Donate Help Contact The AHA Sign In Home
American Heart Association
Hypertension
Search: search_blue_button Advanced Search
Hypertension. 1996;28:1085-1092

This Article
Right arrow Full Text
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Schuster, H.
Right arrow Articles by Luft, F. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schuster, H.
Right arrow Articles by Luft, F. C.

(Hypertension. 1996;28:1085-1092.)
© 1996 American Heart Association, Inc.


Articles

Autosomal Dominant Hypertension and Brachydactyly in a Turkish Kindred Resembles Essential Hypertension

Herbert Schuster; Thomas F. Wienker; Hakan R. Toka; Sylvia Bahring; Eva Jeschke; Okan Toka; Andreas Busjahn; Albrecht Hempel; Christoph Tahlhammer; Wolfgang Oelkers; Jurgen Kunze; Nihat Bilginturan; Hermann Haller; Friedrich C. Luft

The Clinical Research Unit, Max Delbruck Center for Molecular Medicine, Franz Volhard Clinic, Virchow Klinikum, Humboldt University of Berlin (Germany), and Section of Pediatric Endocrinology, Department of Pediatrics, Hacettepe University School of Medicine, Ankara, Turkey.

Correspondence to Friedrich C. Luft, Franz Volhard Clinic, Wiltberg Strasse 50, 13122 Berlin, FRG.

We examined a Turkish kindred with a unique form of autosomal dominant hypertension that cosegregates 100% with brachydactyly and maps to chromosome 12p. Affected adults were 10 to 15 cm shorter than unaffected people; however, their body mass index (27 kg/m2) was not different. Blood pressure increased steeply with age in the affected people so that by age 40 years, they had a mean blood pressure of 140 mm Hg, compared with 92 mm Hg in unaffected individuals. Complete clinical, roentgenographic, and laboratory evaluation was performed in 6 subjects, including 24-hour blood pressure measurements and humoral determinations before and after volume expansion with 2 L normal saline over 4 hours followed by volume contraction on the following day with a 20-mmol sodium diet and 40 mg furosemide at 8 AM, noon, and 4 PM. Two affected men aged 46 and 31 years; 3 affected women aged 40, 31, and 30 years; and 1 unaffected man aged 29 years were studied. Systolic pressures ranged from 170 to 250 mm Hg, and diastolic pressures ranged from 100 to 150 mm Hg in affected people; the unaffected man had a blood pressure of 120/70 mm Hg. Thyroid, adrenal, and renal functions were normal; electrolyte and acid-base statuses were normal. Calcium and phosphate homeostasis was normal. Day-night circadian blood pressure rhythm was preserved. The subjects were not salt sensitive; renin, aldosterone, and catecholamine values reacted appropriately to volume expansion and contraction. Affected people had mild cardiac hypertrophy and increased radial artery wall thickness. Fibroblasts from affected people grew more rapidly in culture than from unaffected people. We conclude that this novel form of inherited hypertension resembles essential hypertension.


Key Words: hypertension, genetic • sodium • compliance • echocardiography • growth substances




This article has been cited by other articles:


Home page
Arch NeurolHome page
S. T. Turner, M. Fornage, C. R. Jack Jr, T. H. Mosley, D. S. Knopman, S. L. R. Kardia, E. Boerwinkle, and M. de Andrade
Genomic Susceptibility Loci for Brain Atrophy, Ventricular Volume, and Leukoaraiosis in Hypertensive Sibships
Arch Neurol, July 1, 2009; 66(7): 847 - 857.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
S. Bahring, M. Kann, Y. Neuenfeld, M. Gong, D. Chitayat, H. R. Toka, O. Toka, G. Plessis, P. Maass, A. Rauch, et al.
Inversion Region for Hypertension and Brachydactyly on Chromosome 12p Features Multiple Splicing and Noncoding RNA
Hypertension, February 1, 2008; 51(2): 426 - 431.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
S. Bahring, A. Rauch, O. Toka, C. Schroeder, C. Hesse, H. Siedler, G. Fesus, W. E. Haefeli, A. Busjahn, A. Aydin, et al.
Autosomal-Dominant Hypertension With Type E Brachydactyly Is Caused by Rearrangement on the Short Arm of Chromosome 12
Hypertension, February 1, 2004; 43(2): 471 - 476.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
F. C. Luft, O. Toka, H. R. Toka, J. Jordan, and S. Bahring
Mendelian hypertension with brachydactyly as a molecular genetic lesson in regulatory physiology
Am J Physiol Regulatory Integrative Comp Physiol, October 1, 2003; 285(4): R709 - R714.
[Abstract] [Full Text] [PDF]


Home page
Clin Med ResHome page
F. C. Luft
Mendelian Forms of Human Hypertension and Mechanisms of Disease
Clin. Med. Res., October 1, 2003; 1(4): 291 - 300.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
M. Gong, H. Zhang, H. Schulz, Y.-A. Lee, K. Sun, S. Bahring, F. C. Luft, P. Nurnberg, A. Reis, K. Rohde, et al.
Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p
Hum. Mol. Genet., June 1, 2003; 12(11): 1273 - 1277.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
T. Ketch, I. Biaggioni, R. Robertson, and D. Robertson
Four Faces of Baroreflex Failure: Hypertensive Crisis, Volatile Hypertension, Orthostatic Tachycardia, and Malignant Vagotonia
Circulation, May 28, 2002; 105(21): 2518 - 2523.
[Abstract] [Full Text] [PDF]


Home page
Drug Metab. Dispos.Home page
F. C. Luft
Molecular Genetics of Salt-Sensitivity and Hypertension
Drug Metab. Dispos., April 1, 2001; 29(4): 500 - 504.
[Abstract] [Full Text]


Home page
HypertensionHome page
L. Raij
Workshop: Hypertension and Cardiovascular Risk Factors : Role of the Angiotensin II-Nitric Oxide Interaction
Hypertension, February 1, 2001; 37(2): 767 - 773.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
J. Jordan, H. R. Toka, K. Heusser, O. Toka, J. R. Shannon, J. Tank, A. Diedrich, C. Stabroth, M. Stoffels, R. Naraghi, et al.
Severely Impaired Baroreflex-Buffering in Patients With Monogenic Hypertension and Neurovascular Contact
Circulation, November 21, 2000; 102(21): 2611 - 2618.
[Abstract] [Full Text] [PDF]


Home page
Br J OphthalmolHome page
L.-O. Hattenbach, H. R Toka, O. Toka, H. Schuster, and F. C Luft
Absence of hypertensive retinopathy in a Turkish kindred with autosomal dominant hypertension and brachydactyly
Br J Ophthalmol, December 1, 1998; 82(12): 1363 - 1365.
[Abstract] [Full Text]


Home page
StrokeHome page
R. Naraghi, H. Schuster, H. R. Toka, S. Bahring, O. Toka, O. Oztekin, N. Bilginturan, H. Knoblauch, T. F. Wienker, A. Busjahn, et al.
Neurovascular Compression at the Ventrolateral Medulla in Autosomal Dominant Hypertension and Brachydactyly
Stroke, September 1, 1997; 28(9): 1749 - 1754.
[Abstract] [Full Text]