Diagnostic and therapeutic process of neurofibromatosis type 1 and type 2

Neurofibromatosis is one of the most common genetic diseases. It is inherited in an autosomal dominant manner. It is divided into two genetically distinct subtypes, characterised by multiple skin lesions and tumours of the peripheral and central nervous system. Neurofibromatosis   type   1,   or...

Volledige beschrijving

Bibliografische gegevens
Hoofdauteurs: Michał Leśniewski, Iwona Welian-Polus, Izabela Oleksak, Karolina Maliszewska
Formaat: Artikel
Taal:English
Gepubliceerd in: Kazimierz Wielki University 2024-02-01
Reeks:Journal of Education, Health and Sport
Onderwerpen:
Online toegang:https://apcz.umk.pl/JEHS/article/view/48531

Gelijkaardige items