1283 Somatic GNAQ mutation in different structures of Port-wine Macrocheilia
نویسندگان
چکیده
منابع مشابه
Sturge–Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
From the Biochemistry, Cellular and Molecular Biology Program (M.D.S., J.D.B., J.P.) and the Departments of Dermatology (B.C.), Neurology (A.M.C.), Pediatrics (A.M.C.), and Psychiatry and Behavioral Sciences (J.P.), Johns Hopkins School of Medicine, and the Department of Neurology and Developmental Medicine, Hugo W. Moser Research Institute at Kennedy Krieger (M.D.S., J.D.B., L.P.F., A.M.C., J....
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Acquired port-wine stain is a rare vascular lesion that mimics a congenital port-wine stain clinically and histologically, but is acquired after birth. A survey on more than 60 reported cases in the literature reveals that most of these cases are idiopathic, but some of the cases developed after physical or mechanical trauma, hormonal changes, chronic sun exposure, and medications (OCP, i...
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Port wine stains are benign but cosmetically devasting congenital angiomas. The argon laser is a therapeutic device newly applied to this condition. Our program was begun 6 years ago. From the beginning, the study was conceived as a clinical investigation of both the port wine stain and its argon laser therapy. A total of 218 patients with port wine stains have been studied and many aspects of ...
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BACKGROUND Recent reports have proposed that there were no differences between acquired port-wine stain (APWS) and congenital port-wine stain (CPWS) except the onset of disease. Pulsed dye laser (PDL) therapy is regarded as the treatment of choice in PWS. Although in some articles, APWS might have shown a better response to PDL than CPWS, this is still controversial. It has been assumed however...
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ژورنال
عنوان ژورنال: Journal of Investigative Dermatology
سال: 2018
ISSN: 0022-202X
DOI: 10.1016/j.jid.2018.03.1299