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Archives of Pediatrics and Adolescent Medicine

Volumn 155, Issue 2, 2001, Pages 191-192

  Narchi, Hassib ^a,b   Santos, Marissa ^a   Tunnessen Jr , Walter W ^a  

^a Saudi Aramco Al Hasa Health Center   (Saudi Arabia)

^b SANDWELL GENERAL HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOOSTEOHYPERTROPHY SYNDROME; ARTICLE; CASE REPORT; CHROMOSOME MUTATION; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; HUMAN; INFANT; MALE; NEVUS FLAMMEUS; PATHOGENESIS; PHAKOMATOSIS PIGMENTOVASCULARIS; PRIORITY JOURNAL; STURGE WEBER SYNDROME; VASCULAR LESION; DIFFERENTIAL DIAGNOSIS; PHAKOMATOSIS;

DIAGNOSIS, DIFFERENTIAL; HUMANS; INFANT; MALE; NEUROCUTANEOUS SYNDROMES; PORT-WINE STAIN; STURGE-WEBER SYNDROME;

EID: 0035146774     PISSN: 10724710     EISSN: None     Source Type: Journal    
DOI: 10.1001/archpedi.155.2.191     Document Type: Article

References (6)

1. Phakomatosis pigmentovascularis: A new case with renal angiomas and some considerations about the classification
2. Phacomatosis pigmentovascularis type II
3. Glaucoma in phakomatosis pigmentovascularis
4. Multiple granular cell tumors associated with giant speckled lentiginous nevus and nevus flammeus in a child
5. Phacomatosis pigmentokeratotica: Report of new cases and further delineation of the syndrome
6. Allelics somatic mutations may explain vascular twin nevi