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1,713 Possible Causes for Ehlers Danlos Syndrome, Muscular Dystrophy

  • Osteoporosis

    […] and Ehlers-Danlos syndrome (These causes of hereditary secondary osteoporosis each are treated differently. ) What are osteoporosis symptoms and signs?[medicinenet.com] 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] dystrophy Source: National Heart, Lung, and Blood Institute; National Institutes of Health; U.S.[thehearthospitalbaylor.com] Grave’s disease Ehlers-Danlos syndrome Ebstein's anomaly Mitral Valve Prolapse Copyright Nucleus Medical Media, Inc.[uvahealth.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] Some syndromes are also associated with it such as the Ehlers-Danlos syndrome, orofacial dystonia, and the Mar fan syndrome.[ 8 , 14 , 15 ] C LINICAL F EATURES The most common[ncbi.nlm.nih.gov] Diaphragmatic hernia in an 8-year-old with Ehlers-Danlos syndrome. Pediatr Surg Int. 1998; 13 :553–555. [ PubMed ] 4. Finsterbush A, Pogrund H.[ncbi.nlm.nih.gov]

  • Muscular Atrophy

    syndrome (XLPH-EDS).[ncbi.nlm.nih.gov] […] 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]

  • Rhizomelic Chondrodysplasia Punctata Type 1

    ( E34.5- ) congenital adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias attributable to enzyme disorders ( D55.- ) Marfan's syndrome ( Q87.4[icd10data.com] (DM) distrofia muscularmuscular dystrophy Distrofia muscular de cinturaslimb-girdle muscular dystrophy Distrofia Muscular de Duchenne (DMD)Duchenne muscular dystrophy (DMD[lexigene.com] […] specific to newborn ( P70-P74 ) Endocrine, nutritional and metabolic diseases E70-E88 2019 ICD-10-CM Range E70-E88 Metabolic disorders Type 1 Excludes androgen insensitivity syndrome[icd10data.com]

  • Stickler Syndrome Type 3

    […] hypermobile Ehlers Danlos syndrome.[physio-pedia.com] , Congenital muscular dystrophy with primary laminin 2 (merosin) deficiency, Merosin negative congenital muscular dystrophy, LAMA-2 related muscular dystrophy (early and late[orphananesthesia.eu] Ehlers-Danlos syndrome, type III (benign hypermobility syndrome) Major diagnostic criteria for Ehlers-Danlos syndrome, type III (OMIM #130020) are as follows: Joint hypermobility[emedicine.medscape.com]

  • Autosomal Recessive Deafness 46

    (EDS) Ehlers-Danlos-Syndrom, Typ IV (EDS4) Ektodermale Dysplasie (ECTD) Emery-Dreifuss-Muskeldystrophie (EDMD) Epilepsie, Pyridoxin-abhängige (EPD) Epileptische Enzephalopathie[zhma.de] Duchenne Muscular Dystrophy Muscular dystrophy (MD) is a group of muscle diseases that weaken the musculoskeletal system and hamper locomotion.[studyres.com] Repository NIGMS Human Genetic Cell Repository Subcollection Heritable Diseases Muscular Dystrophies CMD Specific Biopsy Source Peripheral vein Cell Type B-Lymphocyte Tissue[catalog.coriell.org]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2A

    Congenital valvular dysplasia Distal myopathy with anterior tibial onset Ehlers-Danlos syndrome with periventricular heterotopia Familial idiopathic steroid-resistant nephrotic[csbg.cnb.csic.es] Limb-girdle muscular dystrophies (LGMDs) are a group of inherited diseases whose genetic etiology has yet to be elucidated.[ncbi.nlm.nih.gov] Limb-girdle muscular dystrophies (LGMDs) are a group of neuromuscular diseases presenting great clinical heterogeneity.[ncbi.nlm.nih.gov]

  • Craniofacial Dysplasia-Osteopenia Syndrome

    See also syndrome, Ehlers-Danlos .[medical-dictionary.thefreedictionary.com] Dystrophies; and complex genetic disorders such as Down syndrome.[books.google.com] Duchenne Muscular Dystrophy June 10, 2018 by Peter Ciszewski Duchenne muscular dystrophy (DMD) is a progressive form of muscular dystrophy that occurs primarily in males,[checkrare.com]

  • Autosomal Recessive Deafness 1B

    […] 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] Haemophilia and Duchenne muscular dystrophy (a severe type of muscular dystrophy) are examples of genetic conditions that are inherited in an X-linked recessive way.[aussiedeafkids.org.au] dystrophy 2 Limb-girdle muscular dystrophy 1B Charcot–Marie–Tooth disease 2B1 LMNB Barraquer–Simons syndrome LEMD3 Buschke–Ollendorff syndrome Osteopoikilosis LBR Pelger–Huet[en.wikipedia.org]

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