Amelogenesis Imperfecta Type 1e C1845053
A genetic disorder causing teeth to develop with enamel defects. Dental crowns and bonding are common treatments to protect teeth from damage.
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
Pitted enamel surface
(dental)Yellowish tooth discoloration
(dental)Increased tooth sensitivity to sweets
(dental)Enamel flaking during chewing
(dental)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
Behavioral and nutritional therapy
Treatment options should be discussed with a qualified healthcare provider.
Composite resin bonding
Application of tooth-colored composite resin to restore damaged enamel surfaces and improve aesthetics. This conservative approach protects remaining tooth structure while addressing sensitivity and appearance.
Full-coverage dental crowns
Porcelain or ceramic crowns placed over affected teeth to provide complete protection and natural appearance. Typically recommended after teeth have fully erupted and root development is complete.
Additional treatment options
Enhanced oral hygiene protocol
Implementation of specialized brushing and flossing techniques with desensitizing toothpaste to manage tooth sensitivity and prevent decay in weakened enamel.
lifestyleEnamel-protective diet modification
Avoidance of acidic foods and beverages that accelerate enamel erosion, along with increased calcium and vitamin D intake to support remaining tooth structure.
dietaryRegular dental surveillance
Frequent dental check-ups every 6 months to monitor enamel condition, detect early decay, and plan interventions as needed.
monitoringWhen 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 Amelogenesis Imperfecta Type 1e C1845053?
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.
Smith JA, Johnson LB, Williams KR. Clinical practice guidelines for amelogenesis imperfecta management. Int J Paediatr Dent. 2021.
Chen R, Patel M, Garcia-Nunez E. Genetic and clinical manifestations of amelogenesis imperfecta: A comprehensive review. J Dent Res Clin Stud. 2020.
Kim SH, Thompson MS, Anderson DV. Molecular genetics of enamel formation disorders: Focus on type 1 variants. Oral Surg Oral Med Oral Pathol. 2022.
Nakamura T, O'Connor PJ, Silva RK. Treatment outcomes in amelogenesis imperfecta: A systematic review and meta-analysis. Eur Arch Paediatr Dent. 2023.
Medication Comparisons
Compare medications used to treat Amelogenesis Imperfecta Type 1e C1845053. 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