Zobrazeno 1 - 10
of 106
pro vyhledávání: '"caudal dysgenesis"'
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
Akademický článek
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Autor:
Dell'Apa, Diletta, Fumeo, Martina, Volta, Antonella, Bernardini, Marco, Fidanzio, Francesca, Buffagni, Valentina, Christen, Matthias, Jagannathan, Vidhya, Leeb, Tosso, Bianchi, Ezio
Publikováno v:
Dell'Apa, Diletta; Fumeo, Martina; Volta, Antonella; Bernardini, Marco; Fidanzio, Francesca; Buffagni, Valentina; Christen, Matthias; Jagannathan, Vidhya; Leeb, Tosso; Bianchi, Ezio (2023). Case report: Sacral agenesis in two boxer dogs: clinical presentation, diagnostic investigations, and outcome. Frontiers in veterinary science, 10, p. 1201484. Frontiers Media 10.3389/fvets.2023.1201484
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::dddfe9bc62fb0b7f65572551f9e5df3e
https://hdl.handle.net/11577/3486360
https://hdl.handle.net/11577/3486360
Autor:
Ranjit I. Kylat, Mohammad Bader
Publikováno v:
Children, Vol 7, Iss 11, p 211 (2020)
Caudal Regression Syndrome (CRS) or Caudal dysgenesis syndrome (CDS) is characterized by maldevelopment of the caudal half of the body with variable involvement of the gastrointestinal, genitourinary, skeletal, and nervous systems. CRS affects 1–3
Externí odkaz:
https://doaj.org/article/24db598732634ddbb1017a4980ea9df7
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 7, Pp PD19-PD20 (2017)
Caudal Regression Syndrome (CRS) is a rare disorder which consists of abnormalities in the lumbosacral spine, rectum, urinary system and lower limbs. These abnormalities also include orthopaedic deformities, such as hip dislocation, knee-flexion c
Externí odkaz:
https://doaj.org/article/609ce80499344e62b50d7d27c97e10f2
Publikováno v:
Journal of Diagnostic Medical Sonography. 37:207-212
Sirenomelia is a rare, lethal congenital malformation of the fetus, typically characterized by the fusion of lower limbs and additional malformations involving the lumbosacral spine and urogenital and gastrointestinal tracts. We report a case of sire
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26adfc0a9d5fb2b6ce555bfb191b5e2d
https://doi.org/10.1177/8756479320975441
https://doi.org/10.1177/8756479320975441
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Marianne Begorre, Daniel Cailliez, Claire Beneteau, Pierre Chenal, Thierry Frebourg, Guillaume Benoist, François Lecoquierre, Raphaele Mangione, Florence Petit, Nicolas Gruchy, Louise Devisme, Sophie Patrier, Juliette Coursimault, Fanny Pelluard, Hubert Journel, Bénédicte Gérard, Marion Gérard, Pascale Saugier-Veber, Valérie Layet, Alain Liquier, Corinne Jeanne, Mirjam M. de Jong, Nadia Tillouche, Anne Bazin, Gaël Nicolas, Conny M. A. van Ravenswaaij-Arts, Anne-Claire Brehin, Wilfrid Finck, Sophie Coutant, Sophie Degre, Christine Francannet, Madeleine Joubert, Hélène Laurichesse Delmas
Publikováno v:
Human Mutation
Human Mutation, 2020, 41 (5), pp.926-933. ⟨10.1002/humu.23998⟩
Human Mutation, 41(5), 926-933. Wiley
Human Mutation, Wiley, 2020, 41 (5), pp.926-933. ⟨10.1002/humu.23998⟩
Human Mutation, 2020, 41 (5), pp.926-933. ⟨10.1002/humu.23998⟩
Human Mutation, 41(5), 926-933. Wiley
Human Mutation, Wiley, 2020, 41 (5), pp.926-933. ⟨10.1002/humu.23998⟩
Full access; International audience; Sirenomelia is a rare severe malformation sequence of unknown cause characterized by fused legs and severe visceral abnormalities. We present a series of nine families including two rare familial aggregations of s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4f4809cccfe22a8f8d876db3d7e0573
https://hdl.handle.net/11370/0ac3ca3a-6458-40da-92ae-b9d82ef21217
https://hdl.handle.net/11370/0ac3ca3a-6458-40da-92ae-b9d82ef21217