Zobrazeno 1 - 10
of 180
pro vyhledávání: '"Gallbladder agenesis"'
Autor:
Nasser Malekpour Alamdari, Adel Zeinalpour, Barmak Gholizadeh, Maryam Abbasi, Faezeh Shams, Hamed Ebrahimibagha
Publikováno v:
Caspian Journal of Internal Medicine, Vol 14, Iss 4, Pp 751-754 (2023)
Background: Gallbladder agenesis is a biliary tract related congenital malformation with an incidence of 10–65 per 100,000 and associated with other congenital abnormalities. GA is usually asymptomatic, but sometimes patients become symptomatic. Th
Externí odkaz:
https://doaj.org/article/333ed0f7b2f14409a13e9975a079c612
Autor:
Abdullahi Ibrahim, Mutisya Cosmas, Ngugi Moses, Osiemo Deborah, Gumbe Ester, Kiptoon Dan, Hungu Eric, Dahir Mohamed, Ojuka Daniel
Publikováno v:
The Annals of African Surgery, Vol 20, Iss 2, Pp 74-79 (2023)
Gallbladder agenesis (GA) is an uncommon congenital anomaly with an incidence of 0.09%. Lack of awareness, coupled with vague clinical and radiological characteristics, has led to infrequent preoperative diagnosis. This is the case of a 42-year-old f
Externí odkaz:
https://doaj.org/article/649fab91adfa4328823cb5b769946e26
Akademický článek
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Autor:
Nourah Alruqaie, Majid Alfadhel
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 1, Iss 2, Pp 87-92 (2018)
Background: Mitchell-Riley Syndrome (OMIM # 615710) is a rare autosomal recessive disorder, characterized by a genetic mutation in the RFX6 gene. Clinically it is presented with triad of neonatal diabetes, gall bladder agenesis/hypoplasia and intesti
Externí odkaz:
https://doaj.org/article/19fab7a79a3642ce99d912033387e94f
Akademický článek
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Publikováno v:
The Pan African Medical Journal, Vol 37, Iss 259 (2020)
Gallbladder agenesis is a rare congenital malformation characterized by the absence of the gallbladder and cystic duct due to an anomaly in the embryonic development. It is commonly associated with other congenital abnormalities, and the isolated for
Externí odkaz:
https://doaj.org/article/a5ba8448a9b84b86b3d777e68553996c
Autor:
Yoshihiko Takano, Mirei Hoshino, Sakae Iriyama, Kyoko Takayanagi, Manabu Ishiro, Nobuhiro Kawakami, Takayuki Okamura
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-4 (2018)
Abstract Background Gallbladder agenesis is a rare congenital malformation. More than 50% of cases are isolated and asymptomatic. These asymptomatic patients are principally healthy and need no interventions. However, some patients develop symptoms,
Externí odkaz:
https://doaj.org/article/3afc74959391475c9254a37a5e5698fb
Publikováno v:
Middle East Journal of Digestive Diseases, Vol 10, Iss 2, Pp 109-113 (2018)
Gallbladder agenesis (GA) is a rare congenital anomaly. Only 50% of the cases with GA are symptomatic, presenting mostly in the 4th or 5th decade of life. The clinical presentation of GA and imaging findings are non-specific and often misinterpreted
Externí odkaz:
https://doaj.org/article/f0e3f16aa10d4d60bbd3fce39720a603
Autor:
Ibrahim, Abdullahi, Cosmas, Mutisya, Moses, Ngugi, Deborah, Osiemo, Ester, Gumbe, Dan, Kiptoon, Eric, Hungu, Mohamed, Dahir, Daniel, Ojuka
Publikováno v:
Annals of African Surgery; Vol. 20 No. 2 (2023); 74-79
Gallbladder agenesis (GA) is an uncommon congenital anomaly with an incidence of 0.09%. Lack of awareness, coupled with vague clinical and radiological characteristics, has led to infrequent preoperative diagnosis. This is the case of a 42-year-old f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=78975075580c::f6b7f9a762e8ff6121944aea28bf51d9
https://www.ajol.info/index.php/aas/article/view/249438
https://www.ajol.info/index.php/aas/article/view/249438
Autor:
Eugenio Tagliaferri, Heinrich Bergmann, Sebastian Hammans, Aziz Shiraz, Eckhard Stüber, Christoph Seidlmayer
Publikováno v:
Case Reports in Gastroenterology, Vol 10, Iss 3, Pp 819-825 (2017)
Isolated agenesis of the gallbladder is usually a rare asymptomatic anatomical variation, with an estimated incidence of 10–65 per 100,000. Females are more commonly affected (ratio 3: 1), with the disease typically presenting in the second or thir
Externí odkaz:
https://doaj.org/article/68c681bcb4bc4b8f915046cf2575e3bb