Ehlers–Danlos syndrome in the practice of a therapist

DOI: https://doi.org/10.29296/25877305-2021-08-06
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Issue: 
8
Year: 
2021

Associate Professor O. Radaykina(1), Candidate of Medical Sciences; Professor E. Polozova(1),
MD; Associate Professor V. Skvortsov(2), MD; Professor A. Usanova(1), MD; Associate Professor I. Fazlova(1),
Candidate of Medical Sciences; Associate Professor N. Guranova(1), Candidate of Medical Sciences; E.
Radaykina(1) (1)Ogarev Mordovia State University, Saransk (2)Volgograd State Medical University

Ehlers–Danlos syndrome is a heterogeneous group of rare hereditary diseases, manifested by mesenchymal dysplasia, is determined by various pathologies in DNA regions encoding the structure of collagen, or DNA regions containing information about biologically active proteins involved in the processes of transformation of its fibers with skin lesions, musculoskeletal locomotor system and other organs. On the basis of research carried out in recent years, the clinical picture and diagnosis of all selected types of disease that may be encountered in the work of a general practitioner are considered.
Keywords: 
Ehlers-Danlos syndrome
genetic markers
mechanisms of development
clinical picture
diagnosis

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