Zobrazeno 1 - 10
of 581
pro vyhledávání: '"Currarino syndrome"'
Autor:
Scimone, Concetta1,2, Donato, Luigi1,2, Rinaldi, Carmela1, Sidoti, Antonina1,2 asidoti@unime.it, D'Angelo, Rosalia1
Publikováno v:
Journal of Digestive Diseases. Sep2016, Vol. 17 Issue 9, p628-632. 5p.
Autor:
Masatoshi Shoji1 pignite@me.com, Naomi Nojima2 nnojima@tch.toyama.toyama.jp, Akemi Yoshikawa2 yoshikawaak@tch.toyama.toyama.jp, Wataru Fukushima2 fukushimaw@tch.toyama.toyama.jp, Naotaka Kadoya3 nkadoya@tch.toyama.toyama.jp, Hisashi Hirosawa2 hhirosawa@tch.toyama.toyama.jp, Ryohei Izumi2 rizumi@tch.toyama.toyama.jp
Publikováno v:
Journal of Medical Case Reports. 2014, Vol. 8 Issue 1, p1-12. 12p.
Publikováno v:
Radiology Case Reports, Vol 17, Iss 9, Pp 2936-2939 (2022)
Currarino syndrome is an autosomal dominant hereditary disease defined as a triad of anorectal abnormality, sacral dysgenesis, and a presacral mass, primarily an anterior sacral meningocele. It is often seen in children and considered rare in adults.
Externí odkaz:
https://doaj.org/article/86a86b2b04364fa6b795d4e829394867
Autor:
Diletta Dell'Apa, Martina Fumeo, Antonella Volta, Marco Bernardini, Francesca Fidanzio, Valentina Buffagni, Matthias Christen, Vidhya Jagannathan, Tosso Leeb, Ezio Bianchi
Publikováno v:
Frontiers in Veterinary Science, Vol 10 (2023)
Two boxer dogs from the same litter were presented at 3 months of age for urinary and fecal incontinence. Both dogs had an abnormal tail consisting of a small stump, an atonic anal sphincter, and absent perineal reflex and sensation. Neurological eva
Externí odkaz:
https://doaj.org/article/cf63138658f34f8a93a7478be67ab110
Autor:
Rasha A. Al-Youzbaki, Emad Hazim Mahmoud, Zahraa A. Alsubaihawi, Mohammed A. Almeran, Saja A. Albanaa, Samer S. Hoz
Publikováno v:
Romanian Neurosurgery, Vol 37, Iss 1 (2023)
Introduction: Currarino Syndrome (CS) is a rare entity characterized by a triad of sacral agenesis, anorectal malformations, and pre-sacral masses. CS is typically diagnosed during the first decade of life. Case Description: We present a rare case
Externí odkaz:
https://doaj.org/article/c9b27ff94fe9475893ff0395ac0d946f
Autor:
Gobbi, Dalia1 daliahg@yahoo.com, Zanatta, Cinzia1, Zanarotti, Roberta2, Trincia, Elena3, Midrio, Paola1
Publikováno v:
Pediatrics International. Sep2021, Vol. 63 Issue 9, p1131-1133. 3p.
Publikováno v:
Annals of Pediatric Surgery, Vol 18, Iss 1, Pp 1-6 (2022)
Abstract Background While sacrococcygeal teratoma (SCT) is a tumor originating from the tip of the sacrum, presacral tumors are accompanied by Currarino syndrome (CS) and classified as the Altman’s type IV sacrococcygeal tumors. They are quite diff
Externí odkaz:
https://doaj.org/article/729b3fdb140b47819656606c9a8b67ac
Publikováno v:
Journal of Clinical Imaging Science. Jan-Mar2015, Vol. 5 Issue 1, p1-3. 3p.
Autor:
Aydoseli, A.1 (AUTHOR), Akcakaya, M. O.1 (AUTHOR) moakcakaya@gmail.com, Aras, Y.1 (AUTHOR), Dolas, I.1 (AUTHOR), Yanar, H.2 (AUTHOR), Sencer, A.1 (AUTHOR)
Publikováno v:
British Journal of Neurosurgery. Dec2013, Vol. 27 Issue 6, p833-835. 3p.
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