Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1998 Mar;30(2):71-81.

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

[Article in German]
Affiliations
  • PMID: 9592693
Review

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

[Article in German]
C Spitz et al. Handchir Mikrochir Plast Chir. 1998 Mar.

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.

PubMed Disclaimer

Similar articles

MeSH terms