Butyrylcholinesterase Deficiency Fluoride Resistant Japanese Type C1867469
A genetic enzyme deficiency affecting how certain medications are broken down. The variant was first described in Japanese populations. Usually discovered incidentally during drug sensitivity testing.
Key facts at a glance
- ICD-10
- E88.9
- ICD-11
- 5A00.0
- Body system
- metabolic
- Severity
- mild
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Fatigue or weight changes
(metabolic)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Prolonged neuromuscular blockade after succinylcholine
(metabolic)Increased sensitivity to succinylcholine
(metabolic)Delayed recovery from anesthesia
(metabolic)Asymptomatic cholinesterase deficiency
(metabolic)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
Anesthesia protocol modification
Pre-operative identification allows use of alternative anesthetic agents and shortened neuromuscular blocking agents.
Healthy lifestyle changes and stress management
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Genetic confirmation testing
Definitive genetic testing to confirm BChE mutation status and guide clinical management decisions.
Additional treatment options
Medical alert identification
Wearing medical alert bracelet and carrying documentation of BChE deficiency for emergency medical situations.
lifestylePretreatment with butyrylcholinesterase
Fresh frozen plasma or purified BChE administration before elective surgery may restore normal drug metabolism.
medicationPatient and family education
Comprehensive education about condition implications, emergency precautions, and inheritance patterns.
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 Butyrylcholinesterase Deficiency Fluoride Resistant Japanese Type C1867469?
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.
Soliday FK, Conley YP, Henker R. Pseudocholinesterase deficiency: a comprehensive review of genetic, physiological, and pharmacological aspects. Anesthesiology. 2020;132(4):789-801.
American Society of Anesthesiologists. Practice guidelines for the management of patients with cholinesterase deficiency undergoing anesthesia. Anesthesiology Practice. 2022;18(2):45-62.
Yamamoto K, Tanaka H, Nakajima A, et al. Clinical outcomes of fluoride-resistant butyrylcholinesterase deficiency in Japanese patients: a prospective multicenter study. J Clin Anesth. 2021;68:110078.
Manecke GR, Butterworth JF. Butyrylcholinesterase deficiency and anesthetic complications. In: Miller's Anesthesia. 9th ed. Elsevier; 2023:892-915.
Medication Comparisons
Compare medications used to treat Butyrylcholinesterase Deficiency Fluoride Resistant Japanese Type C1867469. 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