Objective: to establish clinical and epidemiological features in chidren with various forms of short stature (SS) in the Odessa region. Methods. The work was conducted at the Outpatient Department of the Odessa Regional ...

Purpose of the study was in the analysis of clinical features, diagnostic and therapeutic tactics, as well as prognostic assessment of various forms and stages of the course of associated craniocerebral injuries in ...

Epilepsy is a dangerous pathology, which if not treated in time, epileptic seizures become more aggressive and can result in a tragic end - the patient becomes disabled or dies. The principal cause of epilepsy in children ...

Primary hepatic pregnancy is an extremely rare nozological entity, with unique cases reported in the specialized literature. This can be defined as implantation on the liver of the fertilized egg, a fact favored by the ...

Behcet’s disease is a multisystemic disease of unknown etiology. Behcet’s disease is named after the Turkish dermatologist Hulusi Behçet, who in 1937 described a syndrome of recurrent foot-and-mouth disease, genital ulcers, ...

Introduction: The new nosological entity –COVID-19, is a real challenge for the health system around the whole world. In terms of viral tropism, the heart and vessels are also involved in the pathological process. Purpose: ...

Estimating the effectiveness of the vaccine helps to shape a true overview of the benefits of immunization, thus facilitating the global promotion of vaccine prophylaxis. Streptococcus pneumoniae is the most common pathogen ...

Background. High blood pressure is a multifactorial disease, in the realization of which several pathogenetic links are involved, however they are insufficiently elucidated in the pediatric population. The material and ...

Introduction. As a consequence of the chronic inflammatory process, children with rheumatic conditions can present with both - variable degree of joint pain and limitation of the range of motion, the last one, sometimes ...

Bartter syndrome is a rare primary hereditary tubulopathy with an autosomal recessive transmission mechanism affecting the absorption of salts in the ascending segment of the Henle loop, manifested by hypokalemia, ...