(Q95) Balanced rearrangements and structural markers, not elsewhere classified

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3 714 in individuals diagnosis balanced rearrangements and structural markers, not elsewhere classified confirmed
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1 384 deaths with diagnosis balanced rearrangements and structural markers, not elsewhere classified
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37% mortality rate associated with the disease balanced rearrangements and structural markers, not elsewhere classified

Diagnosis balanced rearrangements and structural markers, not elsewhere classified is diagnosed Women are 51.80% more likely than Men

895

Men receive the diagnosis balanced rearrangements and structural markers, not elsewhere classified

0 (less than 0.1%)

Died from this diagnosis.

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2 819

Women receive the diagnosis balanced rearrangements and structural markers, not elsewhere classified

1 384 (49.1 %)

Died from this diagnosis.

Risk Group for the Disease balanced rearrangements and structural markers, not elsewhere classified - 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 rearrangements and structural markers, not elsewhere classified

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Absence or low individual and public risk
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Balanced rearrangements and structural markers, not elsewhere classified - what does this mean

Balanced rearrangements and structural markers, not elsewhere classified, is a genetic disorder that occurs when there is a structural change in the chromosome, such as a deletion, duplication, inversion, or translocation, that does not fit into any other known category. this type of rearrangement can cause a variety of developmental and health problems, depending on the size and location of the rearrangement.

What happens during the disease - balanced rearrangements and structural markers, not elsewhere classified

Balanced rearrangements and structural markers, not elsewhere classified, refer to a group of genetic disorders caused by changes in the structure of chromosomes. these changes can be either deletions, duplications, inversions, or translocations of chromosomal material, and can cause a wide range of clinical symptoms, depending on the size and location of the rearrangement. these disorders can be difficult to diagnose due to the lack of recognizable features, and may require extensive testing to identify the underlying genetic cause.

Clinical Pattern

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How does a doctor diagnose

  • Physical examination
  • Laboratory tests
  • Imaging tests
  • Genetic testing
  • Endoscopy
  • Biopsy

Treatment and Medical Assistance

Main goal of the treatment: To rearrange and structure markers in order to treat the disease.
  • Develop an individualized treatment plan based on the patient's medical history and current condition.
  • Prescribe medications to reduce symptoms and reduce the risk of complications.
  • Provide guidance and support to the patient to help them cope with the disease.
  • Encourage the patient to make lifestyle changes to reduce the risk of further complications.
  • Monitor the patient's progress and adjust the treatment plan as needed.
  • Educate the patient and their family members about the disease and its treatments.
  • Refer the patient to other specialists or therapies as needed.
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6 Days of Hospitalization Required
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26 Hours Required for Outpatient Treatment

Balanced rearrangements and structural markers, not elsewhere classified - Prevention

Balanced rearrangements and structural markers, not elsewhere classified can be prevented through regular health check-ups and lifestyle changes such as eating a balanced diet, exercising regularly, avoiding smoking, and limiting alcohol consumption. additionally, it is important to get vaccinated against any illnesses that could increase the risk of developing this condition.

Specified forms of the disease

(Q95.0) Balanced translocation and insertion in normal individual
(Q95.1) Chromosome inversion in normal individual
(Q95.2) Balanced autosomal rearrangement in abnormal individual
(Q95.3) Balanced sex/autosomal rearrangement in abnormal individual
(Q95.4) Individuals with marker heterochromatin
(Q95.5) Individuals with autosomal fragile site
(Q95.8) Other balanced rearrangements and structural markers
(Q95.9) Balanced rearrangement and structural marker, unspecified