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MUSCULAR DYSTROPHY, OCULOPHARYNGEAL
Descriptors Found:
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DeCS
Descriptor
English
:
Muscular Dystrophy, Oculopharyngeal
Descriptor
Spanish
:
Distrofia Muscular Oculofaríngea
Descriptor
Portuguese
:
Distrofia Muscular Oculofaríngea
Tree Number:
C05.651.534.500.450
C10.668.491.175.500.450
C16.320.577.450
Definition
English
:
An autosomal dominant hereditary
disease
that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the
eyelids
. Mutations in the gene for POLY(A)-BINDING PROTEIN II have been associated with oculopharyngeal
muscular dystrophy.
Indexing Annotation
English
:
/vet: coord with
MUSCULAR DYSTROPHY
, ANIMAL
See Related
English
:
Poly(A)-Binding Protein II
History Note
English
:
2003; use MUSCULAR DYSTROPHIES 2001-2002
Allowable Qualifiers
English
:
BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
CN
congenital
DI
diagnosis
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology
GE
genetics
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology
PC
prevention & control
PX
psychology
RA
radiography
RI
radionuclide imaging
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
US
ultrasonography
UR
urine
VE
veterinary
VI
virology
Record Number:
37274
Unique Identifier:
D039141
Occurrence in VHL
:
Similar:
DeCS
CID-10
SciELO
LILACS
LIS