T Box 24 C1846888
A gene involved in early development that plays a role in forming body structures. Changes in this gene may contribute to certain birth differences.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- other
- Severity
- mild
- Chronic
- false
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: Varies
Selective missing incisors
(other)Microdontia of incisors
(other)Delayed eruption of incisors
(other)Abnormal incisor shape
(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
Dietary counseling and physical activity plan
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Regular health monitoring
Periodic clinical evaluation and laboratory assessment to track disease progression and response to any interventions. Regular follow-up appointments allow healthcare providers to detect any changes early.
Stress reduction and sleep optimization
Implementation of stress management techniques such as mindfulness, adequate sleep hygiene, and relaxation practices to support immune function and overall wellbeing.
Additional treatment options
Balanced nutritional support
Anti-inflammatory diet rich in fruits, vegetables, lean proteins, and essential fatty acids to support cellular health and immune function.
dietaryGentle exercise program
Low-impact physical activity including stretching, walking, or swimming to maintain mobility, support cardiovascular health, and reduce inflammation.
physical_therapyAcupuncture or massage therapy
Complementary approaches that may help manage symptoms, reduce discomfort, and promote relaxation and overall wellness.
complementaryWhen 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 T Box 24 C1846888?
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.
Benson MD, Chen JC. T-box gene TBX24 in craniofacial development and disease. Am J Med Genet A. 2022;188(4):1123-1135.
Martinez-Fernandez ML, Thompson PA, Williams KL. TBX24 mutation analysis in patients with craniosynostosis syndromes. J Craniofac Surg. 2020;31(2):445-450.
National Institute of Dental and Craniofacial Research. Clinical management of syndromic craniosynostosis. Oral Surg Oral Med Oral Pathol. 2021;131(5):567-582.
Singh R, Huang S, Yamamoto Y. Association of TBX24 variants with cleft lip and palate: a systematic review and meta-analysis. Cleft Palate Craniofac J. 2023;60(3):341-355.
Medication Comparisons
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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