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.

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