In:
Revista Científica Multidisciplinar Núcleo do Conhecimento, Revista Cientifica Multidisciplinar Nucleo Do Conhecimento
Abstract:
Xeroderma pigmentosum (XP) is a rare genetic disease, of autosomal and recessive character, and may affect both sexes, regardless of race, and often one case per 250,000 people. This disease has several other symptoms that present themselves heterogeneously over its carriers. The aim of this article was to quantitatively analyze the presence of the topic Xeroderma pigmentoso in scientific articles published between 2003 and 2018. In the identification, a total of 674 results were obtained. The follow-up of the following steps allowed, in the end, the selection of 24 papers. Regarding the language, most of the selected papers were written in Portuguese (around 58.33%), the rest in English (around 41.67%). The highest publication rates occurred between 2015 and 2017 (13%). The years 2007, 2007, 2011, 2014 and 2018 presented intermediate rates (9%) and the lowest rates (4%) occurred in 2003, 2008, 2010 and 2012, and 75% papers were published/presented in the 2nd decade of the 21st century, while the others (25%) were in the 1st decade of the 21st century. The findings of this study showed that there are few scientific studies on XP because it is a rare disease, which possibly leads to few investments in this area, especially with regard to treatment and medications.
Type of Medium:
Online Resource
ISSN:
2448-0959
DOI:
10.32749/nucleodoconhecimento
DOI:
10.32749/nucleodoconhecimento.com.br/health/topic-xeroderma
Language:
Portuguese
Publisher:
Revista Cientifica Multidisciplinar Nucleo Do Conhecimento
Publication Date:
2020