phakomatosis pigmentovascularis
Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available
Phakomatosis Pigmentovascularis: A Complete Overview
Phakomatosis pigmentovascularis (PPV) is a rare congenital syndrome, predominantly consisting of a vascular malformation and dermal melanosis. PPV is a mosaic abnormality of vasomotor
Phakomatosis pigmentovascularis
Phakomatosis pigmentovascularis is a rare neurocutanous condition where there is coexistence of a capillary malformation (port-wine stain) with various melanocytic lesions, including dermal
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Phakomatosis pigmentovascularis | About the Disease | GARD
Phakomatosis pigmentovascularis is caused by genetic mutations, also known as pathogenic variants. Genetic mutations can be hereditary, when parents pass them down to their children,
Ocular manifestations in phakomatosis pigmentovascularis: Current
Phakomatosis pigmentovascularis is a rare congenital multisystemic disease with variable manifestations where a vascular malformation of the skin is associated with a
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Phakomatosis Pigmentovascularis: A Clinical Profile of 11 Indian
Phakomatosis pigmentovascularis (PPV) is a rare congenital syndrome characterized by the simultaneous presence of capillary malformation and pigmentary nevi. The objective of our