The search for candidate genes associated with hypermobile Ehlers-Danlos syndrome
Abstract
The results of a molecular genetic study of patients with a hypermobile type of Ehlers-Danlos syndrome (hEDS) are presented. A possible algorithm for verifying hEDS and other inherited disorders of connective tissue with unspecified etiology is proposed.
About the Authors
E. A. Serebryakova
D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology
Russian Federation
Russian Federation
T. I. Kadurina
North-Western State Medical University named after I.I. Mechnikov
Russian Federation
Russian Federation
L. R. Lonishin
Peter the Great St.Petersburg Polytechnic University
Russian Federation
Russian Federation
L. N. Abbakumova
North-Western State Medical University named after I.I. Mechnikov
Russian Federation
Russian Federation
Y. A. Barbitof
D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology
Russian Federation
Russian Federation
D. E. Polev
D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology
Russian Federation
Russian Federation
O. S. Glotov
D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology
Russian Federation
Russian Federation
A. S. Glotov
D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology
Russian Federation
Russian Federation
Review
For citations:
Serebryakova E.A., Kadurina T.I., Lonishin L.R., Abbakumova L.N., Barbitof Y.A., Polev D.E., Glotov O.S., Glotov A.S. The search for candidate genes associated with hypermobile Ehlers-Danlos syndrome. Medical Genetics. 2020;19(8):54-56. (In Russ.)
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