TY  - BOOK
AU  - Hellman,Per
ED  - SpringerLink (Online service)
TI  - Primary Aldosteronism: Molecular Genetics, Endocrinology, and Translational Medicine 
SN  - 9781493905096
AV  - RB155-155.8 
U1  - 611.01816 23
PY  - 2014///
CY  - New York, NY
PB  - Springer New York, Imprint: Springer
KW  - Medicine
KW  - Human genetics
KW  - Endocrinology
KW  - Biomedicine
KW  - Human Genetics
KW  - Biomedicine general
KW  - Electronic books
KW  - local
N1  - Introduction -- Primary Aldosteronism: Molecular Mechanisms and Diagnosis -- Epidemiology and need for screening -- Low renin hypertension -- Molecular derangements in sporadic primary aldosteronism -- From genetic abnormalities to pathophysiological mechanisms -- Familial hyperaldosteronism type I -- Familial hyperaldosteronism type II -- Familial hyperaldosteronism type III -- The Aldosterone-renin ratio – role and problems -- Confirmatory testing for Primary Aldosteronism -- Radiological imaging of adrenocortical tumors -- Aldosterone and cardiovascular disease -- Quality of life aspects of primary aldosteronism -- Medical treatment of primary aldosteronism -- Surgical treatment of primary aldosteronism -- Index
N2  - Primary Aldosteronism (PA) is a disease caused by the overproduction of aldosterone hormone from the adrenal glands. PA causes hypertension and the majority with this disease are undiagnosed for PA. There are new insights into this matter by using biochemistry as well as advanced radiology. In 2011, a breakthrough in the genetic derangements came, identifying a mutated potassium channel gene – KCNJ5 – in about 40% of PA with adenoma. Chapters in this book include a history of the disorder, epidemiology, genetics derangements, the KCNJ5 mutations and phenotype and more
UR  - http://ezproxy.alfaisal.edu/login?url=http://dx.doi.org/10.1007/978-1-4939-0509-6
ER  -