A Case of Pasqualini Syndrome
Journal Title: Міжнародний ендокринологічний журнал - Year 2016, Vol 4, Issue 76
Abstract
The article presents a case of isolated congenital deficiency of luteinizing hormone (Pasqualini syndrome) that manifested by secondary hypogonadism with abnormalities of copulative and fertile functions, which were normalized after the treatment using chorionic gonadotropin.
Authors and Affiliations
P. M. Liashuk, R. P. Liashuk
Efficiency and Safety of Metformine and Pioglitazone in Patients with Coronary Heart Disease and Diabetes Mellitus Type 2
A combination of metformin (MF) (2 g daily) and pioglitazone (PG) (30 mg daily) in 57 patients with coronary heart disease (CHD) and diabetes mellitus type 2 (DM 2) reduces the indicators of low grade chronic inflammatio...
Violations of the System of Lipid Peroxidation in Type 2 Diabetes Mellitus (Literature Review)
The review presents the data on the current state of the problem of diabetes mellitus type 2 and the role of oxidative stress. Over the last decade, the number of patients with diabetes mellitus has increased by more tha...
Allergenspecific Immunotherapy: History, Current Views and Problems
As you know, the most common form of allergic reactions is the so-called IgE-mediated hypersensitivity, which, according to various authors, occurs in 25 % of the population of industrialized countries [1]. It is commonl...
Adrenal Hyperandrogenism: Multidisciplinary Approach to Solving Problemss
Prevalence and possible consequences of the hyperandrogenic states in women of reproductive age stipulate the importance of timely differential diagnosis of hyperandrogenism. Taking into account the level of the developm...
Impact of Nonselective Laryngeal Reinnervation on Main Voice Characteristics
The possibility and long-term results of non-selective surgical reinnervation by primary and delayed anastomosis of recurrent laryngeal nerve (RLN) with the one of the peripheral neck nerve (proximal RLN part, main part...