Effect of Ultrasound in the Treatment of Primary Nocturnal Enuresis

2000 ◽  
Vol 34 (6) ◽  
pp. 361-365 ◽  
Author(s):  
Alim Kosar ◽  
Selami Akkus ◽  
Serpil Savas ◽  
Ahmet Ozturk ◽  
T. Ahmet Serel1 ◽  
...  
2007 ◽  
Vol 177 (4S) ◽  
pp. 277-277
Author(s):  
Saladin H. Alloussi ◽  
Christoph Lang ◽  
Schahnaz Alloussi ◽  
Helmut Madersbacher ◽  
Gerd Miirtz ◽  
...  

2000 ◽  
Vol 89 (4) ◽  
pp. 475-481 ◽  
Author(s):  
EM Ornitz ◽  
AT Russell ◽  
P Gabikian ◽  
J‐G Gehricke ◽  
D Guthrie

2016 ◽  
Vol 8 (4) ◽  
Author(s):  
Ersan Arda ◽  
Basri Cakiroglu ◽  
David T. Thomas

2017 ◽  
Vol 13 (4) ◽  
pp. 498-506
Author(s):  
Anna Krakowska ◽  
◽  
Michał Maternik ◽  
Agnieszka Wosiak ◽  
Monika Miklaszewska ◽  
...  

2008 ◽  
Vol 40 (3) ◽  
pp. 583-586 ◽  
Author(s):  
Cuneyt Ozden ◽  
Ozdem Levent Ozdal ◽  
Binhan Kagan Aktas ◽  
Alper Ozelci ◽  
Serkan Altinova ◽  
...  

2020 ◽  
Vol 13 (2) ◽  
pp. e231977
Author(s):  
Margarida Cunha ◽  
Mafalda Matias ◽  
Inês Marques

Ehlers-Danlos syndrome (EDS), hypermobility type, is probably the most common EDS type, as well as the most common heritable connective tissue disorder. Bladder dysfunction is a rare clinical manifestation of EDS and manifests itself as primary nocturnal enuresis. We present a 10-year-old boy referred to the paediatrics nephrology consultation due to primary nocturnal enuresis and day time symptoms of urinary urgency. During the appointment, a tendency to joint hypermobility was noted. On evaluation the skin was hyperextensible and the Beighton score was positive. The genetic testing revealed a variant of the COL5A1 gene not yet described in the literature.


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