Loss of scalp and body hair involving microscopically inflammatory patchy areas.
Comprehensive, easy-to-understand information about this condition
How we create this content →The documentation surrounding alopecia areata is limited primarily due to its variable presentation and the fact that it affects a relatively small population. This has resulted in fewer systematic clinical studies. Additionally, the lack of identified genetic factors complicates the understanding of its pathophysiology and inheritance, leaving many patients and families seeking clarity.
To navigate alopecia areata, consider consulting a dermatologist specializing in hair disorders for tailored management strategies. Additionally, the National Alopecia Areata Foundation provides valuable resources and support for individuals affected by this condition. You can explore their website at https://naaf.org for information on support groups and educational materials. Participating in clinical trials may also provide access to cutting-edge treatments and contribute to ongoing research efforts.
Currently, there are 161 active clinical trials investigating various aspects of alopecia areata. While there are no orphan drug designations, the research landscape is promising, with multiple studies exploring potential treatments and management strategies. You can find more details about these trials by visiting ClinicalTrials.gov and searching for 'alopecia areata'.
Actionable guidance for navigating care for alopecia areata
To navigate alopecia areata, consider consulting a dermatologist specializing in hair disorders for tailored management strategies. Additionally, the National Alopecia Areata Foundation provides valuable resources and support for individuals affected by this condition. You can explore their website at https://naaf.org for information on support groups and educational materials. Participating in clinical trials may also provide access to cutting-edge treatments and contribute to ongoing research efforts.
Consider asking your healthcare providers these condition-specific questions
Connect with organizations supporting the alopecia areata community
Helpful links for rare disease information and support
The documentation surrounding alopecia areata is limited primarily due to its variable presentation and the fact that it affects a relatively small population. This has resulted in fewer systematic clinical studies. Additionally, the lack of identified genetic factors complicates the understanding of its pathophysiology and inheritance, leaving many patients and families seeking clarity.
To navigate alopecia areata, consider consulting a dermatologist specializing in hair disorders for tailored management strategies. Additionally, the National Alopecia Areata Foundation provides valuable resources and support for individuals affected by this condition. You can explore their website at https://naaf.org for information on support groups and educational materials. Participating in clinical trials may also provide access to cutting-edge treatments and contribute to ongoing research efforts.
Currently, there are 161 active clinical trials investigating various aspects of alopecia areata. While there are no orphan drug designations, the research landscape is promising, with multiple studies exploring potential treatments and management strategies. You can find more details about these trials by visiting ClinicalTrials.gov and searching for 'alopecia areata'.
Actionable guidance for navigating care for alopecia areata
To navigate alopecia areata, consider consulting a dermatologist specializing in hair disorders for tailored management strategies. Additionally, the National Alopecia Areata Foundation provides valuable resources and support for individuals affected by this condition. You can explore their website at https://naaf.org for information on support groups and educational materials. Participating in clinical trials may also provide access to cutting-edge treatments and contribute to ongoing research efforts.
Consider asking your healthcare providers these condition-specific questions
Connect with organizations supporting the alopecia areata community
Helpful links for rare disease information and support
The documentation surrounding alopecia areata is limited primarily due to its variable presentation and the fact that it affects a relatively small population. This has resulted in fewer systematic clinical studies. Additionally, the lack of identified genetic factors complicates the understanding of its pathophysiology and inheritance, leaving many patients and families seeking clarity.
To navigate alopecia areata, consider consulting a dermatologist specializing in hair disorders for tailored management strategies. Additionally, the National Alopecia Areata Foundation provides valuable resources and support for individuals affected by this condition. You can explore their website at https://naaf.org for information on support groups and educational materials. Participating in clinical trials may also provide access to cutting-edge treatments and contribute to ongoing research efforts.
Currently, there are 161 active clinical trials investigating various aspects of alopecia areata. While there are no orphan drug designations, the research landscape is promising, with multiple studies exploring potential treatments and management strategies. You can find more details about these trials by visiting ClinicalTrials.gov and searching for 'alopecia areata'.
Actionable guidance for navigating care for alopecia areata
To navigate alopecia areata, consider consulting a dermatologist specializing in hair disorders for tailored management strategies. Additionally, the National Alopecia Areata Foundation provides valuable resources and support for individuals affected by this condition. You can explore their website at https://naaf.org for information on support groups and educational materials. Participating in clinical trials may also provide access to cutting-edge treatments and contribute to ongoing research efforts.
Consider asking your healthcare providers these condition-specific questions
Connect with organizations supporting the alopecia areata community
Helpful links for rare disease information and support
Clinical profile data for this condition is not yet available. Phenotype information may still be loading below.
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Feb 8, 2026
Patient Advocacy Groups (PAGs) provide support, resources, and community for patients and caregivers.
Consider asking your healthcare providers these condition-specific questions
Genetic and Rare Diseases Info Center
1 peer-reviewed source from PubMed
AI-Generated Content: This summary was generated using AI. Content has been fact-checked. Always consult with qualified healthcare providers for medical guidance.
Organizations with approved therapies for this disease
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.