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Hypertension
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Hypertension

Clinical feature: 

Definition: The disease is defined by elevated systolic or diastolic blood pressure that is associated with increased risk for cardiovascular and renal disease. The disease might be primary, genetically determined or secondary to renal, edocrinological or neurological diseases.

Pathogenesis: Pathogenetic aspects of primary hypertension can be divided into three groups: monogenic forms of hereditary hypertension. mutations and polymorphisms associated with increased risk of hypertension. genetic variations responsible for increased susceptibility to hypertensive complications.

Clinical picture: In most cases hypertension is asymptomatic when recognized. Patients rather start complaining when blood pressure is lowered too abruptly. Family history, however, reveals several members with not only elevated blood pressure but also stroke and other cardiovascular diseases resulting from untreated hypertension.

Diagnostics: 

Strategy: First, a secondary hypertension has to be excluded. Next, it should be proved if there were signs of some monogenic form of hypertension. Last, genetic risks have to be evaluated.

Systematic link table: 

Hereditary diseases
HIV resistance
CCR5
Hereditary bone disease
Hereditary endocrinological diseases
Hereditary kidney diseases
Hereditary metabolic diseases
Hereditary neurological disorders
Hereditary ocular disease and visual impairment
Hereditary vascular disease
Hypertension
ACE
ACE2
AGT
Monogenic hypertension
Apparent mineralocorticoid excess
HSD11B2
Glucocorticoid-remediable aldosteronism
CYP11B1
CYP11B2
Liddle syndrome
NEDD4
NEDD4L
NR3C2
SCNN1B
SCNN1G
Pseudohypoaldosteronism
Pseudohypoaldosteronism type 2
WNK1
WNK4
Pseudohypoaldosteronism type1
NR3C2
SCNN1A
SCNN1B
SCNN1G
hereditary diseases of the hematopoetic system and coagulopathies

Literature: 

Freedman BI et al. (2003) Susceptibility genes for hypertension and renal failure.
Barlassina C et al. (2002) Genetics of essential hypertension: from families to genes.