Disease: Phacomatosis pigmentovascularis
- [Translated article] Bilateral Temporal Arachnoid Cysts Associated With Phakomatosis Cesioflammea
- <em>Cutis tricolor</em>: a literature review and report of five new cases
- <em>GNA11</em> brain somatic pathogenic variant in an individual with phacomatosis pigmentovascularis
- A Case of Phacomatosis Pigmentovascularis Type IIa in a Korean Infant
- A case of phakomatosis pigmentovascularis type II: port-wine stain and dermal melanocytosis with cutis marmorata telangiectatica congenita-like lesions
- A female infant with phacomatosis pigmentovascularis and congenital chylous ascites: A case report
- A Neonatal Case of Phacomatosis Pigmentovascularis Type IIa
- A rare case of phakomatosis pigmentovascularis type IIb associated with inverse Klippel-Trenaunay syndrome and Sturge-Weber syndrome
- An unusual case of phakomatosis pigmentovascularis type IIb with Becker's nevus
- Bilateral Phacomatosis Pigmentovascularis in a Young Male with Developmental Glaucoma and Varicose Veins
- Bilateral Temporal Arachnoid Cysts Associated With Phakomatosis Cesioflammea
- Blotchy baby: a case of phakomatosis pigmentovascularis
- Born in the Purple: An Exceptional Case of Cutis Marmorata Telangiectatica Congenita
- Choroidal melanoma in phacomatosis pigmentovascularis cesioflammea
- Choroidal melanoma in phacomatosis pigmentovascularis cesioflammea
- CHOROIDAL MELANOMA IN PHAKOMATOSIS PIGMENTOVASCULARIS WITH KLIPPEL-TRENAUNAY SYNDROME
- CHOROIDAL MELANOMA IN PHAKOMATOSIS PIGMENTOVASCULARIS WITH OVERLAPPING STURGE-WEBER SYNDROME AND KLIPPEL-TRENAUNAY SYNDROME
- Clinical characteristics and treatment of 52 cases of phakomatosis pigmentovascularis
- Complete agenesis of the corpus callosum in phacomatosis pigmentovascularis cesioflammea: a manifestation of mosaicism?
- Congenital telangiectatic und pigmented lesions associated with lymphedema, difference in leg length, and scoliosis
- Cutis marmorata telangiectatica congenita and aberrant Mongolian spots: Type V phacomatosis pigmentovascularis or phacomatosis cesiomarmorata
- Dermoscopic features of Phakomatosis pigmentovascularis type II: An underutilized tool!
- Early-Onset Glaucoma Manifesting as Buphthalmos in an Infant with Phakomatosis Pigmentovascularis Type IIa
- Extensive red and blue patches in a young girl
- Extensive subarachnoid venous angiomatosis with hydrocephalus in phacomatosis pigmentovascularis
- Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review
- Fluorescein angiography findings in phacomatosis pigmentovascularis
- Glaucoma in Phacomatosis Pigmentovascularis in a Young African Adolescent Boy: A Case Report
- GNA11 brain somatic pathogenic variant in an individual with phacomatosis pigmentovascularis
- Hematoporphyrin monomethyl ether-mediated photodynamic therapy for phakomatosis pigmentovascularis type Ⅱ: A case report
- Hematoporphyrin monomethyl ether-mediated photodynamic therapy temporarily relieves severe pruritis from phakomatosis pigmentovascularis: A case report
- Intramedullary and retroperitoneal melanocytic tumor associated with congenital blue nevus and nevus flammeus: an uncommon combination of neurocutaneous melanosis and phacomatosis pigmentovascularis--case report
- Introduction to phacomatoses (neurocutaneous disorders) in childhood
- Kikuchi-Fujimoto disease in patient with systemic phacomatosis pigmentovascularis
- Laser therapy treatment of phacomatosis pigmentovascularis type II: two case reports
- Mongolian spots combined with halo-like disappearance surrounding café au lait spots
- Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis
- Mosaic GNA11 mutations and a second hit in KRAS in phakomatosis pigmentovascularis are associated with intraosseous arteriovenous malformations in the jaw
- Mosaic Neurocutaneous Disorders and Their Causes
- Mosaic neurofibromatosis type 1, not phacomatosis pigmentovascularis
- Naevus vascularis mixtus and mixed vascular naevus syndrome
- New case of phacomatosis cesio-flammeo-marmorata: the time is right to review the classification for phacomatosis pigmentovascularis
- Ocular features in a patient presenting with a rare combination of multiple phakomatoses
- Ocular manifestations in phakomatosis pigmentovascularis: Current concepts on pathogenesis, diagnosis, and management
- Ocular manifestations of facial port-wine stain, nevus of Ota, and phakomatosis pigmentovascularis in Asian patients
- Ophthalmic Alterations in the Sturge-Weber Syndrome, Klippel-Trenaunay Syndrome, and the Phakomatosis Pigmentovascularis: An Independent Group of Conditions?
- Oral healthcare management of a child with phakomatosis pigmentovascularis associated with bilateral Sturge-Weber syndrome
- Outcomes of Infantile-Onset Glaucoma Associated With Port Wine Birthmarks and Other Periocular Cutaneous Vascular Malformation
- Outcomes of Management of Glaucoma in Phacomatosis Pigmentovascularis Over the Last Three Decades: A Single-Center Experience
- Outcomes of Microcatheter-Assisted Trabeculotomy for Glaucoma Associated With Sturge-Weber Syndrome and Phakomatosis Pigmentovascularis
- Pathophysiology and management of glaucoma associated with phakomatoses
- Patient with extensive Mongolian spots, nevus flammeus and nevus vascularis mixtus: A novel case of phacomatosis pigmentovascularis
- Phacomatosis cesioflammea in association with von Recklinghausen disease (neurofibromatosis type I)
- Phacomatosis Cesioflammea with Cutis Marmorata-like Lesions and Unusual Extracutaneous Abnormalities: Is It a Distinct disorder?
