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(Q92.7) Triploidy and polyploidy
More details coming soon
6 330 in individuals diagnosis triploidy and polyploidy confirmed
3 107 deaths with diagnosis triploidy and polyploidy
49% mortality rate associated with the disease triploidy and polyploidy
Diagnosis triploidy and polyploidy is diagnosed Women are 46.76% more likely than Men
1 685
Men receive the diagnosis triploidy and polyploidy
1 969 (116.9 %)Died from this diagnosis.
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4 645
Women receive the diagnosis triploidy and polyploidy
1 138 (24.5 %)Died from this diagnosis.
Risk Group for the Disease triploidy and polyploidy - Men and Women aged 0
In Men diagnosis is most often set at age 0-9
Less common in men the disease occurs at Age 10-95+Less common in women the disease occurs at Age 5-9, 20-24, 40-95+
In Women diagnosis is most often set at age 0-5, 10-19, 25-39
Disease Features triploidy and polyploidy
Absence or low individual and public risk
Triploidy and polyploidy - what does this mean
Triploidy and polyploidy are chromosomal abnormalities that occur when the fetus has an extra set of chromosomes, resulting in 69 or more chromosomes instead of the normal 46. this can be caused by an error during cell division or by an extra set of chromosomes from the father or mother. triploidy is the presence of three sets of chromosomes, while polyploidy is the presence of more than three sets of chromosomes. these chromosomal abnormalities can lead to serious birth defects and may be incompatible with life.
What happens during the disease - triploidy and polyploidy
Triploidy and polyploidy are chromosomal conditions caused by an abnormal number of chromosomes in the cells. this can occur when the egg or sperm cells involved in reproduction contain an extra set of chromosomes, or when there is an error in cell division during the early stages of development. this can lead to a wide range of physical and mental disabilities, including birth defects, physical abnormalities, intellectual disabilities, and even death.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Evaluation of family history and physical examination
- Ultrasonography
- Chromosomal analysis
- Fluorescent in situ hybridization (FISH)
- Array comparative genomic hybridization (CGH)
- Karyotyping
- Polymerase chain reaction (PCR)
- Molecular genetic testing
Treatment and Medical Assistance
Main Goal: To reduce the physical abnormalities associated with triploidy and polyploidy.
- Genetic counseling to understand the risks associated with the condition
- Regular ultrasound scans to monitor the development of the baby
- Regular fetal echocardiograms to monitor the baby’s heart
- Regular amniocentesis to monitor the baby’s chromosomes
- Maternal and fetal monitoring to detect any abnormalities
- Early delivery in some cases to prevent any further complications
- Conducting prenatal surgeries to correct any physical abnormalities
- Postnatal surgeries to correct any physical abnormalities
- Physical and occupational therapy to help with any physical disabilities
- Speech and language therapy to help with any speech and language delays
- Behavioral therapy to help with any behavioral issues
13 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Triploidy and polyploidy - Prevention
Triploidy and polyploidy are chromosomal abnormalities that can be prevented through pre-implantation genetic testing of embryos prior to in vitro fertilization. this testing can help identify embryos with chromosomal abnormalities and prevent their implantation. additionally, pre-conception counseling can help identify any potential risk factors that may lead to these abnormalities.