Q97 refers to Other sex chromosome abnormalities, female phenotype, not elsewhere classified, covering a range of chromosomal anomalies, such as trisomies, monosomies, deletions, and structural abnormalities, typically diagnosed prenatally or at birth.
Diagnosis is made through prenatal screenings (e.g., nuchal translucency scan, cell-free DNA tests), amniocentesis, karyotyping, and postnatal chromosomal analysis to identify specific chromosomal abnormalities.
ICD10 code Q97 is used extensively in prenatal care records, pediatric assessments, genetic counseling documentation, insurance claims, and research on chromosomal syndromes.
Q1: What is ICD10 code Q97?
A: It documents Other sex chromosome abnormalities, female phenotype, not elsewhere classified, referring to chromosomal abnormalities impacting physical, developmental, and cognitive outcomes.
Q2: Is Down syndrome genetic?
A: Yes, it is caused by an extra copy of chromosome 21.
Q3: What is the life expectancy for children with Trisomy 18?
A: Many affected infants have limited survival, although some live into adolescence with significant medical support.
Q4: Can chromosomal abnormalities be prevented?
A: No, but early diagnosis helps in planning appropriate care and interventions.
Q5: How is Turner's syndrome managed?
A: Management includes growth hormone therapy, estrogen replacement, and monitoring for associated health issues.
ICD10 code Q97 ensures comprehensive documentation of Other sex chromosome abnormalities, female phenotype, not elsewhere classified, aiding early detection, care planning, and improving outcomes for individuals with chromosomal disorders.
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