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[Epidermolysis bullosa hereditaria dystrophica mutilans Hallopeau-Siemens--a complex problem].

作者信息

Spitz C, Rösslein R

机构信息

Abteilung für Handchirurgie, des Universitäts-Kinderspitals Basel.

出版信息

Handchir Mikrochir Plast Chir. 1998 Mar;30(2):71-81.

PMID:9592693
Abstract

Epidermolysis bullosa hereditaria dystrophica mutilans Hallopeau-Siemens is an autosomal recessive, chronically mutilating disease. Causal therapy is not known. In a five-year-old boy suffering from this disease and having the right hand completely clumped to a fist, syndactyly and contraction release was performed. The wounds healed under the care of the silicone-coated polyamide net dressing Mepitel. Under intensive postoperative physio- and ergotherapeutic care, a major part of his previous hand function could be restored. Complete epithelialization occurred within four weeks. Twelve months after the procedure, the area of the previous lesions was marked by an unexpected mechanical stability. It was very impressive to see the improvement in his psychological well-being and his sense of self-esteem during this period of partial recovery of his hand function.

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