Create issue ticket

3,159 Possible Causes for Muscular Dystrophies

Show results in: Español

  • Patulous Eustachian Tube

    Other often overlooked causes for ET dysfunction include radiation, stroke, and muscular dystrophy.[audiologyonline.com]

  • Osteoporosis

    Duchenne muscular dystrophy (DMD) is an X-linked recessive muscle disease characterized by secondary osteoporosis and increased fractures.[ncbi.nlm.nih.gov] Furthermore, end-stage renal disease (ESRD), hypercalciuria, congestive heart failure, chronic obstructive lung disease, Parkinson's disease, muscular dystrophies, or injury[symptoma.com]

  • Idiopathic Pulmonary Fibrosis

    They position it as a possible breakthrough in a clutch of indications associated with fibrosis, including pancreatic cancer and Duchenne muscular dystrophy.[fiercebiotech.com]

  • Adrenal Insufficiency

    dystrophy.[emedicine.medscape.com] […] also involves the genes for glycerol kinase deficiency and dystrophin, resulting in elevations in serum glycerol (often measured using a triglyceride assay) and Duchenne muscular[emedicine.medscape.com]

  • Oculopharyngeal Muscular Dystrophy

    Oculopharyngeal muscular dystrophy ( OPMD ) is a rare form of muscular dystrophy with symptoms generally starting when an individual is 40 to 50 years old.[en.wikipedia.org] This report describes four cases of ptosis correction in patients with oculopharyngeal muscular dystrophy in one family.[ncbi.nlm.nih.gov] Oculopharyngeal muscular dystrophy is known as a rare automsomal dominant disease.[ncbi.nlm.nih.gov]

  • Mitral Valve Prolapse

    dystrophy Source: National Heart, Lung, and Blood Institute; National Institutes of Health; U.S.[thehearthospitalbaylor.com] dystrophy.[elcaminohospital.org] dystrophy What are the symptoms of MVP?[urmc.rochester.edu]

  • Cardiomyopathy

    Duchenne muscular dystrophy (DMD) is a rare, X-linked condition with progressive muscle weakness and accompanying cardiomyopathy.[jamanetwork.com] Walker-Warburg syndrome (WWS) is a rare autosomal recessive, congenital muscular dystrophy that is associated with brain and eye anomalies.[ncbi.nlm.nih.gov] dystrophy, tardive; Myopathy, proximal, with early respiratory muscle involvement; Cardiomyopathy, dilated, 1G; Muscular dystrophy, limb-girdle, type 2J; Salih myopathy;[centogene.com]

  • Myasthenia Gravis

    dystrophy, amyotrophic lateral sclerosis, and sarcopenia.[ncbi.nlm.nih.gov] More information on Myasthenia Gravis Mayo Clinic The Myasthenia Gravis Association Muscular Dystrophy Association The Myasthenia Gravis Foundation of America[aanem.org] At Johns Hopkins, our Muscular Dystrophy team has an extensive record of managing patients with MG.[hopkinsmedicine.org]

  • Muscular Atrophy

    […] atrophy (SMA) from similar conditions (such as muscular dystrophy).[mda.org] Choline kinase beta gene (CHKB) mutations have been identified in Megaconial Congenital Muscular Dystrophy (MDCMC) patients, a very rare inborn error of metabolism with 21[ncbi.nlm.nih.gov] Splice-switching antisense oligonucleotides (SSOs) are emerging therapeutics with two SSOs recently approved by the FDA for Duchenne muscular dystrophy and spinal muscular[ncbi.nlm.nih.gov]

  • Spinal Muscular Atrophy

    Mutations of the lamin A/C gene have been associated with several diseases such as Emery-Dreifuss muscular dystrophy, dilated cardiomyopathy and Charcot-Marie-Tooth disease[ncbi.nlm.nih.gov] Splice-switching antisense oligonucleotides (SSOs) are emerging therapeutics with two SSOs recently approved by the FDA for Duchenne muscular dystrophy and spinal muscular[ncbi.nlm.nih.gov] General management and care of spinal muscular dystrophy (SMA) patients in the region varies due to heterogeneous health care.[ncbi.nlm.nih.gov]

Further symptoms

Similar symptoms