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Noonan Syndrome 2 C1854469

Published: July 22, 2026Updated: August 20, 2026

A genetic condition affecting multiple body systems, characterized by distinctive facial features, heart defects, and skeletal abnormalities. Similar to other Noonan syndromes, it requires multidisciplinary care.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

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

1

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

1

Dietary counseling and physical activity plan

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
2

Multisystem Surveillance Protocol

Systematic monitoring of cardiac, developmental, and growth parameters due to the variable expressivity associated with KRAS-related Noonan syndrome. Regular specialist consultations ensure comprehensive care.

monitoring
3

Cardiac Medication Management

Pharmacological treatment for hypertrophic cardiomyopathy or arrhythmias including beta-blockers and calcium channel blockers as appropriate. Medication choice depends on specific cardiac pathology and symptom severity.

medication

Additional treatment options

Orthopedic Intervention

Surgical correction of chest wall deformities such as pectus excavatum or carinatum when causing functional impairment or significant cosmetic concern. Procedures may include the Nuss or Ravitch technique.

surgical

Nutritional Support Program

Calorie-dense nutritional supplementation and feeding support for patients with feeding difficulties or failure to thrive. Registered dietitian involvement ensures adequate macro and micronutrient intake.

dietary

Lymphedema Management

Comprehensive decongestive therapy including manual lymphatic drainage, compression garments, and skin care for lymphatic abnormalities. Ongoing maintenance therapy prevents complications.

complementary

When to seek medical help

Recognize when you need immediate medical attention.

Schedule an appointment soon

Symptoms associated with this condition. Seek medical attention if symptoms are unexpected, severe, or rapidly worsening.- Contact your healthcare provider if symptoms persist or worsen. Seek emergency care for sudden severe symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Noonan Syndrome 2 C1854469?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Roberts AE, Allanson JE, Tartaglia M, Gelb BD. Noonan syndrome. Lancet. 2013;381(9863):333-342.

guideline2013
2

Tartaglia M, Gelb BD, Zenker M. Noonan syndrome and clinically related disorders. Best Pract Res Clin Endocrinol Metab. 2011;25(1):161-179.

review2011
3

Kratz CP, Zhanel M, Zugmaier G, et al. Comparison of the RASopathies: Clinical and molecular aspects in 58 patients. Am J Med Genet A. 2020;182(5):1076-1086.

clinical_trial2020
4

Croonen EA, Harmsen M, Van der Burgt I, et al. Noonan syndrome: The RAS-MAPK pathway disorders. Eur J Med Genet. 2019;62(8):103647.

review2019

Medication Comparisons

Compare medications used to treat Noonan Syndrome 2 C1854469. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy