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2,805 Possible Causes for Ehlers Danlos Syndrome

  • Postural Orthostatic Tachycardia Syndrome

    Anesthetic considerations for Ehlers-Danlos syndrome. Anesthesiology. 1980;52:266–269. PubMed CrossRef 6.[springermedizin.de] People who experience Ehlers-Danlos syndrome may also have POTS; joint hyper-mobility is a feature of the most common subtype of Ehlers-Danlos.[disabled-world.com] Numerous other chronic conditions have been associated with POTS (abridged list): Chronic fatigue syndrome Celiac disease Diabetes Ehlers-Danlos Syndrome Lyme disease Fibromyalgia[pedemmorsels.com]

  • Aortic Aneurysm and Dissection

    Heritable syndromic conditions, such as Marfan syndrome, Loeys-Dietz syndrome, and vascular Ehlers-Danlos syndrome, have somewhat overlapping systemic features, but careful[ncbi.nlm.nih.gov] , Ehlers-Danlos syndrome, or Loeys-Dietz syndrome Trauma How Can You Tell if You Have an Aneurysm?[bcm.edu] The most common of these conditions are Marfan syndrome, Loeys-Dietz syndrome ( LDS ), and vascular Ehlers-Danlos syndrome (vEDS).[invitae.com]

  • Thoracic Aortic Aneurysm

    Other risk factors for a thoracic aneurysm include: Changes caused by age Connective tissue disorders such as Marfan or Ehlers-Danlos syndrome Inflammation of the aorta Injury[nlm.nih.gov] Besides Marfan syndrome, Ehlers-Danlos, Loeys-Dietz and Turner syndromes, and other family-related disorders can cause an aortic aneurysm.[mayoclinic.org] Heritable syndromic conditions, such as Marfan syndrome, Loeys-Dietz syndrome, and vascular Ehlers-Danlos syndrome, have somewhat overlapping systemic features, but careful[ncbi.nlm.nih.gov]

  • Connective Tissue Disease

    Ehlers-Danlos Syndromes Ehlers-Danlos Syndromes are a group of genetic disorders that share features such as easy bruising, loose and flexible joints, fragile skin, and weakened[columbiasurgery.org] EhlersDanlos syndrome – defect in the synthesis of collagen (Type I or III) causes progressive deterioration of collagens, with different EDS types affecting different sites[en.wikipedia.org] ) and Ehlers-Danlos syndrome (many types may have loose, fragile skin or loose [hyperextensible] joints depending on type).[medicinenet.com]

  • Aortic Dissection

    BACKGROUND Vascular type of Ehlers-Danlos syndrome (vEDS) is a rare connective tissue disorder associated with a high prevalence rate of aortic dissection (AD).[ncbi.nlm.nih.gov] The Ehlers-Danlos syndromes, rare types.[dx.doi.org] Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome.[ncbi.nlm.nih.gov]

  • Aortic Aneurysm

    Sometimes people with inherited connective tissue disorders, such as Marfan syndrome and Ehlers-Danlos syndrome, get thoracic aortic aneurysms.[cdc.gov] Besides Marfan syndrome, Ehlers-Danlos, Loeys-Dietz and Turner syndromes, and other family-related disorders can cause an aortic aneurysm.[mayoclinic.org] Some inherited connective tissue disorders, such as Marfan syndrome and Ehlers-Danlos syndrome, can also increase your risk for aortic aneurysm.[cdc.gov]

  • Rare Disease with Thoracic Aortic Aneurysm and Aortic Dissection

    Ehlers-Danlos Syndrome People with Ehlers-Danlos Syndrome (EDS) have a defect in their connective tissue, leaving them with fragile skin and unstable joints.[umcvc.org] Ehler-Danlos syndrome The other genetic cause of aortic aneurysm is Ehler-Danlos syndrome.[intechopen.com] Ehlers-Danlos syndrome is another genetic disorder of connective tissue affecting synthesis of collagen.[escardio.org]

  • Cutis Laxa

    syndrome.[ncbi.nlm.nih.gov] 2015 ICD-9-CM Diagnosis Code 756.83 Ehlers-Danlos syndrome 2015 Billable Thru Sept 30/2015 Non-Billable On/After Oct 1/2015 ICD-9-CM 756.83 is a billable medical code that[icd9data.com] syndrome ( Q79.6 ) acquired L57.4 senile L57.4 Dermatorrhexis Q79.6 ICD-10-CM Diagnosis Code Q79.6 Ehlers-Danlos syndrome 2016 2017 2018 2019 Billable/Specific Code POA Exempt[icd10data.com]

  • Orthostatic Intolerance due to NET Deficiency

    Ehlers-Danlos syndrome: A distinct subtype?"[dinet.org] Alan Hakim, Chris O'Callaghan, Inge De Wandele, Lauren Stiles, Alan Pocinki and Peter Rowe, Cardiovascular autonomic dysfunction in EhlersDanlos syndrome—Hypermobile type[doi.org] EhlersDanlos syndrome type III).[doi.org]

  • Keratoglobus

    (keratoglobus) 112 results [Ocular manifestations in Ehlers-Danlos Syndromes: Clinical study of 21 patients].[unboundmedicine.com] Three patients had isolated KGB, 2 were affected with the Ehlers-Danlos syndrome, and the other subject had osteogenesis imperfecta.[ncbi.nlm.nih.gov] The congenital form has been associated with blue sclera in which there is a systemic connective tissue disorder with abnormal collagen synthesis like Ehlers-Danlos syndrome[ncbi.nlm.nih.gov]

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