Acro-osteolysis with hereditary sensory ulcero-mutilating neuropathy. Apropos of an atypical case
Carabelli, A.; Ruggeri, R.; Pessina, R.; Cerri, D.; Bertani, E.
Giornale Italiano di Dermatologia e Venereologia Organo Ufficiale Societa Italiana di Dermatologia e Sifilografia 124(11-12): 525-528
1989
ISSN/ISBN: 0392-0488 PMID: 2638645 Document Number: 334194
The authors report an acroosteolysis case with sensory radicular ulcero-mutilating neuropathy. The differential diagnosis are discussed and the case is presented as an intermediate form between the congenital sensory neuropathy, type II, according to Otha classification, and the non-progressive, sporadical sensory neuropathy.