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Symptom Checker » Acute Alzheimers-like memory loss » Alzheimers-like memory loss
 

Acute Alzheimers-like memory loss and Alzheimers-like memory loss and Arm symptoms and Epilepsy and Inability to think coherently
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Acute Alzheimers-like memory loss and Alzheimers-like memory loss and Arm symptoms and Epilepsy and Inability to think coherently

  • Acute Alzheimers-like memory loss AND Alzheimers-like memory loss AND Arm symptoms AND Epilepsy AND Inability to think coherently - Causes of All Symptoms
  • Acute Alzheimers-like memory loss OR Alzheimers-like memory loss OR Arm symptoms OR Epilepsy OR Inability to think coherently - 1679 causes

Acute Alzheimers-like memory loss:

Alzheimers-like memory loss:

Arm symptoms:

Epilepsy:

Inability to think coherently:

Results: Causes of Acute Alzheimers-like memory loss AND Alzheimers-like memory loss AND Arm symptoms AND Epilepsy AND Inability to think coherently

Note: Do not use for diagnosis; see limitations of results.

Results: 1679 causes of Acute Alzheimers-like memory loss OR Alzheimers-like memory loss OR Arm symptoms OR Epilepsy OR Inability to think coherently

    1. 18p minus syndrome
     A rare chromosomal disorder where a portion of chromosome 18 is missing which is characterized by mental and growth deficiencies, drooping upper eyelid and prominent ears. The type and severity of symptoms is determined by the amount of genetic material t...more »
    2. 1q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    3. 2-Hydroxyglutaricaciduria
     A rare metabolic disorder characterized by high levels of a certain chemical (2-Hydroxyglutaric) which causes a serious progressive neurological disease and damage to the brain. The features of this disorder are variable and some cases are milder than oth...more »
    4. 22q11.2 deletion syndrome
     A rare genetic disorder caused by the absence of a small portion of genetic material. A small section of chromosome 22 is missing at a location called q11.2. Chromosome 22 is one of 23 pairs of chromosomes that exist in humans....more »
    5. 2q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    6. 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 »
    7. 3-methylglutaconic aciduria, type 1
     A recessively inherited metabolic disorder characterized by methylglutaconic acid in the urine....more »
    8. 3q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 3 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    9. 46,XX chromosome 7 deletion p13
     A chromosomal disorder where a small portion of chromosome 7 is deleted which results in a range of abnormalities....more »
    10. 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 »

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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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