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Birth defects and Brain symptoms and Cheek symptoms and Cognitive impairment and Squint
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Contents
  1. Birth defects AND Brain symptoms AND Cheek symptoms AND Cognitive impairment AND Squint: Causes of All Symptoms
  2. Birth defects OR Brain symptoms OR Cheek symptoms OR Cognitive impairment OR Squint: 5052 causes
  3. Birth defects: 351 causes
  4. Birth defects: Introduction
  5. Brain symptoms: 2682 causes
  6. Brain symptoms: Introduction
  7. Cheek symptoms: 100 causes
  8. Cheek symptoms: Introduction
  9. Cognitive impairment: 3501 causes
  10. Cognitive impairment: Introduction
  11. Squint: 291 causes
  12. Squint: Introduction
  13. Birth defects and Brain symptoms and Cheek symptoms and Cognitive impairment and Squint and Arm symptoms (4 causes)
  14. Birth defects and Brain symptoms and Cheek symptoms and Cognitive impairment and Squint and Back symptoms (4 causes)
  15. Birth defects and Brain symptoms and Cheek symptoms and Cognitive impairment and Squint and Behavioral symptoms (4 causes)
  16. Birth defects and Brain symptoms and Cheek symptoms and Cognitive impairment and Squint and Birth symptoms (4 causes)
  17. Birth defects and Brain symptoms and Cheek symptoms and Cognitive impairment and Squint and Body symptoms (4 causes)
  18. Birth defects and Brain symptoms and Cheek symptoms and Cognitive impairment and Squint and Bone symptoms (4 causes)
  19. Birth defects and Brain symptoms and Cheek symptoms and Cognitive impairment and Squint and Deformity symptoms (4 causes)
  20. Birth defects and Brain symptoms and Cheek symptoms and Cognitive impairment and Squint and Developmental problems (4 causes)
  21. Birth defects and Brain symptoms and Cheek symptoms and Cognitive impairment and Squint and Ear symptoms (4 causes)
  22. Birth defects and Brain symptoms and Cheek symptoms and Cognitive impairment and Squint and Eye symptoms (4 causes)
  23. Birth defects and Brain symptoms and Cheek symptoms and Cognitive impairment and Squint and MORE SYMPTOMS

Birth defects and Brain symptoms and Cheek symptoms and Cognitive impairment and Squint

  • Birth defects AND Brain symptoms AND Cheek symptoms AND Cognitive impairment AND Squint - Causes of All Symptoms
  • Birth defects OR Brain symptoms OR Cheek symptoms OR Cognitive impairment OR Squint - 5052 causes

Birth defects:

Brain symptoms:

Cheek symptoms:

Cognitive impairment:

Squint:

Results: Causes of Birth defects AND Brain symptoms AND Cheek symptoms AND Cognitive impairment AND Squint

    1. Chromosome 15q duplication syndrome
     A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 15. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material....read more »
    2. Chromosome 15q, trisomy
     A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 15. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material....read more »
    3. Chromosome 17p, partial deletion
     A rare chromosomal disorder involving deletion of genetic material from the short arm of chromosome 17. The type and severity of symptoms are determined by the amount and location of the lost genetic material....read more »
    4. Chromosome 8p duplication syndrome
     A rare chromosomal disorder where the short arm (p) of chromosome 8 is duplicated resulting in three copies instead of two. The type and severity of symptoms depends on the location and length of genetic material duplicated....read more »

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Results: 5052 causes of Birth defects OR Brain symptoms OR Cheek symptoms OR Cognitive impairment OR Squint

    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. 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 »
    6. 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 »
    7. 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 »
    8. 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 »
    9. 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 »
    10. 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 »

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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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