scholarly journals Undifferentiated connective tissue dysplasia in dermatological and cosmetological practice (clinical case)

2019 ◽  
Vol 2 (26) ◽  
pp. 29-33
Author(s):  
E. V. Ikonnikova ◽  
A. G. Stenko ◽  
L. S. Kruglova

The article presents a case of clinical observation of a patient with connective tissue dysplasia. This pathology, as a result of various genetic disorders, includes an extensive group of different systemic conditions, most of which have certain dermatological pathologies as the main or concomitant symptom. We describe the questions of etiology, clinic and diagnosis of connective tissue dysplasia. This clinical case is interesting to practicing dermatologists and cosmetologists in connection with the high appeal of this category of patients for aesthetic help.

2019 ◽  
Vol 8 (3) ◽  
pp. 130-135
Author(s):  
L. N. Igisheva ◽  
A. A. Anikeenko ◽  
R. A. Kornelyuk ◽  
М. V. Kulavskaya ◽  
N. G. Perevalova

Medical records of a patient presented with severe aortic and mitral regurgitation and connective tissue dysplasia were reviewed. Clinical, laboratory and instrumental findings were collected at baseline and after the surgery. Long-term outcomes, including quality of life, were estimated.


2016 ◽  
Vol 11 (2) ◽  
Author(s):  
Galina Nechaeva ◽  
Olga Drokina ◽  
Vitaliy Ochlopkov ◽  
Alexey Kononov ◽  
Vladimir Konev ◽  
...  

2020 ◽  
Vol 8 (1) ◽  
pp. 83-94
Author(s):  
Olga E. Agranovich ◽  
Sergey Yu. Semenov ◽  
Eugeniya F. Mikiashvili ◽  
Svetlana V. Sarantseva

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.


We present a clinical case of a wrong diagnosis of myasthenia in a patient with incomplete ptosis slowly progressing for 5 years, which, by its isolation and asymmetry, imitated ocular symptomatology in myasthenia. The clinical picture was not consistent with the diagnostic criteria for myasthenia. Moreover, other pathology according to laboratory and instrumental studies was absent. There was observed a combination of signs of connective tissue dysplasia in the heart in the form of valve syndrome, skeletal abnormalities, eye pathology syndrome, which made it possible to diagnose the syndrome of undiff erentiated connective tissue dysplasia. Diffi culties in the diff erential diagnosis were polysystemic lesions, the absence of pathognomonic tests for the detection of connective tissue dysplasia, and features of a diff erential diagnosis with ocular myasthenia gravis.


Author(s):  
N.S. Beganskaya ◽  
V.V. Anikin ◽  
O.A. Izvarina ◽  
T.O. Nikolaeva ◽  
A.D. Kozhevnikova

2020 ◽  
pp. 61-63
Author(s):  
S. Sh. Kakvaeva ◽  
M. A. Magomedova ◽  
A. N. Dzhalilova

One of the most serious problems of modern medicine is sepsis. The number of patients undergoing this complication is 20–30 million (WHO) annually and has no tendency to decrease. Sepsis is characterized by severe multiple organ failure due to a violation of the response of the macroorganism to an infectious agent. Moreover, it is dangerous with high mortality. Sepsis often develops in patients with immunodeficiency conditions, which primarily include pregnant women. The article presents a clinical observation of a case of periostitis in a pregnant woman complicated by a septic state.


2016 ◽  
Vol 73 (1) ◽  
pp. 131-136 ◽  
Author(s):  
S.L. Nyan'kovskyi ◽  
◽  
O.O. Dobrik ◽  
M.Yu. Іs'kiv ◽  
◽  
...  

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