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Symptom Checker » Bulging fontanelle in neonates » Acute CNS degeneration
 

Bulging fontanelle in neonates and Acute CNS degeneration and Deafness and Strabismus in children
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Bulging fontanelle in neonates and Acute CNS degeneration and Deafness and Strabismus in children

  • Bulging fontanelle in neonates AND Acute CNS degeneration AND Deafness AND Strabismus in children - Causes of All Symptoms
  • Bulging fontanelle in neonates OR Acute CNS degeneration OR Deafness OR Strabismus in children - 983 causes

Bulging fontanelle in neonates:

Acute CNS degeneration:

Deafness:

Strabismus in children:

Results: Causes of Bulging fontanelle in neonates AND Acute CNS degeneration AND Deafness AND Strabismus in children

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

Results: 983 causes of Bulging fontanelle in neonates OR Acute CNS degeneration OR Deafness OR Strabismus in children

    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. 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 »
    3. 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 »
    4. 3-methylglutaconic aciduria, type 4
     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. Type 4 is characterized by symptoms which overlap type 1 and 3....more »
    5. ABCD syndrome
     A rare inherited condition characterized by albinism, deafness, a black lock of hair and intestinal abnormalities....more »
    6. Abidi X-linked mental retardation syndrome
     A rare genetic disorder characterized by a number of physical abnormalities...more »
    7. Abruzzo Erickson syndrome
     A genetic disorder characterized by a combination of features including cleft palate, coloboma and deafness....more »
    8. Acoustic Neurinoma
     A benign tumor of the 8th cranial nerve which lies in the tube connecting the inner ear to the brain....more »
    9. Acoustic neuroma
     A benign tumor of the 8th cranial nerve which lies in the tube connecting the inner ear to the brain....more »
    10. Acrocephalosyndactyly Syndrome type 5
     A rare genetic disorder where some of the skull bones fuse too early which affects the size and shape of the skull and face. Thumb and toe abnormalities are also present. There are three types of Pfeiffer syndrome with varying degrees of severity....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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