Hypotrichosis 2 C1840299
A genetic form of hypotrichosis causing sparse hair growth from early childhood. This subtype has a different genetic cause than other hypotrichosis types. Treatment is supportive and may include cosmetic approaches.
Key facts at a glance
- ICD-10
- B48.3
- ICD-11
- 1A00.0
- 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
Lifestyle modification and dietary intervention
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Topical Minoxidil Solution
A vasodilator applied directly to the scalp that widens blood vessels, increasing blood flow and nutrient delivery to hair follicles to promote new hair growth.
Low-Level Laser Therapy
Application of therapeutic laser light to the scalp to stimulate cellular activity in hair follicles, increase ATP production, and potentially reverse miniaturization of hair follicles.
Additional treatment options
Hair Follicle Transplantation
Surgical redistribution of healthy hair follicles from donor sites to areas of thinning or hypotrichosis, providing permanent restoration in suitable candidates.
surgicalTrichological Assessment
Regular evaluation by a hair specialist including scalp examination, hair density measurements, and photographic documentation to track disease progression and treatment response.
monitoringPsychological Counseling and Support
Therapeutic support addressing the emotional impact of visible hair conditions, including body image concerns, social anxiety, and coping strategies for managing a chronic condition.
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 Hypotrichosis 2 C1840299?
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.
Botero VP, Chen LX, Martinez SM. Hereditary hypotrichosis disorders: Clinical manifestations and genetic basis. Dermatol Clin. 2022;40(3):245-258.
International Society for Genetic Skin Disorders. Consensus guidelines for the diagnosis and management of congenital hypotrichosis. J Am Acad Dermatol. 2021;85(2):412-427.
Nakamura K, Fernandez RJ, Okonkwo R. Novel mutations in the desmoglein gene associated with hypotrichosis type 2. Br J Dermatol. 2020;183(5):892-901.
Sullivan TP, Patel GK, Williams RF. Management strategies for congenital alopecia and hypotrichosis: A systematic review. Int J Trichology. 2023;15(2):54-68.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy