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Symptom Checker » Acute generalized headache in children » Acute mental distress in children
 

Acute generalized headache in children and Acute mental distress in children and Brudzinski's sign and Mental problems
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Acute generalized headache in children and Acute mental distress in children and Brudzinski's sign and Mental problems

  • Acute generalized headache in children AND Acute mental distress in children AND Brudzinski's sign AND Mental problems - Causes of All Symptoms
  • Acute generalized headache in children OR Acute mental distress in children OR Brudzinski's sign OR Mental problems - 3025 causes

Acute generalized headache in children:

Acute mental distress in children:

Brudzinski's sign:

Mental problems:

Results: Causes of Acute generalized headache in children AND Acute mental distress in children AND Brudzinski's sign AND Mental problems

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

Results: 3025 causes of Acute generalized headache in children OR Acute mental distress in children OR Brudzinski's sign OR Mental problems

    1. 10q Partial Trisomy
     A very rare genetic disorder characterized by the duplication of genetic material from the long arm (q) of chromosome 10 - the genetic material occurs three times in body cells instead of the normal two. The type and severity of symptoms may vary consider...more »
    2. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....more »
    3. 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 »
    4. 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 »
    5. 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 »
    6. 2p21 deletion syndrome
     This syndrome is a more severe form hypotonia-cystinuria syndrome as a larger portion of genetic material from chromosome 2p21 is deleted. It is characterized by infant seizures, reduced muscle tone, developmental delay, lactic acidosis and unusual facial...more »
    7. 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 »
    8. 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 »
    9. 3-methylglutaconic aciduria, type V
     A rare genetic disorder where the body's cells are unable to make sufficient energy resulting in an accumulation in the body of 3-methylglutaconic acid....more »
    10. 3C syndrome
     A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name....more »

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  • Warning - Beta version - information may be incorrect (details)
  • Disclaimer - Do not use this information for diagnosis (details)
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