(Q95.2) Balanced autosomal rearrangement in abnormal individual

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3 714 in individuals diagnosis balanced autosomal rearrangement in abnormal individual confirmed
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1 384 deaths with diagnosis balanced autosomal rearrangement in abnormal individual
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37% mortality rate associated with the disease balanced autosomal rearrangement in abnormal individual

Diagnosis balanced autosomal rearrangement in abnormal individual is diagnosed Women are 51.80% more likely than Men

895

Men receive the diagnosis balanced autosomal rearrangement in abnormal individual

0 (less than 0.1%)

Died from this diagnosis.

100
95
90
85
80
75
70
65
60
55
50
45
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20
15
10
5
0
2 819

Women receive the diagnosis balanced autosomal rearrangement in abnormal individual

1 384 (49.1 %)

Died from this diagnosis.

Risk Group for the Disease balanced autosomal rearrangement in abnormal individual - Men aged 0 and Women aged 10-14

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In Men diagnosis is most often set at age 0-1, 15-19, 65-69
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Less common in men the disease occurs at Age 0-14, 20-64, 70-95+Less common in women the disease occurs at Age 5-9, 15-19, 30-44, 50-59, 65-74, 80-95+
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In Women diagnosis is most often set at age 0-5, 10-14, 20-29, 45-49, 60-64, 75-79

Disease Features balanced autosomal rearrangement in abnormal individual

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Absence or low individual and public risk
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Balanced autosomal rearrangement in abnormal individual - what does this mean

Balanced autosomal rearrangement is a genetic disorder in which there is a rearrangement of genetic material between two chromosomes, resulting in an abnormal individual. this rearrangement can be caused by a number of factors, including chromosomal deletions, duplications, inversions, and translocations. the rearrangement can lead to a variety of symptoms, including physical deformities, developmental delays, and intellectual disabilities.

What happens during the disease - balanced autosomal rearrangement in abnormal individual

Balanced autosomal rearrangement in abnormal individuals is a condition caused by a rearrangement of chromosomal material between two non-homologous chromosomes. this rearrangement can cause a variety of genetic disorders, including developmental delays, physical anomalies, intellectual disability, and other health problems. the rearrangement of chromosomal material can be caused by errors in meiosis or by exposure to environmental factors, such as radiation. the effects of the rearrangement can vary significantly depending on the type and extent of the rearrangement.

Clinical Pattern

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How does a doctor diagnose

  • Physical examination of the individual
  • Medical history review
  • Genetic testing (e.g. karyotyping, FISH, PCR, etc.)
  • Chromosomal microarray analysis
  • DNA sequencing
  • Cytogenetic analysis
  • Imaging studies (e.g. MRI, CT scan, etc.)

Treatment and Medical Assistance

Main Goal: To treat the balanced autosomal rearrangement in an abnormal individual.
  • Identify the underlying cause of the rearrangement.
  • Administer genetic counseling to the individual and their family.
  • Develop a treatment plan based on the individual's medical history and the cause of the rearrangement.
  • Provide appropriate medications, therapies, and lifestyle modifications to manage symptoms.
  • Monitor the individual's progress and adjust the treatment plan as needed.
  • Educate the individual and their family about the condition and how to manage it.
  • Refer the individual to specialists as needed.
  • Provide emotional support and resources to the individual and their family.
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6 Days of Hospitalization Required
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26 Hours Required for Outpatient Treatment

Balanced autosomal rearrangement in abnormal individual - Prevention

The best way to prevent balanced autosomal rearrangement in abnormal individuals is to ensure that all individuals receive comprehensive genetic counseling before and during pregnancy, as well as regular prenatal testing throughout the pregnancy. this will help identify any potential risks associated with the rearrangement and allow for timely intervention if necessary. additionally, it is important to follow up with regular postnatal genetic testing to ensure any abnormalities are detected and managed appropriately.