Pesquisa
Descritor em português: Rigidez Muscular Espasmódica
Descritor em inglês: Stiff-Person Syndrome
Descritor em espanhol: Síndrome de la Persona Rígida
Descritor síndrome de la persona rígida
Termo(s) alternativo(s) síndrome de Moersch-Woltmann
síndrome del hombre rígido
Nota de escopo: Afección que se caracteriza por espasmos persistentes (ESPASMOS) con participación de múltiples músculos, principalmente en las extremidades inferiores y tronco. La enfermedad tiende a ocurrir en la cuarta a sexta década de la vida y se presenta con espasmos intermitentes que se hacen continuos. Pequeños estímulos sensoriales, como son los ruidos o un contacto ligero, precipitan espasmos intensos. Los espasmos no se producen durante el sueño y sólo raramente participan los nervios craneales. La respiración puede afectarse en casos avanzados. (Adams et al., Principles of Neurology, 6th ed, p1492; Neurology 1998 Jul;51(1):85-93)
Descritor em francês: Syndrome de l'homme raide
Termo(s) alternativo(s): Congenital Stiff Man Syndrome
Congenital Stiff-Man Syndrome
Congenital Stiff-Man Syndromes
Congenital Stiff-Person Syndrome
Congenital Stiff-Person Syndromes
Familial Hyperekplexia
Familial Hyperekplexias
Hereditary Hyperekplexia
Hereditary Hyperekplexias
Hyperekplexia, Familial
Hyperekplexia, Hereditary
Hyperekplexias, Familial
Hyperekplexias, Hereditary
Moersch Woltmann Syndrome
Moersch-Woltmann Syndrome
Startle Syndrome
Startle Syndromes
Stiff Man Syndrome
Stiff Person Syndrome
Stiff Trunk Syndrome
Stiff-Baby Syndrome
Stiff-Baby Syndromes
Stiff-Man Syndrome
Stiff-Man Syndrome, Congenital
Stiff-Man Syndromes, Congenital
Stiff-Person Syndrome, Congenital
Stiff-Person Syndromes, Congenital
Stiff-Trunk Syndrome
Stiff-Trunk Syndromes
Stiffman Syndrome
Syndrome, Congenital Stiff-Man
Syndrome, Congenital Stiff-Person
Syndrome, Moersch-Woltmann
Syndrome, Startle
Syndrome, Stiff-Baby
Syndrome, Stiff-Man
Syndrome, Stiff-Person
Syndrome, Stiff-Trunk
Syndrome, Stiffman
Syndromes, Congenital Stiff-Man
Syndromes, Congenital Stiff-Person
Syndromes, Startle
Syndromes, Stiff-Baby
Syndromes, Stiff-Trunk
Código(s) hierárquico(s): C10.114.812
C10.228.854.790
C10.668.900
C20.111.258.850
Identificador Único RDF: https://id.nlm.nih.gov/mesh/D016750
Nota de escopo: A condition characterized by persistent spasms (SPASM) involving multiple muscles, primarily in the lower limbs and trunk. The illness tends to occur in the fourth to sixth decade of life, presenting with intermittent spasms that become continuous. Minor sensory stimuli, such as noise and light touch, precipitate severe spasms. Spasms do not occur during sleep and only rarely involve cranial muscles. Respiration may become impaired in advanced cases. (Adams et al., Principles of Neurology, 6th ed, p1492; Neurology 1998 Jul;51(1):85-93)
Qualificadores permitidos: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Indexação Anterior: Autoimmune Diseases (1988-1991)
Central Nervous System Diseases (1986-1991)
Fibromyalgia (1966-1976)
Muscular Diseases (1966-1982)
Neuromuscular Diseases (1972-1991)
Nota MeSH pública: 2000; see STIFF-MAN SYNDROME 1992-1999
Nota histórica: 2000(1992)
Identificador DeCS: 29809
ID do descritor: D016750
Documentos indexados na Biblioteca Virtual em Saúde (BVS): Clique aqui para acessar os documentos da BVS
Data de estabelecimento: 01/01/1992
Data de entrada: 29/04/1991
Data de revisão: 20/01/2016
Stiff-Person Syndrome - Conceito preferido
Identificador do conceito M0025507
Nota de escopo A condition characterized by persistent spasms (SPASM) involving multiple muscles, primarily in the lower limbs and trunk. The illness tends to occur in the fourth to sixth decade of life, presenting with intermittent spasms that become continuous. Minor sensory stimuli, such as noise and light touch, precipitate severe spasms. Spasms do not occur during sleep and only rarely involve cranial muscles. Respiration may become impaired in advanced cases. (Adams et al., Principles of Neurology, 6th ed, p1492; Neurology 1998 Jul;51(1):85-93)
Termo preferido Stiff-Person Syndrome
Termo(s) alternativo(s) Congenital Stiff Man Syndrome
Congenital Stiff-Man Syndrome
Congenital Stiff-Man Syndromes
Congenital Stiff-Person Syndrome
Congenital Stiff-Person Syndromes
Moersch Woltmann Syndrome
Moersch-Woltmann Syndrome
Startle Syndrome
Startle Syndromes
Stiff Man Syndrome
Stiff Person Syndrome
Stiff Trunk Syndrome
Stiff-Baby Syndrome
Stiff-Baby Syndromes
Stiff-Man Syndrome
Stiff-Man Syndrome, Congenital
Stiff-Man Syndromes, Congenital
Stiff-Person Syndrome, Congenital
Stiff-Person Syndromes, Congenital
Stiff-Trunk Syndrome
Stiff-Trunk Syndromes
Stiffman Syndrome
Syndrome, Congenital Stiff-Man
Syndrome, Congenital Stiff-Person
Syndrome, Moersch-Woltmann
Syndrome, Startle
Syndrome, Stiff-Baby
Syndrome, Stiff-Man
Syndrome, Stiff-Person
Syndrome, Stiff-Trunk
Syndrome, Stiffman
Syndromes, Congenital Stiff-Man
Syndromes, Congenital Stiff-Person
Syndromes, Startle
Syndromes, Stiff-Baby
Syndromes, Stiff-Trunk
Familial Hyperekplexia - Mais específico
Identificador do conceito M000612919
Termo preferido Familial Hyperekplexia
Termo(s) alternativo(s) Familial Hyperekplexias
Hyperekplexia, Familial
Hyperekplexias, Familial
Hereditary Hyperekplexia - Mais amplo
Identificador do conceito M000612920
Termo preferido Hereditary Hyperekplexia
Termo(s) alternativo(s) Hereditary Hyperekplexias
Hyperekplexia, Hereditary
Hyperekplexias, Hereditary



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