Zobrazeno 1 - 10
of 589
pro vyhledávání: '"von recklinghausen's disease"'
Autor:
Akihiko Ueda, Kenta Saito, Hiromichi Murase, Tomokatsu Kato, Hiroyuki Imafuji, Mamoru Morimoto, Ryo Ogawa, Hiroki Takahashi, Yoichi Matsuo, Shuji Takiguchi
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-6 (2024)
Abstract Background Neurofibromatosis type 1 is an autosomal-dominant disease characterized by café-au-lait spots and neurofibromas, as well as various other symptoms in the bones, eyes, and nervous system. Due to its connection with vascular fragil
Externí odkaz:
https://doaj.org/article/2f8256cf649b4403a648db2b8018ee73
Autor:
Reza Jahanshahi, Fatemeh Mirzaei, Mohammad Hossein Askari, Nafiseh Asgari, Shohreh Ghasemi, Akram Sanagoo, Leila Jouybari
Publikováno v:
Journal of Research Development in Nursing and Midwifery, Vol 20, Iss 2, Pp 63-66 (2023)
Background: Because of the numerous problems created by neurofibromatosis type 1, particular quality-of-life evaluation measures are quite significant. In Iran, general instruments are used to assess the quality of life of the target group. This stud
Externí odkaz:
https://doaj.org/article/c288e2e69c784036a1144bd757d17cd5
Autor:
Reza Jahanshahi, Zahra Yasaghi, Fatemeh Mirzaei, Shohreh Ghasemi, Akram Sanagoo, Leila Jouybari, Samira Foji
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-6 (2023)
Abstract Background The notion of “burden” has taken a key place in the evaluation of care, particularly in the case of rare diseases. The aim of this study was to evaluate the psychometric properties of the burden of neurofibromatosis 1 question
Externí odkaz:
https://doaj.org/article/8414fe4d02b74d1fa758cdc791af8f30
Autor:
C. Muhizi, H. Irere, B. Tuyishimire, A. Ndatinya, O. R. Karangwa, F. Rutagarama, C. Nsanzabaganwa, L. Mutesa
Publikováno v:
Rwanda Medical Journal, Vol 79, Iss 4, Pp 5-8 (2022)
INTRODUCTION: Neurofibromatosis Type 1 (NF1) or Von Recklinghausen’s disease, is a rare genetic disease characterized by multiple benign tumors of nerves and skin (neurofibromas), and skin decorations. However, it is multisystem and can affect each
Externí odkaz:
https://doaj.org/article/8bc1a5d5c5714643bd41121dc910d626
Akademický článek
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Akademický článek
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Autor:
V. Hadzhiminev
Publikováno v:
Trakia Journal of Sciences, Vol 19, Iss 2, Pp 200-204 (2021)
Secondary spontaneous pneumothorax (SSP) may be a result of different rare diseases. In the following article are presented two interesting cases of SSP related to genetic disorders – Ehlers-Danlos syndrome (EDS) and Neurofibromatosis type 1 (NF-1)
Externí odkaz:
https://doaj.org/article/e65a14b8fa564b76b2a032ebdeb1b0b5
Autor:
Ali Baradaran Bagheri, Sepehr Aghajanian, Aliasghar Taghi Doulabi, Mehdi Chavoshi-Nejad, Somayeh Sorouredin Abadi
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Spinal neurofibromatosis (SNF) is a rare form of Neurofibromatosis in which neurofibromas exist bilaterally throughout all spinal roots. Despite previous attempts made to characterize and classify the disease as a separate clinical form of the diseas
Externí odkaz:
https://doaj.org/article/e1dc7f63abe74d25a62dd46be83ef909
Autor:
Yusoon Kim, Kazuhiro Yagihara, Jun Sumino, Miki Katsurano, Mari Shibata, Koichi Kadoya, Ayataka Ishikawa
Publikováno v:
Oral and Maxillofacial Surgery Cases, Vol 8, Iss 2, Pp 100255- (2022)
von Recklinghausen's disease (vRD) is an autosomal dominant neurogenetic disorder characterized by symptoms of neurofibroma and café-au-lait plaques. Although some nonepithelial tumors, such as malignant peripheral nerve sheath tumors and optic nerv
Externí odkaz:
https://doaj.org/article/c0899de4ca624242928b5446a5f03ce8
Autor:
Daniel Wolder, Adrian Swat
Publikováno v:
Journal of Education, Health and Sport, Vol 12, Iss 2 (2022)
Neurofibromatosis is a genetic disease inherited in an autosomal, dominant manner. The course of von Recklinghausen’s disease varies from patient to patient. Most cases are mild and uncomplicated. The diagnosis of NF1 is based on the criteria of th
Externí odkaz:
https://doaj.org/article/0eba41aee10942f0b0348e53530a4b82