Zobrazeno 1 - 2
of 2
pro vyhledávání: '"А. N. Semyachkina"'
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 66, Iss 2, Pp 101-104 (2021)
Hereditary connective tissue diseases are among the most common genetic syndromes. In most cases the studies of children with Ehlers–Danlos syndrome are devoted to the clinical manifestations of the disease. Insufficient information on the features
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 65, Iss 6, Pp 84-90 (2021)
The Ehlers-Danlos syndrome is a rare (orphan) disease characterized by the connective tissue dysplasia, fragility of the blood vessels and tissues, and variable clinical pattern. The vascular type of Ehlers-Danlos syndrome, which belongs to Group A a