Atrichia with papular lesions is a rare inherited form of alopecia characterized by irreversible hair loss during the neonatal period on all hear-bearing areas of the body, later associated with the d...
Comprehensive, easy-to-understand information about this condition
How we create this content →Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 31, 2026
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 31, 2026
The documentation for atrichia with papular lesions is limited primarily due to its rarity, which affects fewer than a few hundred individuals worldwide. This extreme rarity restricts the ability to conduct large-scale clinical studies, and the condition's clinical features are still being characterized as research progresses. The genetic basis was only recently identified, which adds to the ongoing efforts to understand the full clinical spectrum.
To navigate your care effectively, consider seeking a dermatologist with expertise in genetic skin disorders. Genetic counseling may be beneficial for understanding the implications of the HR gene variants for you and your family. Although no patient organizations are currently identified, resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide support and information. Participating in clinical trials may also offer access to cutting-edge research and potential therapies.
Currently, there are 21 active clinical trials related to atrichia with papular lesions. These trials may explore various aspects of the condition and potential treatments. You can find more information about these studies on ClinicalTrials.gov by searching for 'atrichia with papular lesions'. While there are no orphan drug designations at this time, the active research offers hope for future therapeutic options.
Actionable guidance for navigating care for atrichia with papular lesions
To navigate your care effectively, consider seeking a dermatologist with expertise in genetic skin disorders. Genetic counseling may be beneficial for understanding the implications of the HR gene variants for you and your family. Although no patient organizations are currently identified, resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide support and information. Participating in clinical trials may also offer access to cutting-edge research and potential therapies.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
Inheritance patterns describe how genetic conditions are passed from parents to children.
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 31, 2026
Consider asking your healthcare providers these condition-specific questions
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center
AI-Generated Content: This summary was generated using AI. Content has been fact-checked. Always consult with qualified healthcare providers for medical guidance.
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.