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Symptom Checker » Bulging fontanelle in neonates » Acute CNS degeneration
 

Bulging fontanelle in neonates and Acute CNS degeneration and Spasms
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Contents
  1. Bulging fontanelle in neonates AND Acute CNS degeneration AND Spasms: Causes of All Symptoms
  2. Bulging fontanelle in neonates OR Acute CNS degeneration OR Spasms: 2126 causes
  3. Bulging fontanelle in neonates: Causes
  4. Bulging fontanelle in neonates: Introduction
  5. Acute CNS degeneration: Causes
  6. Acute CNS degeneration: Introduction
  7. Spasms: 2118 causes
  8. Spasms: Introduction
  9. Bulging fontanelle in neonates and Acute CNS degeneration and Spasms and Abdominal symptoms (2 causes)
  10. Bulging fontanelle in neonates and Acute CNS degeneration and Spasms and Acquired mental impairment (2 causes)
  11. Bulging fontanelle in neonates and Acute CNS degeneration and Spasms and Acute CNS demyelination (2 causes)
  12. Bulging fontanelle in neonates and Acute CNS degeneration and Spasms and Acute confusion in children (2 causes)
  13. Bulging fontanelle in neonates and Acute CNS degeneration and Spasms and Acute confusion in the elderly (2 causes)
  14. Bulging fontanelle in neonates and Acute CNS degeneration and Spasms and Acute deterioration of mental state (2 causes)
  15. Bulging fontanelle in neonates and Acute CNS degeneration and Spasms and Acute disorientation (2 causes)
  16. Bulging fontanelle in neonates and Acute CNS degeneration and Spasms and Altered mental state (2 causes)
  17. Bulging fontanelle in neonates and Acute CNS degeneration and Spasms and Altered vital signs (2 causes)
  18. Bulging fontanelle in neonates and Acute CNS degeneration and Spasms and Behavioral symptoms (2 causes)
  19. Bulging fontanelle in neonates and Acute CNS degeneration and Spasms and MORE SYMPTOMS

Bulging fontanelle in neonates and Acute CNS degeneration and Spasms

  • Bulging fontanelle in neonates AND Acute CNS degeneration AND Spasms - Causes of All Symptoms
  • Bulging fontanelle in neonates OR Acute CNS degeneration OR Spasms - 2126 causes

Bulging fontanelle in neonates:

Acute CNS degeneration:

Spasms:

Results: Causes of Bulging fontanelle in neonates AND Acute CNS degeneration AND Spasms

Results: 2126 causes of Bulging fontanelle in neonates OR Acute CNS degeneration OR Spasms

    1. 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 »
    2. 1q terminal deletion
     A rare chromosomal disorder where the terminal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities....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. 2-Methylbutyric Aciduria
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    5. 2-methylbutyryl-coenzyme A dehydrogenase deficiency
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    6. 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 »
    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-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 »
    10. 3-Hydroxyisobutyric aciduria
     A rare inborn metabolic disorder which causes brain and facial anomalies, seizures and growth problems....more »

    More causes » | Show All 2126 Causes
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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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