Primary Hypertrophic Osteoarthropathy (PHO) and Changes in the Joints:Clinical, X-ray, Scintigraphic, Arteariographic and Histologic Examination of 19 Patients

1980 ◽  
Vol 9 (2) ◽  
pp. 89-96 ◽  
Author(s):  
Ivo Jajić ◽  
Marko Pećina ◽  
Bogdan Krstulović ◽  
Davorin Kovačević ◽  
Fadila Pavičić ◽  
...  

2020 ◽  
Vol 58 (5) ◽  
pp. 544-549
Author(s):  
E. L. Trisvetova

The article presents information about a rare hereditary disease – primary hypertrophic osteoarthropathy with autosomal dominant and autosomal recessive inheritance. Genetic heterogeneity is responsible for the clinical polymorphism of symptoms that appear in childhood and adolescence. Differential diagnosis should be carried out with secondary hypertrophic osteoarthropathy, which occurs in 90% of cases and is associated with malignant neoplasms, rheumatic diseases and other diseases. X-ray signs are of great importance to clarify the localization, extent and nature of bone lesions. There is no specific treatment for the disease.





2006 ◽  
Vol 73 (4) ◽  
pp. 477-479 ◽  
Author(s):  
Mohamed Younes ◽  
Mongi Touzi ◽  
Ismail Béjia ◽  
Saoussen Zrour-Hassen ◽  
Najeh Amara ◽  
...  


2008 ◽  
Vol 40 (7) ◽  
pp. 927-927
Author(s):  
Sandeep Uppal ◽  
Christine P Diggle ◽  
Ian M Carr ◽  
Colin W G Fishwick ◽  
Mushtaq Ahmed ◽  
...  


1993 ◽  
Vol 14 (3) ◽  
pp. 181-182 ◽  
Author(s):  
Manuel Mart�nez-Lav�n ◽  
Carlos Pineda ◽  
Carmen Navarro ◽  
Alfonso Buend�a ◽  
Carlos Zabal


Author(s):  
Markus Braun-Falco ◽  
Henry J. Mankin ◽  
Sharon L. Wenger ◽  
Markus Braun-Falco ◽  
Stephan DiSean Kendall ◽  
...  




1989 ◽  
Vol 48 (3) ◽  
pp. 240-246 ◽  
Author(s):  
M Matucci-Cerinic ◽  
S Cinti ◽  
M Morroni ◽  
T Lotti ◽  
G Nuzzaci ◽  
...  


2011 ◽  
Vol 20 (6) ◽  
pp. 531-533 ◽  
Author(s):  
Carsten Bergmann ◽  
Marion Wobser ◽  
Henner Morbach ◽  
Albrecht Falkenbach ◽  
Dietrich Wittenhagen ◽  
...  


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