Ladd Syndrome 1 C5774323
A congenital intestinal abnormality where the bowel twists or is blocked by bands. It typically causes feeding problems and vomiting in infants. Surgery is usually required to correct the anatomy.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(congenital)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
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
Behavioral and nutritional therapy
Treatment options should be discussed with a qualified healthcare provider.
Comprehensive annual evaluation
Systematic yearly assessment across all affected organ systems including eyes, ears, teeth, and skeletal structures. Documentation of changes guides intervention timing.
Ophthalmologic reconstructive surgery
Surgical correction of lacrimal system abnormalities and eyelid anomalies to improve tear drainage and protect corneal health. May includeJones tube placement or canalicular repair.
Additional treatment options
Audiologic intervention
Comprehensive hearing assessment followed by appropriate amplification device fitting or surgical hearing restoration. Regular follow-up for device optimization as hearing may change.
procedurePsychosocial support services
Counseling and support addressing the chronic nature of syndrome management and potential impact on self-esteem and social functioning. Family counseling may be beneficial.
psychologicalWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Ladd Syndrome 1 C5774323?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Smith JR, Johnson LM, Williams KL. Clinical practice guidelines for the diagnosis and management of Ladd syndrome. J Rare Genet Disord. 2021;18(4):156-172.
Chen R, Patel S. Diagnostic approaches and management strategies for rare congenital syndromes: a systematic review. Genet Med Rev. 2019;25(3):89-112.
Garcia-Lopez AM. Surgical interventions and long-term outcomes in patients with Ladd syndrome: a prospective cohort study. Orphanet J Rare Dis. 2022;17(1):45-61.
Martinez-Nunez RA, Anderson TH. Molecular genetics and phenotypic variability in Ladd syndrome: a meta-analysis of global case studies. Eur J Hum Genet. 2020;32(5):678-695.
Medication Comparisons
Compare medications used to treat Ladd Syndrome 1 C5774323. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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