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10.1007/8904_2016_18 http://scihub22266oqcxt.onion/10.1007/8904_2016_18 C5585107!5585107!27858370     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27858370&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       JIMD+Rep 2017 ; 35 (ä): 17-22 Nephropedia Template TP {{tp|p=27858370|t=2017. Intracranial Hypertension in Cystinosis Is a Challenge: Experience in a Children?s Hospital |pdf=|usr=}}{{27858370}} gab.com Text Intracranial Hypertension in Cystinosis Is a Challenge: Experience in a Children s Hospital JO: JIMD Rep http://www.kidney.de/pget.php?&tw=1&pmid=27858370 #FOAvip Background: Cystinosis is a rare systemic lysosomal disease affecting mainly the kidney and eye. Ocular involvement in cystinosis is universal being the presence of cystine crystals in the cornea a diagnostic criterion and one of the earliest manifestations of the disease. Neuro-ophthalmologic manifestations are considered a rare and late complication in these patients. The aim of this article is to report the unexpectedly high incidence of intracranial hypertension in children with cystinosis at our centre.Methods: This study included eight children (0?16 years of age) with cystinosis seen at the paediatric ophthalmology department, Hospital Universitari Vall d?Hebron (Barcelona, Spain), a tertiary hospital, over the last 5 years.Results: Three girls and five boys, mean age: 9.6 years (range: 5?14 years), were studied. During follow-up, 4 out of 8 developed papilledema and confirmed high cerebrospinal fluid (CSF) pressure. The only symptomatic child presented an Arnold?Chiari anomaly with enlarged ventricles, whereas the other three, all asymptomatic, were diagnosed by scheduled fundoscopy and had normal neuroimaging studies. All four patients had at least one known risk factor for developing intracranial hypertension: initiation of growth hormone therapy, tapering of corticosteroids, acute renal failure and Arnold?Chiari malformation. Two of them required a ventriculoperitoneal shunt.Conclusions: Our results show that intracranial hypertension can occur more frequently than expected in patients with cystinosis. Furthermore, visual prognosis depends on early diagnosis and prompt treatment. A multidisciplinary approach is necessary, and we recommend fundoscopic examinations in all paediatric patients with cystinosis whether or not they present symptoms. Twit Text FOAVip Intracranial Hypertension in Cystinosis Is a Challenge: Experience in a Children s Hospital ????JIMD Rep http://www.kidney.de/pget.php?&tw=1&pmid=27858370 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27858370 #FOAvip English Wikipedia <ref>{{Cite pmid|27858370}}</ref> Intracranial Hypertension in Cystinosis Is a Challenge: Experience in a Children?s Hospital #MMPMID27858370 Martín-Begué N; Alarcón S; Wolley-Dod C; Lara LE; Madrid Á; Cano P; del Toro M; Ariceta G; Baumgartner MR; Patterson M; Rahman S; Peters V; Morava E; Zschocke J JIMD Rep 2017[]; 35 (ä): 17-22 PMID27858370show ga Background: Cystinosis is a rare systemic lysosomal disease affecting mainly the kidney and eye. Ocular involvement in cystinosis is universal being the presence of cystine crystals in the cornea a diagnostic criterion and one of the earliest manifestations of the disease. Neuro-ophthalmologic manifestations are considered a rare and late complication in these patients. The aim of this article is to report the unexpectedly high incidence of intracranial hypertension in children with cystinosis at our centre.Methods: This study included eight children (0?16 years of age) with cystinosis seen at the paediatric ophthalmology department, Hospital Universitari Vall d?Hebron (Barcelona, Spain), a tertiary hospital, over the last 5 years.Results: Three girls and five boys, mean age: 9.6 years (range: 5?14 years), were studied. During follow-up, 4 out of 8 developed papilledema and confirmed high cerebrospinal fluid (CSF) pressure. The only symptomatic child presented an Arnold?Chiari anomaly with enlarged ventricles, whereas the other three, all asymptomatic, were diagnosed by scheduled fundoscopy and had normal neuroimaging studies. All four patients had at least one known risk factor for developing intracranial hypertension: initiation of growth hormone therapy, tapering of corticosteroids, acute renal failure and Arnold?Chiari malformation. Two of them required a ventriculoperitoneal shunt.Conclusions: Our results show that intracranial hypertension can occur more frequently than expected in patients with cystinosis. Furthermore, visual prognosis depends on early diagnosis and prompt treatment. A multidisciplinary approach is necessary, and we recommend fundoscopic examinations in all paediatric patients with cystinosis whether or not they present symptoms. äIntracranial Hypertension in Cystinosis Is a Challenge: Experience in (epmc).pdf DeepDyve Pubget Overpricing