Facioscapulohumeral_muscular_dystrophy
Erb-Landouzy-Dejerine syndromeFSHDFSHMDFaciohumeroscapular muscular dystrophyFacioscapulohemeral MDFacioscapulohumeral MDFacioscapulohumeral Muscular DystrophyFacioscapulohumeral dystrophyLandouzy-DejerineLandouzy-Dejerine atrophyLandouzy-Dejerine dystrophyLandouzy-Dejerine dystrophy or atrophyLandouzy-Dejerine muscular dystrophyLandouzy-Dejerine syndromeLandouzy–Dejerine muscular dystrophyMuscular dystrophy, facioscapulohumeralMuscular dystrophy facioscapulohumeral
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ASH1LAcceleron PharmaAphagiaBeevor's signCSRP3CalpainopathyChris CarrinoChromosome 4Coats' diseaseDUX4DiplegiaEden-Lange procedureElectromyographyElectromyoneurographyErb-Landouzy-Dejerine syndromeFRG1FSHFSHDFSHMDFacial weaknessFaciohumeroscapular muscular dystrophyFacioscapulohemeral MDFacioscapulohumeral MDFacioscapulohumeral Muscular DystrophyFacioscapulohumeral dystrophyJamie DurieJaycarJohn E. J. RaskoJoseph Jules DejerineLSMEM2LandouzyLandouzy-DejerineLandouzy-Dejerine atrophyLandouzy-Dejerine dystrophyLandouzy-Dejerine dystrophy or atrophyLandouzy-Dejerine muscular dystrophyLandouzy-Dejerine syndromeLandouzy–Dejerine muscular dystrophyLigand-dependent nuclear receptor-interacting factor 1List of MeSH codes (C05)
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primaryTopic
Facioscapulohumeral_muscular_dystrophy
has abstract
De facioscapulohumerale dystro ...... en, maar dit hoeft zeker niet.
@nl
Distrofia Fascio-escápulo-Umer ...... lidade de vida deste paciente.
@pt
Dystrofia twarzowo-łopatkowo-r ...... awił kolejny opis w 1891 roku.
@pl
La distrofia facio-scapolo-ome ...... polare e degli arti superiori.
@it
La distrofia muscular facioesc ...... strofia muscular que existen.
@es
La dystrophie facio-scapulo-hu ...... is Landouzy et Jules Dejerine.
@fr
الحَثَل العضلي الوجهي الكتفي ا ...... بيق في نقاط تداخل علاجي ممكنة.
@ar
面肩胛肱型肌营养不良症(英語:Facioscapulohum ...... 表明FSHD是最常见的肌肉萎缩症,发病率7/100,000。
@zh
alias
Landouzy–Dejerine muscular dystrophy, FSHMD, FSH
@en
DiseasesDB
eMedicine subject
neuro
@en
eMedicine topic
133
@en
geneReviewsId
geneReviewsName
Facioscapulohumeral muscular dystrophy
@en
ICD10
MedlinePlus
MeSH ID
OMIM id
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Wikipage page ID
page length (characters) of wiki page
Wikipage revision ID
1,026,136,242
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align
right
@en
caption
A diagram showing the muscles ...... e moreso affected than orange.
@en
Drawing of one brother at age ...... oral muscles appear atrophied.
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Photograph of another brother ...... ated, and laterally displaced.
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causes
Genetic
@en
complications
Chronic pain, scoliosis
@en
Rare: respiratory insufficiency, hearing loss, retinal disease
@en
diagnosis
Genetic testing
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differential
Limb-girdle muscular dystrophy , Pompe disease, mitochondrial myopathy, polymyositis
@en
direction
horizontal
@en
DiseasesDB
duration
Lifelong
@en
eMedicineSubj
neuro
@en
eMedicineTopic
frequency
Up to 8,333
@en
GeneReviewsName
Facioscapulohumeral muscular dystrophy
@en
GeneReviewsNBK
NBK1443
@en
header
Two brothers with FSHD followed by Landouzy and Dejerine
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ICD
image
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image size
management
Physical therapy, bracing, reconstructive surgery
@en
medication
Clinical trials ongoing
@en
MedlinePlus
MeshID
D020391
@en
name
Facioscapulohumeral muscular dystrophy
@en
OMIM
onset
9.46728E8
Orphanet
prognosis
Progressive, unaffected life expectancy
@en
pronounce
alt.
@en
risks
Male sex
@en
symptoms
Facial weakness, scapular winging, foot drop
@en
synonyms
Landouzy–Dejerine muscular dystrophy, FSHMD, FSH
@en