Search
Descriptor English: Myopathy, Central Core
Descriptor Spanish: Miopatía del Núcleo Central
Descriptor miopatía de cuerpos centrales
Entry term(s) síndrome de Shy-Magee
Scope note: Afección miopática congénita hereditaria caracterizada por debilidad e hipotonía en la lactancia y retraso del desarrollo motor. La biopsia muscular revela condensación de las miofibrillas y material miofibrilar en la porción central de cada fibra muscular. (Adams et al., Principles of Neurology, 6th ed, p1452)
Descriptor Portuguese: Miopatia da Parte Central
Descriptor French: Myopathie à axe central
Entry term(s): Central Core Disease
Central Core Disease of Muscle
Central Core Diseases
Central Core Myopathies
Central Core Myopathy
Myopathies, Central Core
Shy Magee Syndrome
Shy-Magee Syndrome
Syndrome, Shy-Magee
Tree number(s): C05.651.575.300
C10.668.491.550.300
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D020512
Scope note: An inherited congenital myopathic condition characterized by weakness and hypotonia in infancy and delayed motor development. Muscle biopsy reveals a condensation of myofibrils and myofibrillar material in the central portion of each muscle fiber. (Adams et al., Principles of Neurology, 6th ed, p1452)
Allowable Qualifiers: 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
Previous Indexing: Muscles/enzymology (1963-1999)
Muscular Atrophy (1963-1999)
Public MeSH Note: 2000; for CENTRAL CORE DISEASE & SHY-MAGEE SYNDROME see NEMALINE MYOPATHY 1994-1999
History Note: 2000; for CENTRAL CORE DISEASE & SHY-MAGEE SYNDROME use NEMALINE MYOPATHY 1994-1999
DeCS ID: 34195
Unique ID: D020512
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2000/01/01
Date of Entry: 1999/11/03
Revision Date: 2013/07/08
Myopathy, Central Core - Preferred
Concept UI M0328271
Scope note An inherited congenital myopathic condition characterized by weakness and hypotonia in infancy and delayed motor development. Muscle biopsy reveals a condensation of myofibrils and myofibrillar material in the central portion of each muscle fiber. (Adams et al., Principles of Neurology, 6th ed, p1452)
Preferred term Myopathy, Central Core
Entry term(s) Central Core Disease
Central Core Disease of Muscle
Central Core Diseases
Central Core Myopathies
Central Core Myopathy
Myopathies, Central Core
Shy Magee Syndrome
Shy-Magee Syndrome
Syndrome, Shy-Magee



We want your feedback on the new DeCS / MeSH website

We invite you to complete a survey that will take no more than 3 minutes.

Go to survey