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1,488 Possible Causes for Ehlers Danlos Syndrome, Muscular Dystrophy

  • Osteoporosis

    […] thalassemia, leukemia, lymphoma, hemophilia , sickle cell disease , systemic mastocytosis Genetic disorders - Cystic fibrosis , osteogenesis imperfecta , homocystinuria , Ehlers-Danlos[web.archive.org] Abstract 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]

  • Mitral Valve Prolapse

    MVP may also occur in patients suffering from connective tissue disorders like Marfan's syndrome and Ehlers Danlos syndrome.[symptoma.com] Mitral valve prolapse can run in families and may be linked to several other conditions, such as: Marfan syndrome Ehlers-Danlos syndrome Ebstein's anomaly Muscular dystrophy[mayoclinic.com] dystrophy Source: National Heart, Lung, and Blood Institute; National Institutes of Health; U.S.[thehearthospitalbaylor.com]

  • Joint Dislocation

    Others, such as those with Ehlers-Danlos syndrome or Marfan syndrome, have additional problems such as heart valve or eye abnormalities.[sharecare.com]

  • Retinal Detachment

    […] metamorphopsia ; photocoagulation ; lattice degeneration of the retina ; retinal break ; retinal dialysis ; central serous retinopathy ; retinopathy of prematurity ; striae retinae ; Ehlers-Danlos[medical-dictionary.thefreedictionary.com] syndrome ; Marfan's syndrome ; Stickler's syndrome ; ultrasonography ; familial exudative vitreoretinopathy ; vitreous detachment . exudative retinal detachment d.[medical-dictionary.thefreedictionary.com]

  • Exostoses - Anetodermia - Brachydactyly Type E Syndrome

    […] dominant Ehlers-Danlos syndrome type 5 Ehlers-Danlos syndrome type 6 Ehlers-Danlos syndrome type 7A Ehlers-Danlos syndrome type 7B Ehlers-Danlos syndrome type 7C Ehlers-danlos[bioreference.net] dystrophy, dominant type * Emery-Dreifuss muscular dystrophy, X-linked * Emery-Dreifuss muscular dystrophy * Emetophobia * Emphysema, congenital lobar * Emphysema * Emphysema-penoscrotal[en.academic.ru] dystrophy, dominant type Emery-Dreifuss muscular dystrophy, X-linked Emery-Dreifuss muscular dystrophy Emetophobia Emphysema, congenital lobar Emphysema Emphysema-penoscrotal[ssf.f15ijp.com]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    The Ehlers-Danlos syndrome, a disorder with many faces. Clin Genet 2012; 82: 1-11. Duthie G, Singh M, Jester I.[sites.uclouvain.be] dystrophy type 2B Limb-Girdle Muscular Dystrophy type 2C Limb-Girdle Muscular Dystrophy type 2D Limb-Girdle Muscular Dystrophy type 2E Limb-Girdle Muscular Dystrophy, Type[babygene.co.il] […] heterotopia POMGNT1 Muscular dystrophy-dystroglycanopathy POMT1 Muscular dystrophy-dystroglycanopathy POMT2 Muscular dystrophy-dystroglycanopathy RELN Epilepsy, familial temporal[genda.com.ar]

  • Congenital Muscular Dystrophy Type Ullrich

    […] dysplasia (see also C2/11 ) COL3 : EhlersDanlos syndrome, types 3 & 4 Sack–Barabas syndrome COL4 : Alport syndrome COL5 : EhlersDanlos syndrome, types 1 & 2 COL6 : Bethlem[en.wikipedia.org] OBJECTIVES: To describe genetic and clinical features of Ullrich congenital muscular dystrophy (UCMD), and to report the case of a patient diagnosed with UCMD after an exhaustive[ncbi.nlm.nih.gov] It is one of the most common forms of congenital muscular dystrophy (CMD).[musculardystrophyuk.org]

  • Neonatal Hypotonia

    […] and Ehlers-Danlos syndrome.[birthinjurylawyernetwork.com] The genetic differential diagnosis is broad, encompassing primary muscular dystrophies, chromosome abnormalities, neuropathies, and inborn errors of metabolism.[ncbi.nlm.nih.gov] The most common muscular dystrophy in children is Duchene muscular dystrophy.[neuropathology-web.org]

  • Bethlem Myopathy

    […] dysplasia, Strudwick type Kniest dysplasia (see also C2/11 ) COL3 : EhlersDanlos syndrome, types 3 & 4 Sack–Barabas syndrome COL4 : Alport syndrome COL5 : EhlersDanlos[en.wikipedia.org] ; myotonic dystrophy types 1 and 2; and distal muscular dystrophies.[books.google.com] […] grows to adulthood. [1] References External links Image at wustl.edu Diseases of collagen, laminin and other scleroproteins Collagen disease COL1 : Osteogenesis imperfecta EhlersDanlos[ipfs.io]

  • Colobomatous Microphthalmia - Rhizomelic Dysplasia Syndrome

    Dysplastic Form Ehlers-Danlos Syndrome, Type I Ehlers-Danlos Syndrome, Type II Ehlers-Danlos Syndrome, Type IV Ehlers-Danlos Syndrome, Type VI-A Ehlers-Danlos Syndrome, Type[sequencing.com] B, 5 Muscular Dystrophy, Congenital, 1c Muscular Dystrophy, Congenital, Fkrp-Related MDDGB5 MDC1C 606612 Genetic Test Registry Muscular Dystrophy-Dystroglycanopathy (Congenital[ukgtn.nhs.uk] […] imperfecta type 1, Osteogenesis imperfecta type 2, Osteogenesis imperfecta type 3, Osteogenesis imperfecta type 4 COL3A1 Ehlers-Danlos syndrome COL5A1 Ehlers-Danlos syndrome[genda.com.ar]

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