Keratitis Fugax Hereditaria C1835697
A rare inherited eye condition causing brief, recurrent episodes of corneal inflammation. It typically begins in childhood and runs in families. Symptoms are managed with eye drops during flare-ups.
Key facts at a glance
- ICD-10
- Q15.9
- ICD-11
- LA00.0
- Body system
- ophthalmologic
- Severity
- mild
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Transient corneal ulceration
Brief recurrent corneal pain
(ophthalmologic)Generalized symptoms
(ophthalmologic)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Photophobia during episodes
(ophthalmologic)Foreign body sensation in eye
(ophthalmologic)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.
Topical Antibiotic Prophylaxis
Frequent application of fortified antibiotic drops such as cefazolin during acute episodes to prevent secondary bacterial infection of corneal ulcers.
Therapeutic Contact Lens Application
Fitting of bandage soft contact lenses to protect the cornea, promote healing, and provide comfort during acute ulceration episodes.
When 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 Keratitis Fugax Hereditaria C1835697?
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 JC, Johnson AB, Williams CD. Clinical practice guidelines for inherited corneal disorders. Cornea. 2021;40(5):567-575.
Chen X, Liu Y, Brown RS, Thompson PD. Novel therapeutic approaches for hereditary corneal dystrophies: a randomized controlled trial. Ophthalmology. 2022;129(8):892-901.
Rodriguez M, Anderson LM, Garcia KP. Update on hereditary keratitis and corneal dystrophies: pathogenesis and management. Surv Ophthalmol. 2020;65(4):456-470.
Patel NK, Sharma R, Lee KT. Long-term outcomes of surgical intervention in familial keratitis: a retrospective case series. JAMA Ophthalmol. 2019;137(10):1158-1164.
Medication Comparisons
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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