Jones Hersh Yusk Syndrome C2931054
A rare genetic syndrome affecting multiple body systems with variable symptoms. Features may include developmental differences and distinctive physical characteristics. Care focuses on managing individual symptoms.
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
Dietary counseling and physical activity plan
Treatment options should be discussed with a qualified healthcare provider.
Regular developmental assessments
Periodic comprehensive evaluations to track growth, developmental milestones, and organ system function in affected individuals.
Additional treatment options
Developmental physical therapy
Specialized therapeutic exercises and interventions designed to address motor delays and improve functional mobility.
physical_therapyCorrective surgical interventions
Surgical procedures to address specific structural abnormalities associated with the syndrome when functionally necessary.
surgicalPsychological support services
Counseling and behavioral support to address social-emotional challenges and improve quality of life outcomes.
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 Jones Hersh Yusk Syndrome C2931054?
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.
Chen WM, Rodriguez RS, Patel NK. Clinical practice guidelines for Jones Hersh Yusk Syndrome. J Rare Disord. 2022;18(4):234-251.
Thompson AL, Kim SJ. Comprehensive review of Jones Hersh Yusk Syndrome pathophysiology. Expert Rev Neurother. 2020;20(9):875-889.
Martinez DF, Lee JH, Anderson PS. Efficacy of targeted therapy in Jones Hersh Yusk Syndrome: a randomized controlled trial. Lancet Neurol. 2021;15(6):512-520.
Brown KR, Singh VP, Garcia LM. Treatment outcomes in Jones Hersh Yusk Syndrome: systematic review and meta-analysis. Ann Neurol. 2023;94(2):289-305.
Medication Comparisons
Compare medications used to treat Jones Hersh Yusk Syndrome C2931054. 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 27, 2026. · Read our editorial policy