Any skin basal cell carcinoma in which the cause of the disease is a mutation in the TP53 gene.
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 7, 2026
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 7, 2026
The documentation surrounding basal cell carcinoma, susceptibility to, 7 is limited primarily due to its rarity and the recent recognition of its genetic basis. Conditions like BCC7, which affect fewer individuals, often do not undergo extensive clinical studies, leading to gaps in understanding the full spectrum of clinical features and management strategies. This situation can be frustrating, but ongoing research may provide more insights in the future.
To navigate your condition effectively, consider consulting a dermatologist with expertise in hereditary skin cancers. They can provide insights into monitoring and managing your risk for basal cell carcinoma. Additionally, genetic counseling may be beneficial, especially for family planning and understanding the implications of the autosomal dominant inheritance pattern. Although there are currently no specific patient organizations for BCC7, resources such as the National Organization for Rare Disorders (NORD) at rarediseases.org may offer valuable information and support. Engaging with a genetic counselor can also help you explore testing options and family implications.
Actionable guidance for navigating care for basal cell carcinoma, susceptibility to, 7
To navigate your condition effectively, consider consulting a dermatologist with expertise in hereditary skin cancers. They can provide insights into monitoring and managing your risk for basal cell carcinoma. Additionally, genetic counseling may be beneficial, especially for family planning and understanding the implications of the autosomal dominant inheritance pattern. Although there are currently no specific patient organizations for BCC7, resources such as the National Organization for Rare Disorders (NORD) at rarediseases.org may offer valuable information and support. Engaging with a genetic counselor can also help you explore testing options and family implications.
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 7, 2026
Consider asking your healthcare providers these condition-specific questions
Online Mendelian Inheritance in Man
AI-Generated Content: This summary was generated using AI. 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.