Angioma serpiginosum (AS) is a benign congenital skin disease characterized by progressive dilation of the subepidermal skin vessels manifesting as purple punctate lesions usually appearing on the low...
Comprehensive, easy-to-understand information about this condition
How we create this content →The documentation on angioma serpiginosum is limited primarily due to its extreme rarity, affecting fewer than 1 in 1,000,000 people worldwide. This low prevalence results in a lack of systematic clinical studies and comprehensive research. Additionally, the absence of identified genetic factors and established inheritance patterns further complicates the understanding of this condition, leaving many aspects of its etiology and management underexplored.
The clinical features of angioma serpiginosum include erythema, which is present in 80-99% of cases, and vascular skin abnormalities that also fall within the same frequency range. Patients may exhibit macules, which are flat, discolored spots on the skin, again observed in 80-99% of affected individuals. A less common feature is retinal vascular malformation, which occurs in 5-29% of cases. These features typically appear on the lower limbs and buttocks and can follow specific patterns on the skin.
To navigate your journey with angioma serpiginosum, consider consulting a dermatologist who specializes in vascular skin disorders. They can provide insights into managing your condition and any potential treatments. While there are currently no patient organizations specifically for AS, you can find general support through resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov. Although there are no registries or clinical trials available at this time, staying connected with healthcare providers can help you access information on any future developments.
Actionable guidance for navigating care for angioma serpiginosum
To navigate your journey with angioma serpiginosum, consider consulting a dermatologist who specializes in vascular skin disorders. They can provide insights into managing your condition and any potential treatments. While there are currently no patient organizations specifically for AS, you can find general support through resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov. Although there are no registries or clinical trials available at this time, staying connected with healthcare providers can help you access information on any future developments.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
The documentation on angioma serpiginosum is limited primarily due to its extreme rarity, affecting fewer than 1 in 1,000,000 people worldwide. This low prevalence results in a lack of systematic clinical studies and comprehensive research. Additionally, the absence of identified genetic factors and established inheritance patterns further complicates the understanding of this condition, leaving many aspects of its etiology and management underexplored.
The clinical features of angioma serpiginosum include erythema, which is present in 80-99% of cases, and vascular skin abnormalities that also fall within the same frequency range. Patients may exhibit macules, which are flat, discolored spots on the skin, again observed in 80-99% of affected individuals. A less common feature is retinal vascular malformation, which occurs in 5-29% of cases. These features typically appear on the lower limbs and buttocks and can follow specific patterns on the skin.
To navigate your journey with angioma serpiginosum, consider consulting a dermatologist who specializes in vascular skin disorders. They can provide insights into managing your condition and any potential treatments. While there are currently no patient organizations specifically for AS, you can find general support through resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov. Although there are no registries or clinical trials available at this time, staying connected with healthcare providers can help you access information on any future developments.
Actionable guidance for navigating care for angioma serpiginosum
To navigate your journey with angioma serpiginosum, consider consulting a dermatologist who specializes in vascular skin disorders. They can provide insights into managing your condition and any potential treatments. While there are currently no patient organizations specifically for AS, you can find general support through resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov. Although there are no registries or clinical trials available at this time, staying connected with healthcare providers can help you access information on any future developments.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
The documentation on angioma serpiginosum is limited primarily due to its extreme rarity, affecting fewer than 1 in 1,000,000 people worldwide. This low prevalence results in a lack of systematic clinical studies and comprehensive research. Additionally, the absence of identified genetic factors and established inheritance patterns further complicates the understanding of this condition, leaving many aspects of its etiology and management underexplored.
The clinical features of angioma serpiginosum include erythema, which is present in 80-99% of cases, and vascular skin abnormalities that also fall within the same frequency range. Patients may exhibit macules, which are flat, discolored spots on the skin, again observed in 80-99% of affected individuals. A less common feature is retinal vascular malformation, which occurs in 5-29% of cases. These features typically appear on the lower limbs and buttocks and can follow specific patterns on the skin.
To navigate your journey with angioma serpiginosum, consider consulting a dermatologist who specializes in vascular skin disorders. They can provide insights into managing your condition and any potential treatments. While there are currently no patient organizations specifically for AS, you can find general support through resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov. Although there are no registries or clinical trials available at this time, staying connected with healthcare providers can help you access information on any future developments.
Actionable guidance for navigating care for angioma serpiginosum
To navigate your journey with angioma serpiginosum, consider consulting a dermatologist who specializes in vascular skin disorders. They can provide insights into managing your condition and any potential treatments. While there are currently no patient organizations specifically for AS, you can find general support through resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov. Although there are no registries or clinical trials available at this time, staying connected with healthcare providers can help you access information on any future developments.
Consider asking your healthcare providers these condition-specific questions
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.
Consider asking your healthcare providers these condition-specific questions
European rare disease database
Genetic and Rare Diseases Info Center
AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.
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