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Symptom Checker » Dislocated hip » Joint laxity
 

Dislocated hip and Joint laxity and Reduced muscle tone and Vision distortion
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Contents
  1. Dislocated hip AND Joint laxity AND Reduced muscle tone AND Vision distortion: Causes of All Symptoms
  2. Dislocated hip OR Joint laxity OR Reduced muscle tone OR Vision distortion: 2541 causes
  3. Dislocated hip: 91 causes
  4. Dislocated hip: Introduction
  5. Joint laxity: Causes
  6. Joint laxity: Introduction
  7. Reduced muscle tone: 645 causes
  8. Reduced muscle tone: Introduction
  9. Vision distortion: 1913 causes
  10. Vision distortion: Introduction
  11. Dislocated hip and Joint laxity and Reduced muscle tone and Vision distortion and Artery symptoms (3 causes)
  12. Dislocated hip and Joint laxity and Reduced muscle tone and Vision distortion and Back symptoms (3 causes)
  13. Dislocated hip and Joint laxity and Reduced muscle tone and Vision distortion and Bleeding symptoms (3 causes)
  14. Dislocated hip and Joint laxity and Reduced muscle tone and Vision distortion and Blood clots (3 causes)
  15. Dislocated hip and Joint laxity and Reduced muscle tone and Vision distortion and Blood vessel symptoms (3 causes)
  16. Dislocated hip and Joint laxity and Reduced muscle tone and Vision distortion and Bone symptoms (3 causes)
  17. Dislocated hip and Joint laxity and Reduced muscle tone and Vision distortion and Circulation symptoms (3 causes)
  18. Dislocated hip and Joint laxity and Reduced muscle tone and Vision distortion and Contusion (3 causes)
  19. Dislocated hip and Joint laxity and Reduced muscle tone and Vision distortion and Easy bruising (3 causes)
  20. Dislocated hip and Joint laxity and Reduced muscle tone and Vision distortion and Eye symptoms (3 causes)
  21. Dislocated hip and Joint laxity and Reduced muscle tone and Vision distortion and MORE SYMPTOMS

Results: Causes of Dislocated hip AND Joint laxity AND Reduced muscle tone AND Vision distortion

    1. Ehlers-Danlos syndrome type VI
     A rare genetic connective tissue disorder characterized by lax joints, scoliosis and fragile sclera of the eye - Ehlers Danlos type with predominant ocular abnormalities....read more »
    2. Ehlers-Danlos syndrome, 6B
     A rare genetic connective tissue disorder characterized by lax joints, scoliosis and fragile sclera of the eye - Ehlers Danlos type with predominant ocular abnormalities but lysyl-hydroxylase activity is normal1....read more »
    3. Ehlers-Danlos syndrome, kyphoscoliosis type
     A rare genetic connective tissue disorder caused by deficiency of the lysyl hydroxylase enzyme and is characterized by progressive scoliosis and muscle weakness and fragile sclera - previously known as EDS type 6....read more »

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Results: 2541 causes of Dislocated hip OR Joint laxity OR Reduced muscle tone OR Vision distortion

    11. 3 alpha methylglutaconicaciduria, type 3
     A rare genetic condition where a gene mutation prevents the production of certain protein which leads to a build-up of an acid (3-methylglutaconic acid) which can have a negative impact on the body. The condition is characterized mainly by damage to the o...more »
    12. 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Sympt...more »
    13. 3-alpha-Hydroxyacyl-CoA Dehydrogenase Deficiency
     A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activit...more »
    14. 3-alpha-hydroxyacyl-coenzyme A dehydrogenase deficiency
     A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activit...more »
    15. 3-alpha-hydroxyisobutyryl-CoA hydrolase deficiency
     A metabolic disorder involving an enzyme deficiency which causes symptoms such as degeneration of the nervous system. The other features of the disorder are somewhat variable....more »
    16. 3C syndrome
     A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name....more »
    17. 47,XXX syndrome
     A genetic condition where females have an extra X chromosome in each of their cells. Normally female cells have two X chromosomes. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asymptomati...more »
    18. 49,XXXXY syndrome
     A rare sex chromosome abnormality where there are three extra copies of the X chromosome....more »
    19. 4p16.3 deletion
     A rare genetic disorder where a portion of chromosome 4 is deleted at a location called 16.3. The condition is characterized by malformations in most parts of the body as the deletion affects growth and development of the fetus....more »
    20. Abetalipoproteinemia
     A rare disorder involving abnormalities in fat metabolism. The resulting insufficiency of fats and vitamins affect the normal development and function of the body....more »

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Notes About Causes

  • Warning - Beta version - information may be incorrect (details)
  • Disclaimer - Do not use this information for diagnosis (details)
  • Important - See your doctor - Only a doctor can give an accurate diagnosis (details)
 

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