1[1]Ota M, Kawamura T, Ito N. Phakomatosis Pigmentovascularis(Ota)[J]. Jpn J Dermatol, 1947,52:1-3.
2[2]Mahroughan M,Mehregan AH,Mehregan DA.Phakomatosis Pigmentovascularis:report of a case[J]. Pediatr Dermatol, 1996,13(1):36-38.
3[3]Hasegawa Y, Yasuhara M. Phakomatosis pigmentovascularis type Iva[J]. Arch Dermatol, 1985 ,121(5):651-655.
4[4]Uysal G, Guven A, zhan B,et al. Phakomatosis pigmentovascularis with Sturge-Weber syndrome: a case report[J]. J Dermatol, 2000, 27(7):467-470.
5[5]Ono I,Tateshita T.Phacomatosis pigmentovascularis type Iia successfully treated with two types of laser therapy[J].Br J Dermatol,2000,142(2): 358-361.
6Happle R. Phacomatosis pigmentovascularis revisited and reclassi-fied[J].{H}ARCHIVES OF DERMATOLOGY,2005,(03):385-388.
7Onsun N,Inandirici A,Kural Y. Phakomatosis pigmentovascu-laristypeIIb with bilateral hearing impairment[J].{H}Journal of the European Academy of Dermatology and Venereology,2007,(03):402-403.
8Adachi K,Togashi S. Laser therapy treatment of phacomatosis pigmentovascularis type II:two case reports[J].J Med Case Rep,2013,(01):55.