- Phacomatosis cesioflammea with Klippel Trenaunay syndrome: A rare association
- Phacomatosis cesiomarmorata with hypospadias and phacomatosis cesioflammea with Sturge-Weber syndrome, Klippel-Trenaunay syndrome and aplasia of veins -- case reports with rare associations
- Phacomatosis is Not a Twin-Spot Phenomenon
- Phacomatosis melanocesioflammea: the rediscovery of phacomatosis pigmentovascularis type IV
- Phacomatosis melanorosea without extracutaneous features: an unusual type of phacomatosis pigmentovascularis
- Phacomatosis Melanorosea: A Further Case of an Unusual Skin Disorder
- Phacomatosis pigmento-pigmentaria: should we add a new type of phacomatosis? Fact and controversies
- Phacomatosis pigmentovascularis
- Phacomatosis Pigmentovascularis is Not a Twin-Spot Phenomenon
- Phacomatosis pigmentovascularis of cesioflammea type
- Phacomatosis pigmentovascularis spilorosea and mutation in the PTPN11 gene: new case with significant neurologic impairment
- Phacomatosis pigmentovascularis spilorosea mit Mutation im PTPN11 Gen: neuer Fall mit erheblichen neurologischen Beeintrachtigungen
- Phacomatosis pigmentovascularis type 2b (phacomatosis cesioflammea) with double superior vena cava, abdominal varicosities, and natal tooth: Novel associations
- Phacomatosis pigmentovascularis type IIa--case report
- Phacomatosis pigmentovascularis type IIB associated with Sturge-Weber syndrome: a case report and review of the literature
- Phacomatosis Pigmentovascularis Type Vb in a Three-Year Old Boy
- Phacomatosis pigmentovascularis with Raynaud's phenomena
- Phacomatosis pigmentovascularis with sturge-weber syndrome and congenital glaucoma: A rare case report
- Phacomatosis pigmentovascularis: Report of four new cases
- Phacomatosis Pigmentovascularis: Simple Presentation of a Not So Simple Dermatological Condition
- Phacomatosis spilorosea versus phacomatosis melanorosea: a critical reappraisal of the worldwide literature with updated classification of phacomatosis pigmentovascularis
- Phakomatosis Pigmentovascularis
- Phakomatosis Pigmentovascularis Associated With Sturge-Weber Syndrome, Ota Nevus, and Congenital Glaucoma
- Phakomatosis pigmentovascularis cesioflammea: a case report
- Phakomatosis pigmentovascularis Ib with left-sided hemihypertrophy, interdigital gaps and scoliosis: a unique case of phakomatosis pigmentovascularis
- Phakomatosis pigmentovascularis IIb (phakomatosis cesioflammea) associated with the absence of infrarenal inferior vena cava
- Phakomatosis pigmentovascularis type IIb
- Phakomatosis pigmentovascularis type IIb in association with external hydrocephalus
- Phakomatosis pigmentovascularis type IIb with Klippel-Trenaunay syndrome: Association with GNAQ mutation in vascular endothelial cells
- Phakomatosis pigmentovascularis Type IIb, Sturge-Weber syndrome and cone shaped tongue: An unusual association
- Phakomatosis pigmentovascularis type IIb: A case with Klippel-Trenáunay syndrome and extensive dermal melanocytosis as nevus of Ota, nevus of Ito and ectopic Mongolian spots
- Phakomatosis pigmentovascularis type Ⅲa mainly manifested by zosteriform nevus spilus: A case report with dermoscopic features
- Port-wine stain as a clue for two rare coexisting entities
- PTPN11 Mosaicism Causes a Spectrum of Pigmentary and Vascular Neurocutaneous Disorders and Predisposes to Melanoma
- Raynaud's Phenomenon and Limb Hypertrophy Presenting Phacomatosis Pigmentovascularis: A Rare Association
- Red-white and blue baby: a case of phacomatosis pigmentovascularis type V
- Retinal Vascular Abnormalities in Phakomatosis Pigmentovascularis
- Segmental hypomelanosis and hypermelanosis arranged in a checkerboard pattern are distinct naevi: flag-like hypomelanotic naevus and flag-like hypermelanotic naevus
- Sturge-Weber Syndrome Associated with Monolateral Ocular Melanocytosis, Iris Mammillations, and Diffuse Choroidal Haemangioma
- Sturge-Weber syndrome in association with Klippel-Trenaunay syndrome and phakomatosis pigmentovascularis type IIb
- Syndromes with vascular skin anomalies
- The case of a boy with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita: a unique instance of phacomatosis pigmentovascularis
- The risk of glaucoma associated with phacomatosis cesioflammea and phacomatosis cesioflammeo-marmorata
- Unusual case of phakomatosis pigmentovascularis in a Japanese female infant associated with three phakomatoses: Port-wine stain, dermal melanocytosis and cutis marmorata telangiectatica congenita
- Vascular and Pigmented Lesions of Phacomatosis Pigmentovascularis Treated With a Combination of Long-Pulsed, Q-Switched Laser, and Picosecond Lasers
- Vascular malformation and common keratinocytic nevus of the soft type: phacomatosis pigmentovascularis revisited