Long-Term Follow-Up of GH-Treated Girls with Turner Syndrome: BMI, Blood Pressure, Body Proportions

2009 ◽  
Vol 71 (6) ◽  
pp. 336-342 ◽  
Author(s):  
Ellen M.N. Bannink ◽  
Roel L.F. van der Palen ◽  
Paul G.H. Mulder ◽  
Sabine M.P.F. de Muinck Keizer-Schrama
2008 ◽  
Vol 40 (1) ◽  
pp. 1-5 ◽  
Author(s):  
Lothar Pelz ◽  
Hellgard Köbschall ◽  
Ulla-Grit Lübcke ◽  
Gabriele Krüger ◽  
Georg-Klaus Hinkel ◽  
...  

1992 ◽  
Vol 6 (3) ◽  
pp. 195-197 ◽  
Author(s):  
G. ZANETTI ◽  
E. MONTANARI ◽  
A. TRINCHIERI ◽  
A. GUARNERI ◽  
A. CERESOLI ◽  
...  

2019 ◽  
Vol 26 (12) ◽  
pp. 1479-1486 ◽  
Author(s):  
J. Gregson ◽  
N. Qizilbash ◽  
M. Iwagami ◽  
I. Douglas ◽  
M. Johnson ◽  
...  

2020 ◽  
Vol 30 (12) ◽  
pp. 1976-1977
Author(s):  
Abraham Groner ◽  
Asad Qadir

AbstractPatients with a known genetic cause of aortic root dilation usually have a single underlying aetiology, either a single gene defect as in Marfan syndrome or chromosomal anomaly as in Turner syndrome. However, it is possible, although unlikely, for a patient to inherit multiple independent risk factors for aortic root dilation. We describe such a patient, who inherited Marfan syndrome and a very unusual form of mosaic Turner syndrome. Long-term follow-up of this patient may provide insight into the natural history of this unique genetic combination.


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