Neurofibromatosis type 1 (NF-1), or von Recklinghausen’s disease, is an autosomal dominant condition with an incidence of 1:3000 and a prevalence of 1:4000 to 1:5000. It is caused by a decrease in the production of the neurofibromin protein due to mutations in the NF1 gene, located on the long arm of chromosome 17 (17q11.2), resulting in a lack of control of cell growth and division
Nevus anemicus in neurofibromatosis type 1 / Miraglia, Emanuele; Iacovino, Chiara; Calvieri, Stefano; Giustini, Sandra. - In: ITALIAN JOURNAL OF DERMATOLOGY AND VENEREOLOGY. - ISSN 2784-8450. - 156:Suppl. 1 to No. 6(2021), pp. 103-104. [10.23736/S2784-8671.20.06491-3]
Nevus anemicus in neurofibromatosis type 1
Miraglia, Emanuele
;Iacovino, Chiara;Calvieri, Stefano;Giustini, Sandra
2021
Abstract
Neurofibromatosis type 1 (NF-1), or von Recklinghausen’s disease, is an autosomal dominant condition with an incidence of 1:3000 and a prevalence of 1:4000 to 1:5000. It is caused by a decrease in the production of the neurofibromin protein due to mutations in the NF1 gene, located on the long arm of chromosome 17 (17q11.2), resulting in a lack of control of cell growth and division| File | Dimensione | Formato | |
|---|---|---|---|
|
Miraglia_Nevus_2021.pdf
solo gestori archivio
Note: lettera all'editore
Tipologia:
Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza:
Tutti i diritti riservati (All rights reserved)
Dimensione
770.27 kB
Formato
Adobe PDF
|
770.27 kB | Adobe PDF | Contatta l'autore |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
