Other specified congenital malformation syndromes affecting multiple systems
Chapter 17:Congenital malformations and chromosomal abnormalities
ICD-10 Q87 is a billable code used to indicate a diagnosis of other specified congenital malformation syndromes affecting multiple systems.
Congenital malformation syndromes affecting multiple systems can present a complex array of clinical features that may involve various organ systems, including the skin, breast, spleen, and adrenal glands. These syndromes often arise from genetic mutations or environmental factors during fetal development. Conditions such as ectodermal dysplasia, which affects skin and hair, or congenital adrenal hyperplasia, which impacts adrenal gland function, exemplify the diversity of manifestations. Patients may exhibit a combination of physical anomalies, functional impairments, and developmental delays. Accurate diagnosis often requires a multidisciplinary approach, including genetic testing, imaging studies, and clinical evaluations. The complexity of these syndromes necessitates thorough documentation to capture the full spectrum of associated anomalies and their implications for treatment and management.
Pediatric documentation must include growth parameters, developmental milestones, and specific physical findings related to congenital anomalies.
Common scenarios include newborns with multiple congenital anomalies requiring multidisciplinary care and follow-up.
Considerations include the need for ongoing developmental assessments and coordination of care among specialists.
Genetic documentation should include family history, results of genetic testing, and any syndromic diagnoses.
Scenarios often involve genetic counseling for families with a history of congenital anomalies or syndromes.
Genetic coding requires precise identification of syndromes and understanding of inheritance patterns.
Used in conjunction with Q87 for confirming genetic syndromes.
Documentation of clinical indications for testing and results.
Genetic specialists must ensure accurate coding based on test results.
Documentation must include a detailed description of the congenital anomalies, any genetic testing results, and the clinical implications of the condition. It is essential to specify the associated systems affected and any treatments or interventions planned.
