Agenesis, aplasia and hypoplasia of gallbladder
ICD-10 Q44.0 is a billable code used to indicate a diagnosis of agenesis, aplasia and hypoplasia of gallbladder.
Agenesis, aplasia, and hypoplasia of the gallbladder are congenital malformations characterized by the absence (agenesis), underdevelopment (hypoplasia), or incomplete development (aplasia) of the gallbladder. These conditions can lead to various digestive issues, as the gallbladder plays a crucial role in bile storage and release, which is essential for fat digestion. In pediatric patients, these conditions may be associated with other congenital anomalies, particularly those affecting the biliary tract and the digestive system. Symptoms may include abdominal pain, jaundice, and digestive disturbances. Diagnosis is typically made through imaging studies such as ultrasound or MRI, which can reveal the absence or abnormal size of the gallbladder. Management may involve dietary modifications and monitoring for complications, as surgical intervention is rarely required unless associated with other significant anomalies.
Detailed clinical notes including symptoms, imaging results, and any associated congenital conditions.
Pediatric patients presenting with abdominal pain, jaundice, or failure to thrive may require evaluation for gallbladder anomalies.
Pediatric coders should be aware of the developmental implications of gallbladder malformations and their potential impact on growth and nutrition.
Genetic testing results, family history of congenital conditions, and any syndromic associations.
Genetic counseling for families with a history of congenital digestive anomalies, including gallbladder malformations.
Consideration of chromosomal abnormalities that may be associated with gallbladder agenesis or hypoplasia, such as trisomy 18.
Used in cases where gallbladder anomalies lead to complications requiring surgical intervention.
Surgical reports detailing the findings and procedures performed.
Pediatric surgeons should document any congenital findings during surgery.
Common symptoms include jaundice, abdominal pain, and failure to thrive. These symptoms arise due to the lack of bile storage and release, which is critical for digestion.
