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Journal of Investigative Dermatology, ISSN 0022-202X, 04/2016, Volume 136, Issue 4, pp. 770 - 778
Journal Article
ARCHIVOS ARGENTINOS DE PEDIATRIA, ISSN 0325-0075, 02/2018, Volume 116, Issue 1, pp. E121 - E124
Phakomatosis pigmentovascularis (PPV) is a syndrome characterized by the association of a vascular nevus with a congenital pigmented lesion... 
CLINICAL FINDINGS | phakomatosis cesioflammea | PEDIATRICS | phakomatosis pigmentovascularis | capillary vascular malformation | Mongolian spot | child | MOSAICISM
Journal Article
Indian Journal of Dermatology, ISSN 0019-5154, 5/2019, Volume 64, Issue 3, pp. 217 - 223
Introduction: Phakomatosis pigmentovascularis (PPV) is a rare congenital syndrome characterized by the simultaneous presence of capillary malformation and pigmentary nevi... 
Genetic disorders | Pay-per-view television | Glaucoma | Convulsions & seizures | Medical imaging | Congenital diseases | Lasers | Classification | Patients | Veins & arteries | nevus of Ota | Capillary malformation | seizure | Klippel-Trenaunay syndrome | phakomatosis pigmentovascularis | Short Communication
Journal Article
Indian Journal of Dermatology, ISSN 0019-5154, 01/2015, Volume 60, Issue 1, pp. 77 - 79
Phakomatosis pigmentovascularis (PPV) is a rare cutaneous disorder characterized by combination of capillary malformation and other pigmented naevi... 
phakomatosis | Sturge-Weber syndrome | Klippel-Trenaunay syndrome | DERMATOLOGY | Case studies | Rare diseases | Angiomatosis | Case Report
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 05/2020
.... To investigate the prevalence of glaucoma in patients with facial port-wine stains (PWS), nevus of Ota, and phakomatosis pigmentovascularis (PPV... 
Journal Article
Journal of Pediatric Neurosciences, ISSN 1817-1745, 07/2010, Volume 5, Issue 2, pp. 138 - 140
.... Phakomatosis pigmentovascularis represents the association of widespread, aberrant, and persistent nevus flammeus and pigmentary abnormalities... 
phakomatosis | Sturge-Weber syndrome | Klippel-Trenaunay syndrome | Care and treatment | Angiomatosis | Prognosis | Diagnosis | Comorbidity | Analysis | Nervous system | Klippel–Trenaunay syndrome | Sturge–Weber syndrome | Case Report
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 04/2008, Volume 146A, Issue 7, pp. 945 - 951
In 1947 the term phakomatosis pigmentovascularis (PPV) was coined to represent the association of widespread, aberrant, and persistent nevus flammeus and pigmentary abnormalities... 
nevus flammeus | nevi | phakomatosis | melanosis | Mongolian spots | NEVUS | GENETICS & HEREDITY
Journal Article
Archivos Argentinos de Pediatria, ISSN 0325-0075, 02/2018, Volume 116, Issue 1, pp. e121 - e124
Journal Article
Journal Article
The Journal of Dermatology, ISSN 0385-2407, 05/2004, Volume 31, Issue 5, pp. 415 - 418
.... She was otherwise well. She was diagnosed with phakomatosis pigmentovascularis (PPV) Type IIb. The ‘twin spotting’ phenomenon has been proposed in the pathogenesis of PPV, and PPV is an example of non... 
twin spotting | port‐wine stain | naevus of Ota | Mongolian spots | phakomatosis pigmentovascularis | Port-wine stain | Naevus of Ota | Phakomatosis pigmentovascularis | Twin spotting | port-wine stain | DERMATOLOGY | Neurocutaneous Syndromes - diagnosis | Diagnosis, Differential | Port-Wine Stain - pathology | Humans | Port-Wine Stain - diagnosis | Adult | Female | Neurocutaneous Syndromes - pathology | Melanosis - pathology | Melanosis - diagnosis
Journal Article
프로그램북(구 초록집), 2018, Volume 70, Issue 1, p. 483
Phakomatosis pigmentovascularis (PPV) can be classified by Classic Hasegawa's 5 types or new Happle's 4 types... 
Unclassifiable phakkomatosis | Phakomatosis pigmentovascularis
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 2010, Volume 66, Issue 2, pp. 341 - 342
... of the right eye. 11. What is the most likely diagnosis? a. Reticulate port wine stain b. Sturge–Weber syndrome c. Phakomatosis pigmentovascularis type V d. Macrocephaly... 
Dermatology | PHAKOMATOSIS-PIGMENTOVASCULARIS | MARMORATA TELANGIECTATICA CONGENITA | MONGOLIAN SPOTS | DERMATOLOGY | Skin
Journal Article
Journal of Clinical Ophthalmology and Research, ISSN 2320-3897, 01/2017, Volume 5, Issue 2, pp. 91 - 93
.... The coexistence of cutaneous hemangioma and pigmentary naevi is known as phakomatosis pigmentovascularis... 
phakomatosis pigmentovascularis | Sturge-Weber syndrome | Nevus of Ota
Journal Article
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