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Descriptor en español: Síndrome de Isaacs
Descriptor síndrome de Isaacs
Término(s) alternativo(s) miocimia continua
neuromiotonía
neuromiotonía adquirida
pseudomiotonia
Nota de alcance: Trastorno neuromuscular poco frecuente que suele iniciarse al final de la infancia o al inicio de la edad adulta, caracterizado por contracciones musculares diseminadas, intermitentes o contínuas, FASCICULACIONES, hiporreflexia, CALAMBRE MUSCULAR, DEBILIDAD MUSCULAR, HIPERHIDROSIS, TAQUICARDIA, y MIOCIMIA. La participación de los músculos faríngeos y laríngeos puede interferir con el lenguaje y la respiración. La actividad motora contínua persiste durante el sueño y la anestesia general (lo que distingue a esta afección del SÍNDROME DE STIFF-PERSON). Se han refeido formas familiares y adquiridas (primariamente autoimmunitarias). (Ann NY Acad Sci 1998 May 13;841:482-496; Adams et al., Principles of Neurology, 6th ed, p1491)
Descriptor en inglés: Isaacs Syndrome
Descriptor en portugués: Síndrome de Isaacs
Descriptor en francés: Syndrome d'Isaacs-Mertens
Término(s) alternativo(s): Acquired Neuromyotonia
Continuous Muscle Activity Syndrome
Continuous Myokymia
Continuous Myokymias
Gamstorp Wohlfart Syndrome
Gamstorp-Wohlfart Syndrome
Isaac Syndrome
Isaacs Mertens Syndrome
Isaacs Pseudomyotonia Syndrome
Isaacs' Syndrome
Isaacs-Mertens Syndrome
Myokymia, Continuous
Myokymia, Myotonia, Muscle Wasting, And Hyperhidrosis
Myokymias, Continuous
Neuromyotonia
Neuromyotonia, Acquired
Pseudomyotonia
Pseudomyotonia Syndrome of Isaacs
Quantal Squander
Syndrome of Continuous Muscle Activity
Código(s) jeráquico(s): C05.651.392
C10.668.829.425
Identificador Único RDF: https://id.nlm.nih.gov/mesh/D020386
Nota de alcance: A rare neuromuscular disorder with onset usually in late childhood or early adulthood, characterized by intermittent or continuous widespread involuntary muscle contractions; FASCICULATION; hyporeflexia; MUSCLE CRAMP; MUSCLE WEAKNESS; HYPERHIDROSIS; TACHYCARDIA; and MYOKYMIA. Involvement of pharyngeal or laryngeal muscles may interfere with speech and breathing. The continuous motor activity persists during sleep and general anesthesia (distinguishing this condition from STIFF-PERSON SYNDROME). Familial and acquired (primarily autoimmune) forms have been reported. (From Ann NY Acad Sci 1998 May 13;841:482-496; Adams et al., Principles of Neurology, 6th ed, p1491)
Calificadores 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
Indexación anterior: Fasciculation (1995-1999)
Nota Pública de MeSH: 2000; for ISAACS' SYNDROME see FASCICULATION 1995-1999
Nota de historia: 2000; for ISAACS' SYNDROME use FASCICULATION 1995-1999
Identificador de DeCS: 34193
ID del Descriptor: D020386
Documentos indizados en la Biblioteca Virtual de Salud (BVS): Haga clic aquí para acceder a los documentos de la BVS
Fecha de establecimiento: 01/01/2000
Fecha de entrada: 03/11/1999
Fecha de revisión: 17/05/2019
Isaacs Syndrome - Concepto preferido
UI del concepto M0008237
Nota de alcance A rare neuromuscular disorder with onset usually in late childhood or early adulthood, characterized by intermittent or continuous widespread involuntary muscle contractions; FASCICULATION; hyporeflexia; MUSCLE CRAMP; MUSCLE WEAKNESS; HYPERHIDROSIS; TACHYCARDIA; and MYOKYMIA. Involvement of pharyngeal or laryngeal muscles may interfere with speech and breathing. The continuous motor activity persists during sleep and general anesthesia (distinguishing this condition from STIFF-PERSON SYNDROME). Familial and acquired (primarily autoimmune) forms have been reported. (From Ann NY Acad Sci 1998 May 13;841:482-496; Adams et al., Principles of Neurology, 6th ed, p1491)
Término preferido Isaacs Syndrome
Término(s) alternativo(s) Continuous Muscle Activity Syndrome
Continuous Myokymia
Continuous Myokymias
Gamstorp Wohlfart Syndrome
Gamstorp-Wohlfart Syndrome
Isaac Syndrome
Isaacs Mertens Syndrome
Isaacs Pseudomyotonia Syndrome
Isaacs' Syndrome
Isaacs-Mertens Syndrome
Myokymia, Continuous
Myokymia, Myotonia, Muscle Wasting, And Hyperhidrosis
Myokymias, Continuous
Neuromyotonia
Pseudomyotonia Syndrome of Isaacs
Quantal Squander
Syndrome of Continuous Muscle Activity
Acquired Neuromyotonia - Más estrecho
UI del concepto M0335867
Término preferido Acquired Neuromyotonia
Término(s) alternativo(s) Neuromyotonia, Acquired
Pseudomyotonia - Relacionado pero no más amplio ni más estrecho
UI del concepto M000641915
Término preferido Pseudomyotonia



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