scholarly journals Leydig cell ovarian tumor – clinical case description and literature review

2020 ◽  
Vol 19 (3) ◽  
pp. 140-143
Author(s):  
Mateusz Klimek ◽  
Patrycja Radosz ◽  
Magdalena Lemm ◽  
Wojciech Szanecki ◽  
Aleksandra Dudek ◽  
...  
Keyword(s):  
Literature Review ◽  
Leydig Cell ◽  
Ovarian Tumor ◽  
Clinical Case ◽  
Case Description

Features of redox homeostasis in patients with liver cirrhosis (literature review and clinical case description)

2020 ◽  
Vol 26 (1) ◽  
pp. 70-86
Author(s):  
M.O. Abrahamovych ◽  
◽  
O.O. Abrahamovych ◽  
O.P. Fayura ◽  
L.R. Fayura ◽  
...  
Keyword(s):  
Liver Cirrhosis ◽  
Literature Review ◽  
Clinical Case ◽  
Redox Homeostasis ◽  
Case Description

scholarly journals Risk Factors of Ischemic Stroke in Children with Head and Neck Tumors: A Clinical Case Description with a Literature Review

2021 ◽  
Vol 7 (3) ◽  
pp. 163
Author(s):  
Anastasia D. Rodina ◽  
Vladimir Sh. Vanesyan ◽  
Tatiana V. Gorbunova ◽  
Natalia V. Ivanova ◽  
Vladimir G. Polyakov
Keyword(s):  
Risk Factors ◽  
Ischemic Stroke ◽  
Literature Review ◽  
Head And Neck ◽  
Clinical Case ◽  
Head And Neck Tumors ◽  
Case Description ◽  
Neck Tumors

scholarly journals New-Onset Refractory Status Epilepticus (NORSE): literature review and clinical case description

2020 ◽  
Vol 12 (3) ◽  
pp. 169-176
Author(s):  
S. G. Burd ◽  
M. B. Mironov ◽  
E. R. Moizykevich ◽  
Yu. V. Rubleva ◽  
M. A. Bogomazova ◽  
...  
Keyword(s):  
Status Epilepticus ◽  
Literature Review ◽  
Clinical Case ◽  
Refractory Status Epilepticus ◽  
Case Description ◽  
Refractory Status ◽  
New Onset

scholarly journals Cardiotoxicity of Chemotherapeutic Drugs (Literature Review and Clinical Case Description)

2019 ◽  
Vol 4 (28) ◽  
pp. 51-61
Author(s):  
Ashot A. Avagimyan ◽  
◽  
Lusine G. Mkrtchyan ◽  
Keyword(s):  
Literature Review ◽  
Clinical Case ◽  
Case Description ◽  
Chemotherapeutic Drugs

scholarly journals Loeys–Dietz syndrome (literature review and case description)

2020 ◽  
Vol 8 (1) ◽  
pp. 83-94
Author(s):  
Olga E. Agranovich ◽  
Sergey Yu. Semenov ◽  
Eugeniya F. Mikiashvili ◽  
Svetlana V. Sarantseva
Keyword(s):  
Differential Diagnosis ◽  
Connective Tissue ◽  
Literature Review ◽  
Clinical Case ◽  
Multidisciplinary Approach ◽  
Clinical Observation ◽  
Autosomal Dominant ◽  
Connective Tissue Disorder ◽  
Dynamic Monitoring ◽  
Case Description

Background. The LoeysDietz syndrome is a rare autosomal dominant connective tissue disorder characterized by the pathology of the cardiovascular system in combination with various anomalies of the musculoskeletal system. In modern literature, there is neither any information about the frequency of pathology nor any algorithm of examination and treatment for patients with this syndrome. Clinical case. The article presents a clinical observation of a 7-year-old patient with LoeysDietz syndrome with a genetically confirmed diagnosis. Discussion. This article provided a literature review, examined diagnosis issues and differential diagnosis, and presented the clinical picture of the syndrome. The main symptoms of LoeysDietz syndrome are artery aneurysms (most often in the aortic root), arterial tortuosity (mainly the vessels of the neck), hypertelorism, and bifid (split) or broad uvula. However, the combination of these symptoms is not found in all patients with this disease. Conclusions. The article emphasized the importance of a genetic verification of the disease, as well as a multidisciplinary approach to treatment with mandatory dynamic monitoring by specialists such as a cardiologist, neurologist, orthopedist, and pediatrician, which help prevent the development of complications and increase the life expectancy of this group of patients.

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