Jejunal Atresia With Renal Adysplasia C1865209
A rare condition combining intestinal blockage with underdeveloped or absent kidneys. Affects newborns and requires coordinated surgical and kidney function management.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- severe
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Intestinal obstruction
Malrotation with volvulus
Generalized symptoms
(congenital)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Feeding intolerance in newborn
(gastrointestinal)Renal agenesis
(genitourinary)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Combined jejunal atresia repair with renal assessment
Surgical correction of jejunal atresia with concurrent urological evaluation and intervention as needed. Requires coordination between pediatric surgery and urology teams to address both organ systems.
Drug therapy and clinical monitoring
Active treatment with regular monitoring by a healthcare provider is recommended.
Renal function surveillance
Regular monitoring of renal function through serum creatinine, electrolytes, and imaging studies to assess kidney development and function in patients with renal adysplasia component.
Additional treatment options
Central venous access for TPN
Placement of central venous catheter for long-term parenteral nutrition support, critical for neonates unable to tolerate enteral feeds until intestinal function recovers.
procedureManagement of associated complications
Pharmacological management of complications including gastroesophageal reflux, constipation, and electrolyte abnormalities commonly associated with both intestinal and urinary tract anomalies.
medicationDevelopmental follow-up program
Long-term multidisciplinary follow-up addressing growth, nutrition, renal health, and developmental milestones given the complex nature of this syndrome affecting multiple organ systems.
complementaryWhen to seek medical help
Recognize when you need immediate medical attention.
See a doctor within 24 hours
Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.
Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.
Frequently asked questions
Common questions about this topic.
What is Jejunal Atresia With Renal Adysplasia C1865209?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
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This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy