Nevus anemicus associated with neurofibromatosis type 1 in a neonate: a case report.

Cerini, C; Pogliani, L; Mameli, C; Zuccotti, G V

Cerini, C; Pogliani, L; Mameli, C; Zuccotti, G V.

Affiliation

Cerini C; Department of Pediatrics, L. Sacco Hospital, University of Milan, Milan, Italy - gianvincenzo.zuccotti@unimi.it.

G Ital Dermatol Venereol ; 150(6): 745-7, 2015 Dec.

Article in En | MEDLINE | ID: mdl-26513044

Subject(s)

Neurofibromatosis 1/diagnosis; Nevus/congenital; Skin Neoplasms/congenital; Diagnosis, Differential; Early Diagnosis; Female; Frameshift Mutation; Genes, Neurofibromatosis 1; Humans; Hypopigmentation/congenital; Hypopigmentation/genetics; Infant, Newborn; Neurofibromatosis 1/genetics; Neurofibromatosis 1/pathology; Nevus/genetics; Skin Neoplasms/genetics; Thorax; Vitiligo/diagnosis

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Collection: 01-internacional Database: MEDLINE Main subject: Skin Neoplasms / Neurofibromatosis 1 / Nevus Type of study: Diagnostic_studies / Risk_factors_studies / Screening_studies Limits: Female / Humans / Newborn Language: En Journal: G Ital Dermatol Venereol Year: 2015 Document type: Article Country of publication: Italy

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