A Case of Hereditary Sensory Neuropathy Type II with Acroosteolysis / 대한류마티스학회지
The Journal of the Korean Rheumatism Association
;
: 105-110, 1997.
Artigo
em Coreano
| WPRIM
| ID: wpr-79834
ABSTRACT
The hereditary sensory neuropathy is a very rare disease characterized by prominent sensory loss without corresponding motor involvement, but may be associated with autonomic features. Currently, the disease is divided into five main types and most frequent are Type I and Type II. The type II hereditary sensory neuropathy is characterized by autosomal recessive inheritance, onset in utero or in infancy, loss of touch-pressure sense more than paintemperature sense, and almost total absence of myelinated nerve fibers. In this case, we describe a 23 years old female patient with acroosteolysis and heel ulcer who was diagnosed as hereditary sensory neuropathy type II.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Úlcera
/
Testamentos
/
Calcanhar
/
Neuropatias Hereditárias Sensoriais e Autônomas
/
Acro-Osteólise
/
Doenças Raras
/
Fibras Nervosas Mielinizadas
Limite:
Feminino
/
Humanos
Idioma:
Coreano
Revista:
The Journal of the Korean Rheumatism Association
Ano de publicação:
1997
Tipo de documento:
Artigo
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