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Rare but not forgotten syndrome: Osteodystrophies Albright type A

https://doi.org/10.18705/2311-4495-2015-0-2-3-98-102

Abstract

The clinical case of a patient with hereditary osteodystrophy Albright type 1 A, characterized by peripheral resistance to different groups of hormones, is presented in this article. Some clinical implications, features of a course of a disease in this patient as well as the complexity of differential diagnostic search and the algorithm of differential diagnosis of endocrine pathology are described.

About the Authors

Anastasia S. Liskina
Federal Almazov North-West Medical Research Centre
Russian Federation


E. K. Kudrjashova
Federal Almazov North-West Medical Research Centre
Russian Federation


Irina Leonova Nikitina
Federal Almazov North-West Medical Research Centre
Russian Federation


References

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3. Phelan M. C., Rogers R. C., Clarkson K. B. et al. Albright hereditary osteodystrophy and del (2) (q37.3) in four unrelated individuals. Am J Med Genet.1995; 58(1): 1-7.

4. Spiegel A. M. The molecular basis of disorders caused by defects in G proteins. Horm Res.1997; 47(3): 89-96.

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Review

For citations:


Liskina A.S., Kudrjashova E.K., Nikitina I.L. Rare but not forgotten syndrome: Osteodystrophies Albright type A. Translational Medicine. 2015;(2-3):98-102. (In Russ.) https://doi.org/10.18705/2311-4495-2015-0-2-3-98-102

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ISSN 2311-4495 (Print)
ISSN 2410-5155 (Online)