Clinical and functional outcomes of hand surgery for recessive dystrophic epidermolysis bullosa.

 0 Người đánh giá. Xếp hạng trung bình 0

Tác giả: Abdulkadir Calavul, Hakan Cici, Ali İhsan Kılıç, Hakan Zeybek

Ngôn ngữ: eng

Ký hiệu phân loại: 618.17 *Functional and systemic disorders

Thông tin xuất bản: England : The Journal of hand surgery, European volume , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 658903

Recessive dystrophic epidermolysis bullosa causes blistering and scarring of the hands, resulting in contractures fused web spaces and altered function. The aim of this study was to present the short- and mid-term clinical and functional results of a large case series of patients who underwent surgery for recessive dystrophic epidermolysis bullosa-related pseudosyndactyly. The study included 75 hands in 39 children (21 boys, 18 girls) with a mean age of 8 years (range, 4-15) and minimum follow-up of 1 year. Children were assessed with the Birmingham Epidermolysis Bullosa Severity Score Sheet and the ABILHAND-Kids questionnaire before operation and at final follow-up. There were varying degrees of recurrent scarring in all the hands by 24 months after operation. The ABILHAND-Kids questionnaire showed a significant improvement in ability to perform 17 of 21 tasks. In conclusion, despite recurrence that may develop in the short and mid term, surgical release can provide significant improvements in hand function.
Tạo bộ sưu tập với mã QR

THƯ VIỆN - TRƯỜNG ĐẠI HỌC CÔNG NGHỆ TP.HCM

ĐT: (028) 36225755 | Email: tt.thuvien@hutech.edu.vn

Copyright @2024 THƯ VIỆN HUTECH