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Results 1 - 10 of 17 for Genetic Brain Disorders
  1. Mitochondrial DNA 
    ... eye to the brain (the optic nerve). Additional genetic and environmental factors ... a progressive brain disorder that usually appears in infancy or early childhood. ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  2. Chromosome 14 
    ... of copies of chromosome 14. A deletion of genetic material from part of the long (q) arm of chromosome 14 can cause FOXG1 syndrome, which is a rare disorder characterized by impaired development and structural brain abnormalities. The region of chromosome 14 that is ...
    https://medlineplus.gov/genetics/chromosome/14 - Genetics
  3. Chromosome 5 
    ... unclear why eosinophils are preferentially affected by this genetic change. More ... near the center of the brain. In each case, the affected individual had extra ...
    https://medlineplus.gov/genetics/chromosome/5 - Genetics
  4. Chromosome 3 
    ... on each chromosome is an active area of genetic research. Because researchers use different approaches to predict ... no associated health problems. It is possible that genetic changes outside the 3q29 region can influence the ...
    https://medlineplus.gov/genetics/chromosome/3 - Genetics
  5. X chromosome 
    ... on each chromosome is an active area of genetic research. Because researchers use different approaches to predict ... condition is caused by an abnormal exchange of genetic material between chromosomes (translocation). This exchange occurs as ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
  6. Chromosome 2 
    ... on each chromosome is an active area of genetic research. Because researchers use different approaches to predict ... deletion syndrome is caused by a deletion of genetic material near the end of the long (q) ...
    https://medlineplus.gov/genetics/chromosome/2 - Genetics
  7. Chromosome 9 
    ... on each chromosome is an active area of genetic research. Because researchers use different approaches to predict ... physical abnormalities, and the characteristic features of a genetic condition called Gorlin syndrome (also known as nevoid ...
    https://medlineplus.gov/genetics/chromosome/9 - Genetics
  8. Chromosome 8 
    ... on each chromosome is an active area of genetic research. Because researchers use different approaches to predict ... number of copies of chromosome 8. Translocations of genetic material between chromosome 8 and other chromosomes can ...
    https://medlineplus.gov/genetics/chromosome/8 - Genetics
  9. Chromosome 11 
    ... on each chromosome is an active area of genetic research. Because researchers use different approaches to predict ... of Beckwith-Wiedemann syndrome are caused by a genetic change known as paternal uniparental disomy (UPD). Paternal ...
    https://medlineplus.gov/genetics/chromosome/11 - Genetics
  10. Chromosome 17 
    ... on each chromosome is an active area of genetic research. Because researchers use different approaches to predict ... intellectual or physical problems, researchers suspect that additional genetic factors may influence whether a person has signs ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
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