Phakomatosis pigmentovascularis type IIIb

Journal of the American Academy of Dermatology

Volumn 29, Issue 2, 1993, Pages 305-307

  Libow, Lester F ^a  

^a NONE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANGIOOSTEOHYPERTROPHY SYNDROME; ARTICLE; CASE REPORT; CLINICAL FEATURE; FEMALE; HUMAN; NEVUS FLAMMEUS; PHAKOMATOSIS; PRIORITY JOURNAL;

ADULT; CASE REPORT; FEMALE; HAMARTOMA; HUMAN; NEOPLASMS, MULTIPLE PRIMARY; NEVUS, PIGMENTED; SKIN NEOPLASMS;

EID: 0027317663     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/0190-9622(93)70181-R     Document Type: Article

References (13)

1. Phacomatosis pigmentovas-cularis (Ota)
2. A new type of phacomatosis pigmentovascularis Ota
3. Phakomatosis pigmentovascularis type IVa
4. A variant of phacomatosis pigmentovascularis
5. Oculocutaneous melanosis associated with the Sturge-Weber syndrome
6. Sturge-Weber and Klippel-Trenaunay syndrome with nevus of Ota and Ito
7. Oligosymptomatic form of Klippel-Trenaunay-Weber syndrome associated with giant nevus spilus
8. A case of phacomatosis pigmentovascularis
9. Portwine stains: a disease of altered neural modulation of blood vessels
10. Melanogenesis in cultures of peripheral nervous tissue. I The original fate of cells giving rise to melanocytes
11. Multiple granular cell tumors associated with giant speckled lentiginous nevus and nevus fiammeus in a child
12. Pigmentovascular nevus
13. Klippel-Trenaunay and Sturge-Weber syndrome with extensive mongolian spots, hypoplastic larynx and subglottic stenosis