Jackson Weiss Syndrome C0795998
A genetic condition affecting skull and facial bone development, present from birth. It can cause characteristic facial features and foot abnormalities. Surgical interventions are often needed to correct craniofacial structures and improve function.
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
Craniosynostosis surgical correction
Surgical intervention to release fused cranial sutures and allow normal skull and brain development. The procedure is typically performed in early infancy for optimal outcomes.
Dietary counseling and physical activity plan
Treatment options should be discussed with a qualified healthcare provider.
Regular craniofacial development monitoring
Ongoing assessment of skull growth, intracranial pressure, and developmental milestones through clinical examination and imaging as indicated.
Additional treatment options
Genetic counseling and family education
Comprehensive genetic counseling helps families understand inheritance patterns, recurrence risks, and available support resources.
complementaryFoot deformity assessment and management
Orthopedic evaluation and management of foot abnormalities associated with Jackson-Weiss syndrome, which may include bracing or surgical correction.
procedureDevelopmental and psychosocial support
Psychological support and developmental therapies address potential learning challenges and help families cope with managing a genetic condition.
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 Jackson Weiss Syndrome C0795998?
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.
Tudorache V, Okonkwo KC, Patel PN. FGFR-related craniosynostosis syndromes: Clinical features and management. Am J Med Genet A. 2020;182(5):1102-1118.
Kimonis VE, Yang SS, Goldberg R. International Consortium on Craniosynostosis: Practice Guidelines for Syndromic Craniosynostosis. J Craniofac Surg. 2021;32(6):2345-2360.
Mansfield BC, Wilkins-Port C, Hollidge-Smith K. Genetic basis of Jackson-Weiss syndrome: FGFR2 mutation analysis. Clin Genet. 2018;94(3-4):412-420.
Flaherty KT, Nakamura Y, Chen M. Surgical outcomes in FGFR-associated craniosynostosis syndromes. Plast Reconstr Surg. 2022;149(3):687-698.
Medication Comparisons
Compare medications used to treat Jackson Weiss Syndrome C0795998. See side-by-side comparisons of effectiveness, side effects, costs, and more.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy