O35.14
Maternal care for (suspected) chromosomal abnormality in fetus, Turner Syndrome
Clinical Classification Guidelines
Medical Intelligence & Overview
Turner Syndrome is a condition that affects females, caused by a missing or incomplete X chromosome. When there is concern that a fetus might have this condition, specialized maternal care is provided to monitor the pregnancy and prepare for potential health needs after birth. ICD-10 code O35.14 is used to document cases where maternal care is focused on suspected chromosomal abnormalities, specifically Turner Syndrome, in the fetus.
Causes & Symptoms
Clinical Causes: Genetic anomaly involving the X chromosome, often missing or incomplete Random genetic mutations during conception No specific environmental or lifestyle factors are known to cause Turner Syndrome Familial history may occasionally be relevant, but most cases are sporadic
Key Symptoms: Most cases of Turner Syndrome are diagnosed prenatally through genetic testing Physical traits that may develop after birth, including short stature and swelling of hands and feet Delayed or incomplete development of secondary sexual characteristics during puberty Infertility issues due to ovarian failure Heart and kidney abnormalities detected through medical evaluations
Diagnostic & Treatment
Diagnosis Path: - Additional imaging tests to evaluate associated abnormalities in the heart or kidneys
Treatment Protocols: - Educational support and psychological counseling to address developmental challenges
Clinical Advice & FAQs
Billing Guidance
Is O35.14 a billable ICD-10 code?
Yes, O35.14 is a specific, billable code that can be used to indicate a diagnosis for reimbursement purposes.
Documentation
How do I report O35.14?
Clinical documentation must specify the nature of Maternal care for (suspected) chromosomal abnormality in fetus, Turner Syndrome and any associated comorbidities for accurate reporting.
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