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10.1177/0883073815592222 http://scihub22266oqcxt.onion/10.1177/0883073815592222 C4990005!4990005!26184484     free     free     free Deprecated: Implicit conversion from float 235.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 235.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 235.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 235.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Child+Neurol 2016 ; 31 (3): 309-20 Nephropedia Template TP {{tp|p=26184484|t=2016. 236 children with developmental hydrocephalus: causes and clinical consequences |pdf=|usr=}}{{26184484}} gab.com Text 236 children with developmental hydrocephalus: causes and clinical consequences JO: J Child Neurol http://www.kidney.de/pget.php?&tw=1&pmid=26184484 #FOAvip Few systematic assessments of developmental forms of hydrocephalus exist. We reviewed MRIs and clinical records of patients with infancy-onset hydrocephalus. Among 411 infants, 236 had hydrocephalus with no recognizable extrinsic cause. These children were assigned to one of five subtypes and compared on the basis of clinical characteristics, developmental and surgical outcomes. At an average age of 5.3 years, 72% of children were walking independently and 87% could eat by mouth. 18% had epilepsy. Distinct patterns of associated malformations and syndromes were observed within each subtype. On average, children with aqueductal obstruction, cysts and encephaloceles had worse clinical outcomes than those with other forms of developmental hydrocephalus. 53% of surgically-treated patients experienced at least one shunt failure, but hydrocephalus associated with posterior fossa crowding required fewer shunt revisions. We conclude that each subtype of developmental hydrocephalus is associated with distinct clinical characteristics, syndromology, and outcomes, suggesting differences in underlying mechanisms. Twit Text FOAVip 236 children with developmental hydrocephalus: causes and clinical consequences ????J Child Neurol http://www.kidney.de/pget.php?&tw=1&pmid=26184484 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26184484 #FOAvip English Wikipedia <ref>{{Cite pmid|26184484}}</ref> 236 children with developmental hydrocephalus: causes and clinical consequences #MMPMID26184484 Tully HM; Ishak GE; Rue TC; Dempsey JC; Browd SR; Millen KJ; Doherty D; Dobyns WB J Child Neurol 2016[Mar]; 31 (3): 309-20 PMID26184484show ga Few systematic assessments of developmental forms of hydrocephalus exist. We reviewed MRIs and clinical records of patients with infancy-onset hydrocephalus. Among 411 infants, 236 had hydrocephalus with no recognizable extrinsic cause. These children were assigned to one of five subtypes and compared on the basis of clinical characteristics, developmental and surgical outcomes. At an average age of 5.3 years, 72% of children were walking independently and 87% could eat by mouth. 18% had epilepsy. Distinct patterns of associated malformations and syndromes were observed within each subtype. On average, children with aqueductal obstruction, cysts and encephaloceles had worse clinical outcomes than those with other forms of developmental hydrocephalus. 53% of surgically-treated patients experienced at least one shunt failure, but hydrocephalus associated with posterior fossa crowding required fewer shunt revisions. We conclude that each subtype of developmental hydrocephalus is associated with distinct clinical characteristics, syndromology, and outcomes, suggesting differences in underlying mechanisms. ä236 children with developmental hydrocephalus: causes and clinical con(epmc).pdf DeepDyve Pubget Overpricing