Cleft uvula
ICD-10 Q35.7 is a billable code used to indicate a diagnosis of cleft uvula.
Cleft uvula is a congenital malformation characterized by a split or cleft in the uvula, the small, fleshy extension at the back of the throat. This condition can occur in isolation or as part of a more complex syndrome, such as cleft palate or other craniofacial anomalies. The cleft may vary in size and can lead to difficulties in feeding, speech, and increased risk of ear infections due to improper closure of the nasopharynx. In some cases, it may be associated with other congenital malformations of the respiratory system, such as choanal atresia, where the nasal passage is blocked, or tracheoesophageal fistula, where there is an abnormal connection between the trachea and esophagus. Lung hypoplasia, a condition where the lungs are underdeveloped, can also be a concern in infants with significant congenital anomalies. Early diagnosis and intervention are crucial for managing these conditions, often requiring a multidisciplinary approach involving pediatricians, otolaryngologists, and speech therapists.
Detailed clinical notes on the infant's feeding difficulties, speech development, and any associated respiratory issues.
Infants presenting with cleft uvula during routine examinations, referrals for speech therapy, or surgical interventions.
Consideration of the infant's overall health and any additional congenital anomalies that may impact treatment.
Genetic testing results, family history of congenital conditions, and any syndromic associations.
Genetic counseling sessions for families with a history of cleft conditions or syndromes associated with cleft uvula.
Understanding the genetic implications and potential for recurrence in future pregnancies.
Performed in cases of cleft uvula to restore normal anatomy.
Operative report detailing the procedure and any complications.
Pediatric otolaryngology may have specific protocols for uvula repair.
Accurate coding of cleft uvula is crucial for appropriate reimbursement, tracking of congenital conditions, and ensuring that patients receive the necessary multidisciplinary care. It also aids in research and understanding the prevalence and outcomes of congenital anomalies.
