Families with autosomal dominant brachydactyly type E, short stature, and severe hypertension

Annals of Internal Medicine

Volumn 129, Issue 3, 1998, Pages 204-208

  Toka, Hakan R ^a   Bähring, Sylvia ^a   Chitayat, David ^b   Melby, James C ^c   Whitehead, Richard ^c   Jeschke, Eva ^a   Wienker, Thomas F ^a   Toka, Okan ^a   Schuster, Herbert ^a   Luft, Friedrich C ^a  

^a FRANZ VOLHARD CLINIC   (Germany)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c BOSTON MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL DOMINANT INHERITANCE; BRACHYDACTYLY; CHROMOSOME 12P; CHROMOSOME MAP; CHROMOSOME SEGREGATION; CLINICAL ARTICLE; FAMILY HISTORY; FEMALE; HAPLOTYPE; HUMAN; HYPERTENSION; MALE; MOLECULAR GENETICS; MULTIGENE FAMILY; PRIORITY JOURNAL; SHORT STATURE; STROKE;

EID: 7344251715     PISSN: 00034819     EISSN: None     Source Type: Journal    
DOI: 10.7326/0003-4819-129-3-199808010-00008     Document Type: Article

References (11)

1. Lifton RP. Molecular genetics of human blood pressure variation. Science. 1996;272:676-80.
2. Schuster H, Wienker TF, Bähring S, Bilginturan N, Toka HR, Neitzel H, et al. Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12. Nat Genet. 1996;4:98-100.
3. Schuster H, Wienker TF, Toka HR, Bähring S, Jeschke E, Toka O, et al. Autosomal dominant hypertension and brachydactyly in a Turkish kindred resembles essential hypertension. Hypertension. 1996;28:1085-92.
4. Chitayat D, Grix A, Balfe JW, Abramowicz JS, Garza J, Fong CT, et al. Brachydactyly-short stature-hypertension syndrome: report on two families. Am J Med Genet. 1997;73:279-85.
5. Riccardi VM, Holmes LB. Brachydactyly, type E: hereditary shortening of digits, metacarpals, metatarsals, and long bones. J Pediatr. 1974;84:251-3.
6. Naraghi R, Geiger H, Crnac J, Huk W, Fahlbusch R, Engels G, et al. Posterior fossa neurovascular anomalies in essential hypertension. Lancet. 1994;344:1466-70.
7. Morimoto S, Sasaki S, Miki S, Kawa T, Itoh H, Nakata T, et al. Neurovascular compression of the rostral ventrolateral medulla related to essential hypertension. Hypertension. 1997;30:77-82.
8. Naraghi R, Schuster H, Toka HR, Bähring S, Toka O, Öztekin Ö, et al. Posterior fossa compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly. Stroke. 1997;28:1749-54.
9. Schuster H, Toka O, Toka HR, Busjahn A, Öztekin Ö, Wienker TF, et al. A cross-over medication trial for autosomal-dominant hypertension with brachydactyly. Kidney Int. 1998;53:167-72.
10. Brickman AS, Stern N, Sowers JR. Hypertension in pseudohypoparathyroidism type I. Am J Med. 1988;85:785-92.
11. Wilkie TM, Gilbert DJ, Olsen AS, Chen XN, Amatruda TT, Korenberg JR, et al. Evolution of the mammalian G protein αsubunit multigene family Nat Genet. 1992;1:85-91.