opmd | Oculopharyngeal Muscular Dystrophy - GeneReviews®

Keyword	CPC	PCC	Volume	Score	Length of keyword
opmd	0.74	0.3	857	23	4

Keyword	CPC	PCC	Volume	Score
opmd	1.93	0.4	6168	73
opmd diagnosis	0.91	0.4	2569	10
opm diva	0.81	0.3	132	34
opmd army	0.69	0.4	515	91
opmd treatment	1.81	0.1	4034	61
opmdatabreach.com	0.27	0.8	99	76
opmd nl	1.1	0.3	4866	11
opmd disease	1.05	0.3	7965	52
opmd genetic testing	1.1	0.1	433	2
opmdc	0.25	0.8	8268	30
opwdd	1.23	0.1	9597	18
opmd hrc	1.98	0.8	6647	55
opmd association	0.15	0.5	6553	34
opmd medical abbreviation	1.15	0.7	5550	7
opmd genereviews	0.41	1	6033	79
opmd clinical trials	1.21	0.9	6999	98

Search Results related to opmd on Search Engine

Oculopharyngeal Muscular Dystrophy - GeneReviews® - NCBI …
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK1126/

WEBMar 8, 2001 · Oculopharyngeal muscular dystrophy (OPMD) is characterized by ptosis and dysphagia due to selective involvement of the muscles of the eyelids and pharynx, respectively. Early manifestations of dysphagia include increased time needed to consume a meal and an acquired avoidance of dry foods.

DA: 35 PA: 64 MOZ Rank: 85

Oculopharyngeal Muscular Dystrophy (OPMD) - Diseases
mda.org

https://www.mda.org/disease/oculopharyngeal-muscular-dystrophy

WEBWhat is oculopharyngeal muscular dystrophy (OPMD)? OPMD is a rare, slowly progressive myopathy that is characterized by weakness of the eyelids (ocular) and throat (pharyngeal) muscles. Additionally, OPMD can be associated with proximal (near the body midline) and distal (limb) muscle weakness.

DA: 56 PA: 8 MOZ Rank: 65

Recent Progress in Oculopharyngeal Muscular Dystrophy - PMC
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036457/

WEBMar 29, 2021 · Oculopharyngeal muscular dystrophy (OPMD) is a late-onset intractable myopathy, characterized by slowly progressive ptosis, dysphagia, and proximal limb weakness.

DA: 70 PA: 36 MOZ Rank: 12

Oculopharyngeal Muscular Dystrophy - Symptoms, Causes, …
rarediseases.org

https://rarediseases.org/rare-diseases/oculopharyngeal-muscular-dystrophy/

WEBNov 1, 2017 · Oculopharyngeal muscular dystrophy (OPMD) is a rare genetic muscle disorder with onset during adulthood most often between 40 and 60 years of age. OPMD is characterized by slowly progressive muscle disease (myopathy) affecting the muscles of the upper eyelids and the throat.

DA: 68 PA: 39 MOZ Rank: 74

Oculopharyngeal Muscular Dystrophy - Cleveland Clinic
clevelandclinic.org

https://my.clevelandclinic.org/health/diseases/24078-oculopharyngeal-muscular-dystrophy

WEBOculopharyngeal muscular dystrophy (OPMD) is a rare genetic disease that leads to muscle weakness. You usually develop symptoms in adulthood, around age 40 or 50, even though you’re born with the gene change that causes OPMD. The symptoms of OPMD are progressive, meaning they worsen over time.

DA: 78 PA: 89 MOZ Rank: 95

Oculopharyngeal Muscular Dystrophy (OPMD) | Cedars-Sinai
cedars-sinai.org

https://www.cedars-sinai.org/health-library/diseases-and-conditions/o/oculopharyngeal-muscular-dystrophy-opmd.html

WEBOPMD is a rare genetic condition that causes weakness in the muscles around the upper eyelid and throat. OPMD affects both men and women, usually first appearing in people after 40 years of age. The first symptoms are eyelid drooping and trouble swallowing.

DA: 33 PA: 17 MOZ Rank: 39

Oculopharyngeal muscular dystrophy - Genetic and Rare …
nih.gov

https://rarediseases.info.nih.gov/diseases/7245/oculopharyngeal-muscular-dystrophy/

WEBOculopharyngeal muscular dystrophy (OPMD) is a genetic disorder characterized by slowly progressing muscle disease (myopathy) affecting the muscles of the upper eyelids and the throat. Symptoms may include: eyelid drooping (ptosis), arm and leg weakness, and difficulty swallowing (dysphagia).

DA: 34 PA: 61 MOZ Rank: 27

Oculopharyngeal muscular dystrophy - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Oculopharyngeal_muscular_dystrophy

WEBOculopharyngeal muscular dystrophy (OPMD) is a rare form of muscular dystrophy with symptoms generally starting when an individual is 40 to 50 years old. It can be autosomal dominant neuromuscular disease or autosomal recessive. The most common inheritance of OPMD is autosomal dominant, which means only one copy of the mutated …

DA: 20 PA: 76 MOZ Rank: 75

OPMD Association – Be a part of the cure!
opmd.org

https://opmd.org/

WEBWhat is OPMD. OPMD is a rare, genetic, degenerative disease affecting adults with symptom onset beginning between 40-50 years. Many have the following symptoms: Impaired Vision. Difficulty Swallowing. Lower Body Weakness. Speaking Difficulty. Facial Muscle Weakness. Upper Body Weakness. Learn More. Video courtesy of Dr. Anita H. …

DA: 46 PA: 34 MOZ Rank: 61

Oculopharyngeal Muscular Dystrophy - EyeWiki
aao.org

https://eyewiki.aao.org/Oculopharyngeal_Muscular_Dystrophy

WEBOPMD is typically a late-onset genetic autosomal dominantly inherited disease of skeletal muscles. OPMD primarily involves the extra ocular muscles (oculo-) and the pharynx (-pharyngeal) but often involves the proximal muscles of the extremities as well. It is associated with progressive blepharoptosis (ptosis) and dysphagia.

DA: 16 PA: 55 MOZ Rank: 87