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(Q97.9) Sex chromosome abnormality, female phenotype, unspecified
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4 436 in individuals diagnosis sex chromosome abnormality, female phenotype, unspecified confirmed
620 deaths with diagnosis sex chromosome abnormality, female phenotype, unspecified
14% mortality rate associated with the disease sex chromosome abnormality, female phenotype, unspecified
Diagnosis sex chromosome abnormality, female phenotype, unspecified is diagnosed Prevalent in Women Only
0
Men receive the diagnosis sex chromosome abnormality, female phenotype, unspecified
0 (No mortality)Died from this diagnosis.
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4 436
Women receive the diagnosis sex chromosome abnormality, female phenotype, unspecified
620 (14.0 %)Died from this diagnosis.
Risk Group for the Disease sex chromosome abnormality, female phenotype, unspecified - Men aged 0 and Women aged 15-19
No Cases of the Disease Sex chromosome abnormality, female phenotype, unspecified identified in Men
Less common in men the disease occurs at Age 0-95+Less common in women the disease occurs at Age 5-9, 30-39, 55-95+
In Women diagnosis is most often set at age 0-5, 10-29, 40-54
Disease Features sex chromosome abnormality, female phenotype, unspecified
Absence or low individual and public risk
Sex chromosome abnormality, female phenotype, unspecified - what does this mean
Sex chromosome abnormality, female phenotype, unspecified occurs when an individual has an atypical number or arrangement of sex chromosomes, resulting in a female phenotype but the exact abnormality is unknown.
What happens during the disease - sex chromosome abnormality, female phenotype, unspecified
Sex chromosome abnormality, female phenotype, unspecified is a condition in which the female phenotype is present due to an abnormality in the sex chromosomes, but the exact abnormality is unknown. this is most commonly caused by a chromosomal rearrangement, such as a translocation, in which the x and y chromosomes have exchanged pieces of dna, or a deletion or duplication of a portion of the x chromosome. in some cases, the abnormality may also be due to a mutation in a gene that is related to sex determination.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Complete physical exam
- Chromosomal analysis (karyotype)
- Chromosome microarray
- Molecular genetic testing
- Hormonal testing
- Ultrasound imaging
- MRI imaging
Treatment and Medical Assistance
Main goal: To treat the sex chromosome abnormality, female phenotype, unspecified.
- Consult a genetic counselor to discuss the diagnosis and treatment options.
- Undergo genetic testing to determine the exact cause of the abnormality.
- Receive hormone therapy to regulate hormones.
- Receive counseling to help cope with the diagnosis.
- Undergo fertility treatments to increase the chances of having a successful pregnancy.
- Undergo surgery to correct any physical abnormalities.
- Participate in support groups to connect with others with similar diagnoses.
7 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Sex chromosome abnormality, female phenotype, unspecified - Prevention
Prevention of sex chromosome abnormality, female phenotype, unspecified involves genetic counseling for couples planning to have children, to assess the risk of having a child with this condition. it is also important to follow recommended screening guidelines for pregnant women, such as amniocentesis, to detect the presence of this condition in the fetus.