A case of phakomatosis pigmentovascularis association with congenital temporal alopecia / 대한피부과학회지
Korean Journal of Dermatology
;
: 252-255, 1991.
Article
in Korean
| WPRIM
| ID: wpr-110682
ABSTRACT
Phakomatosis pigmentovascularis is characterized by the coexistence of pigmentary and vascular nevi, which are occasionally associated with systemic organ involvement. We report a 12-year-old male, who showed bilateral nevus of Ota on the forehead, periorbital area, sclera and soft palate, nevus of Ito on the scapular area, mongolian spot on the sacral area and widespread nevus flammeus. He was also associated with congenital temporal alopecia on the lower portion of left temporal region since birth.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Palate, Soft
/
Sclera
/
Nevus of Ota
/
Port-Wine Stain
/
Neurocutaneous Syndromes
/
Parturition
/
Mongolian Spot
/
Alopecia
/
Forehead
/
Nevus
Limits:
Child
/
Humans
/
Male
Language:
Korean
Journal:
Korean Journal of Dermatology
Year:
1991
Type:
Article
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