congenital or hereditary disease. Furthermore, we conducted a review of the literature on the characteristics of reported cases of self-improving DEB with a personal or family history of nail dystrophy. The results supported our findings that nail dystrophy may be the sole manifestation in some family members. We suggest that individuals suffering from idiopathic nail dystrophy may seek genetic counselling when planning pregnancy to early evaluate the potential risk of hereditary diseases.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Epidermólisis Ampollosa Distrófica / Mutación Missense / Colágeno Tipo VII Límite: Adult / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Wound Repair Regen Asunto de la revista: DERMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Taiwán

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Epidermólisis Ampollosa Distrófica / Mutación Missense / Colágeno Tipo VII Límite: Adult / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Wound Repair Regen Asunto de la revista: DERMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Taiwán