Academic Journal

Nijmegen breakage Syndrome - how much do we know about this rare condition of Slavs? - disease overview

التفاصيل البيبلوغرافية
العنوان: Nijmegen breakage Syndrome - how much do we know about this rare condition of Slavs? - disease overview
المؤلفون: Adrianna Muciek, Martyna Mocarska, Anna Orłowska, Katarzyna Strakowska, Laura Opalska, Anna Maryńczak, Jan Mencel, Nicole Nitschke
المصدر: Quality in Sport, Vol 34 (2024)
بيانات النشر: Nicolaus Copernicus University in Toruń, 2024.
سنة النشر: 2024
المجموعة: LCC:Sports
LCC:Sports medicine
مصطلحات موضوعية: Nijmegen breakage syndrome, chromosome instability, immunodeficiency, Sports, GV557-1198.995, Sports medicine, RC1200-1245
الوصف: Nijmegen breakage syndrome (NBS) is a rare autosomal recessive defect of immunity, characterised by chromosomal instability and radiation sensitivity with a high predisposition to malignancy. The clinical manifestations of this condition include microcephaly, combined immunodeficiency, growth retardation and a range of additional abnormalities, including facial, skeletal and skin anomalies (such as café au lait spots and vitiligo). It is estimated that 40% of patients will develop cancer before reaching the age of 21 years. [1-2] The aetiology of this syndrome can be attributed to a mutation in the NBS1 gene, which is localised on chromosome 8q21 and is responsible for the production of the protein nibrin. [3] The most common mutation responsible for NBS (c.657_661del5) is consistent with a founder effect, with the majority of registered patients originating from Central and Eastern Europe and the largest cohort diagnosed in Poland. [4] This article provides an overview of Nijmegen breakage syndrome (NBS), including epidemiology, symptoms, diagnostic pathway and patient management, as well as treatment options. The objective of this study is to enhance awareness of this condition in order facilitate an early diagnosis and screening for malignancy in patients.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2450-3118
Relation: https://apcz.umk.pl/QS/article/view/56216; https://doaj.org/toc/2450-3118
DOI: 10.12775/QS.2024.34.56216
URL الوصول: https://doaj.org/article/42c2a8ef0ece44578b7b0749962d5c47
رقم الانضمام: edsdoj.42c2a8ef0ece44578b7b0749962d5c47
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:24503118
DOI:10.12775/QS.2024.34.56216