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  • #REDIRECT [[EhlersDanlos syndromes]]
    108 bytes (12 words) - 19:58, 3 February 2024
  • '''Ehlers-Danlos Syndrome''' (''pronunciation: AY-lurz-DAN-lowz'') is a group of inherited disorders ...ndrome is named after two doctors, [[Edvard Ehlers]] and [[Henri-Alexandre Danlos]], who first described it in the late 19th and early 20th centuries.
    2 KB (257 words) - 06:42, 11 February 2024
  • ...d after two dermatologists, Edvard Ehlers from Denmark and Henri-Alexandre Danlos from France) is a group of [[Genetic disorder|genetic disorders]] that prim ...skin, [[Joint hypermobility|hypermobile joints]], and fragile tissues. The syndrome is caused by mutations in genes responsible for the structure, production,
    2 KB (272 words) - 21:53, 14 February 2024

Page text matches

  • '''Ehlers-Danlos Syndrome''' (''pronunciation: AY-lurz-DAN-lowz'') is a group of inherited disorders ...ndrome is named after two doctors, [[Edvard Ehlers]] and [[Henri-Alexandre Danlos]], who first described it in the late 19th and early 20th centuries.
    2 KB (257 words) - 06:42, 11 February 2024
  • ...rfan Syndrome|Marfan syndrome]] and [[Ehlers-Danlos Syndrome|Ehlers-Danlos syndrome]]. ...os syndrome, [[Homocystinuria|homocystinuria]], and [[Beals Syndrome|Beals syndrome]].
    2 KB (290 words) - 04:36, 7 February 2024
  • ...d after two dermatologists, Edvard Ehlers from Denmark and Henri-Alexandre Danlos from France) is a group of [[Genetic disorder|genetic disorders]] that prim ...skin, [[Joint hypermobility|hypermobile joints]], and fragile tissues. The syndrome is caused by mutations in genes responsible for the structure, production,
    2 KB (272 words) - 21:53, 14 February 2024
  • ...[Marfan Syndrome|Marfan syndrome]], [[Ehlers-Danlos Syndrome|Ehlers-Danlos syndrome]], and other [[Connective Tissue Disorder|connective tissue disorders]]. It * [[Marfan Syndrome|Marfan syndrome]]
    2 KB (225 words) - 06:57, 14 February 2024
  • ...ain medical conditions, particularly [[Ehlers-Danlos syndrome]] and [[Down syndrome]]. ...pathologist who first described the sign in the context of [[Ehlers-Danlos syndrome]].
    1 KB (211 words) - 06:02, 8 February 2024
  • == Painful Bruising Syndrome == ...ronunciation: payn-ful broo-zing sin-drohm), also known as [[Ehlers-Danlos Syndrome]] or [[Hematoma]], is a medical condition characterized by the occurrence o
    2 KB (263 words) - 19:52, 7 February 2024
  • ...certain genetic disorders such as [[Marfan syndrome]] and [[Ehlers-Danlos syndrome]]. * [[Marfan syndrome]]
    1 KB (200 words) - 20:41, 12 February 2024
  • ...e [[connective tissues]] in the body. It is also known as '''Ehlers-Danlos syndrome type IX''' or '''X-linked cutis laxa'''. ...l, which is a common feature in individuals with this condition. The term "syndrome" is used to describe a collection of symptoms that often occur together.
    2 KB (279 words) - 02:27, 12 February 2024
  • ...Headache|headache]], [[Neck Pain|neck pain]], [[Horner's Syndrome|Horner's syndrome]], and [[Stroke|stroke]] symptoms such as [[Facial Droop|facial droop]], [[ ...plasia|fibromuscular dysplasia]] or [[Ehlers-Danlos Syndrome|Ehlers-Danlos syndrome]].
    2 KB (272 words) - 04:07, 12 February 2024
  • ...ers. Some of these conditions include [[Marfan syndrome]], [[Ehlers-Danlos syndrome]], and [[osteogenesis imperfecta]]. * [[Marfan syndrome]]
    2 KB (225 words) - 00:41, 9 February 2024
  • ...certain genetic disorders, such as [[Marfan Syndrome]] and [[Ehlers-Danlos Syndrome]]. Individuals with this condition have limbs that are disproportionately l ...dition causing the Dolichostenomelia. For example, individuals with Marfan Syndrome may also experience symptoms such as heart problems, eye abnormalities, and
    2 KB (214 words) - 01:33, 8 February 2024
  • Tracheobronchomegaly, also known as [[Mounier-Kuhn Syndrome]], is a disorder marked by significant enlargement of the trachea and bronc ...ciated with other diseases such as [[Ehlers-Danlos Syndrome]] and [[Marfan Syndrome]].
    2 KB (229 words) - 01:35, 8 February 2024
  • ...mentous laxity''', also known as '''ligament laxity''' or '''hypermobility syndrome''', is a condition where the [[ligament]]s allow an excessive range of move ...joints. Some people with ligamentous laxity may also have [[Ehlers-Danlos syndrome]], a group of disorders that affect the connective tissues supporting the s
    2 KB (208 words) - 17:20, 10 February 2024
  • ...it can also occur as a result of other conditions, such as [[Ehlers-Danlos syndrome]], or as a complication of spinal surgery. * [[Marfan syndrome]]
    2 KB (212 words) - 00:35, 9 February 2024
  • ...otid artery dissection can include [[headache]], [[neck pain]], [[Horner's syndrome]] (a combination of drooping eyelid, constricted pupil, and lack of sweatin ...affect the blood vessels, such as [[Ehlers-Danlos syndrome]] and [[Marfan syndrome]], can also increase the risk of carotid artery dissection.
    2 KB (270 words) - 02:41, 12 February 2024
  • ...s and conditions, such as [[coarctation of the aorta]] and [[Ehlers-Danlos syndrome]]. * [[Ehlers-Danlos Syndrome]]: This is a group of inherited disorders that affect your connective tissu
    2 KB (220 words) - 06:34, 12 February 2024
  • ...factors. Certain diseases, such as [[Marfan Syndrome]] and [[Ehlers-Danlos Syndrome]], can also increase the risk of developing an aneurysm. * [[Marfan Syndrome]]
    2 KB (265 words) - 20:48, 12 February 2024
  • ...certain genetic disorders, such as [[Marfan syndrome]] and [[Ehlers-Danlos syndrome]]. * [[Marfan syndrome]]
    2 KB (251 words) - 23:33, 9 February 2024
  • ...defects in dermatan sulfate can lead to disorders such as [[Ehlers-Danlos syndrome]], a group of inherited disorders that affect the connective tissues suppor * [[Ehlers-Danlos syndrome]]
    1 KB (190 words) - 23:12, 14 February 2024
  • ...certain genetic disorders, such as [[Marfan Syndrome]] and [[Ehlers-Danlos Syndrome]]. * [[Marfan Syndrome]]
    2 KB (256 words) - 17:16, 10 February 2024

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