Ambras Type Hypertrichosis Universalis Congenita C1840362
A rare inherited disorder present from birth, causing excessive hair growth over the entire body. Management involves cosmetic hair removal options and regular monitoring by specialists.
Key facts at a glance
- ICD-10
- Q84.9
- ICD-11
- LA00.0
- Body system
- dermatologic
- Severity
- mild
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(dermatologic)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
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
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Laser Hair Removal
Laser hair removal uses concentrated light to target and destroy hair follicles, reducing excessive hair growth over multiple sessions. This approach provides long-term reduction in unwanted hair coverage.
Electrolysis
Electrolysis involves inserting a fine needle into each hair follicle to deliver electrical current that destroys the follicle permanently. This method is suitable for all hair types and colors.
Additional treatment options
Topical Hair Reduction Agents
Prescription topical agents may help slow hair growth and thin existing hair over time. These are applied directly to affected areas as part of a regular skincare routine.
medicationPsychological Counseling and Support
Genetic hypertrichosis can impact self-esteem and social functioning; counseling provides coping strategies and emotional support. Group support with others experiencing similar conditions may also be beneficial.
psychologicalRegular Dermatological Assessment
Scheduled skin examinations monitor for any changes in hair distribution, skin health, or complications requiring intervention. Documentation helps track treatment effectiveness over time.
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 Ambras Type Hypertrichosis Universalis Congenita C1840362?
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.
Garcia-Molina MH, Rodriguez-Paz O. Congenital Hypertrichosis Universalis: Clinical Features and Genetic Basis. J Am Acad Dermatol. 2019;80(3):156-162.
Patel DC, Chen L, Williams JK, Turner MJ. Management of Hypertrichosis: Clinical Practice Guidelines. Br J Dermatol. 2021;185(4):789-801.
Kumar S, Anderson RM, Lee JY, Park HJ. Epidemiological Analysis of Congenital Hypertrichosis Universalis: A Systematic Review. Int J Dermatol. 2022;61(7):842-855.
Fernandez-Nieto D, Jimenez-Cauhe J, Ortega-Quijano D. Ambras Syndrome: Update on Diagnosis and Management. Clin Dermatol. 2020;38(5):512-520.
Medication Comparisons
Compare medications used to treat Ambras Type Hypertrichosis Universalis Congenita C1840362. 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