Prolonged Jaundice: Does urine sampling identify UTI’s or is it a waste of time?

Author(s):  
Emma WOOLLEY

The accessible lab diagnostic and expansion of knowledge about the important role of hormones in health regulation lead to the increase of the quantity of lab hormonal tests. Often patients prescribe diagnostic by themselves. Incorrect blood, salvia and urine sampling results in the incorrect diagnostic and treatment. The following article is focused on the rules of sampling for hormonal diagnostic.


Author(s):  
Gianluigi Ardissino ◽  
Antonio Vergori ◽  
Cesare Vergori ◽  
Laura Martelli ◽  
Valeria Daccò ◽  
...  

Author(s):  
Fiorella Lucarini ◽  
Marc Blanchard ◽  
Tropoja Krasniqi ◽  
Nicolas Duda ◽  
Gaëlle Bailat Rosset ◽  
...  

Carrying out exposure studies on children who are not toilet trained is challenging because of the difficulty of urine sampling. In this study, we optimized a protocol for urine collection from disposable diapers for the analysis of phthalate metabolites. The exposure of Swiss children (n = 113) between 6 months and 3 years of life to seven phthalates was assessed by gas chromatography–mass spectrometry measurements. The study showed limited exposures to phthalates, with only 22% of the samples containing some of the metabolites investigated. The three most frequently detected metabolites were monoethyl phthalate, mono-cyclohexyl phthalate, and mono-benzyl phthalate. We also detected mono-n-octyl phthalate and mono(3,5,5-trimethylhexyl) phthalate, which have rarely been observed in urine from infants and toddlers; therefore, di-n-octyl phthalate and bis(3,5,5-trimethylhexyl) phthalate can be considered as potentially new emerging phthalates. This study presents an initial snapshot of the Swiss children’s exposure to phthalates and provides a promising approach for further phthalate biomonitoring studies on young children using disposable diapers as urine sampling technique.


2017 ◽  
Vol 381 ◽  
pp. 193-194
Author(s):  
A. Karimova ◽  
G. Mukhambetova ◽  
A. Izbassarova ◽  
G. Kadrzhanova ◽  
N. Bozhbanbayeva ◽  
...  

Author(s):  
Tamar R. Lubell ◽  
Jonathan Barasch ◽  
Paul King ◽  
Julie Ochs ◽  
Manasi Chitre ◽  
...  

1985 ◽  
Vol 15 (1) ◽  
pp. 18-22 ◽  
Author(s):  
Masayuki Yamamoto ◽  
Hideki Fujii ◽  
Katsuhiko Sugahara ◽  
Sadao Kawashima ◽  
Kazue Ozawa ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-5 ◽  
Author(s):  
Tamer Rizk ◽  
Adel Mahmoud ◽  
Tahani Jamali ◽  
Salah Al-Mubarak

Aim. We aim to describe a female patient with Menkes disease who presented with epilepsia partialis continua.Case Presentation. Seventeen-months-old Saudi infant was presented with repetitive seizures and was diagnosed to have epilepsia partialis continua.Discussion. Menkes disease (OMIM: 309400) is considered a rare, X-linked recessive neurodegenerative disorder resulting from a mutation in the gene coding for the copper transporting ATPase (ATP7A). Affected individuals usually present with kinky hair, skeletal changes, prolonged jaundice, hypothermia, developmental regression, decreased tone, spasticity, weakness, and therapy resistant seizures.Conclusion. Raising awareness of abnormal presentation of this rare disease may help in the control of seizures through subcutaneous copper supplementation.


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