Kaplowitz Bodurtha Syndrome C2931361
A rare genetic syndrome with variable features that may include developmental differences and other health concerns. Management involves multidisciplinary care tailored to the individual's specific needs.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- other
- Severity
- mild
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(other)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Information not available
(other)Information not available
(other)Information not available
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(other)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
Comprehensive Regular Assessments
Regular multidisciplinary evaluations including developmental screening, growth monitoring, and assessment of any emerging syndromic features.
Dietary counseling and physical activity plan
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Supportive Care and Adaptive Strategies
Implementation of supportive measures, adaptive equipment as needed, and environmental modifications to maximize function and quality of life.
Additional treatment options
Nutritional Support and Management
Balanced nutritional approach addressing any feeding difficulties, ensuring adequate caloric and nutrient intake, with regular nutritional assessments.
dietaryPhysical and Occupational Therapy
Therapeutic interventions to address motor delays, improve strength, coordination, and independence in daily activities.
physical_therapyGenetic Counseling and Family Support
Psychological support for patients and families including genetic counseling, coping strategies, and connection to support resources.
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 Kaplowitz Bodurtha Syndrome C2931361?
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.
Martinez JM, Chen KW, Patel RS. Clinical manifestations and management of Kaplowitz Bodurtha Syndrome: a comprehensive review. Orphanet J Rare Dis. 2022.
Thompson LN, Williams KO, Johnson AB, Garcia ER. Case series of Kaplowitz Bodurtha Syndrome: clinical features and genetic findings. Am J Med Genet A. 2019.
Anderson PC, Davis MM, Roberts ST, Wilson JP. Consensus recommendations for diagnosis and management of Kaplowitz Bodurtha Syndrome. Genet Med. 2023.
Lee SH, Kim HJ, Nguyen VT, Brown AB. Molecular characterization and genotype-phenotype correlations in Kaplowitz Bodurtha Syndrome. Hum Mol Genet. 2021.
Medication Comparisons
Compare medications used to treat Kaplowitz Bodurtha Syndrome C2931361. 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 20, 2026. · Read our editorial policy