Autosomal dominant hypertension with brachydactyly: An enigmatic form of monogenic hypertension

Nephrology Dialysis Transplantation

Volumn 13, Issue 6, 1998, Pages 1337-1340

  Schuster, Herbert ^a,b  

^a HUMBOLDT UNIVERSITY   (Germany)

^b FRANZ VOLHARD CLINIC   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BRACHYDACTYLY; HEREDITARY HYPERTENSION; MOLECULAR CLONING; PHENOTYPE; PRIORITY JOURNAL; SHORT SURVEY; ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL DOMINANT HYPERTENSION WITH BRACHYDACTYLY; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 12; CHROMOSOME 8; ESSENTIAL HYPERTENSION; GENE MAPPING; GENE MUTATION; HUMAN; HYPERTENSION; LIDDLE SYNDROME; MEAN ARTERIAL PRESSURE; MICROSATELLITE MARKER; MONOGENIC DISORDER; MONOGENIC HYPERTENSION; POSTERIOR INFERIOR CEREBELLAR ARTERY;

11BETA HYDROXYSTEROID DEHYDROGENASE; ALDOSTERONE SYNTHASE; ALPHA ADRENERGIC RECEPTOR BLOCKING AGENT; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CALCIUM ANTAGONIST; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; MINERALOCORTICOID RECEPTOR; MOXONIDINE; PLACEBO; STEROID 11BETA MONOOXYGENASE; THIAZIDE DIURETIC AGENT;

EID: 0031748626     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/13.6.1337     Document Type: Short Survey

References (10)

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