| Autor: |
Orciulo GV; graorc@gmail.com., Grasso D; daniela.grasso@hotmail.it., Borreggine C; carmela.borreggine@gmail.com., Castorani G; giulia.castorani90@gmail.com., Vergara D; dorianavergara@hotmail.it., Nasuto M; michelangelo.nasuto@gmail.com., Ciccarese G; gcicca@yahoo.it., Popolizio T; t.popolizio1@gmail.com., Serricchio E; e.serricchio@operapadrepio.it., Guglielmi G; giuseppe.guglielmi@unifg.it. |
| Jazyk: |
angličtina |
| Zdroj: |
Acta bio-medica : Atenei Parmensis [Acta Biomed] 2022 Oct 14; Vol. 93 (S1), pp. e2022091. Date of Electronic Publication: 2022 Oct 14. |
| DOI: |
10.23750/abm.v93iS1.13059 |
| Abstrakt: |
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder with multisystemic involvement, affecting central nervous system, skin, bone system and vessels, with a very heterogeneous clinical presentation. Vascular abnormalities are typically recognized in neurofibromatosis type 1 affecting cardiovascular and cerebrovascular systems. The incidence of circle of Willis anomalies in children with NF1 is twofold higher than in general population. In this paper, we report of 19-years-old female with NF1 and twig-like middle cerebral artery. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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