Results 21 to 30 of about 23,080 (290)

Late presentation of incomplete jejunal atresia

Journal of Pediatric Surgery Case Reports, 2020
Intestinal atresia is a life-threatening cause of intestinal obstruction in the neonate, and rarely a cause of intestinal obstruction in an infant. We report a rare presentation of an incomplete jejunal atresia in a 1-year and 7 months old girl.
Elroy P. Weledji, Naiza Monono, Theophil Nana   +2 more
doaj   +1 more source

Intestinal Atresia in Finland: Maternal Risk Factors, Prevalence, Associated Anomalies and Survival. [PDF]

Acta Paediatr
ABSTRACT Aim We aimed to investigate prevalence, associated anomalies and survival of congenital intestinal atresia and to examine maternal risk factors for jejunoileal atresia (JIA). Methods All children born with, or pregnancies terminated because of, JIA or colonic atresia (CA) in Finland during 1987–2019 were identified from the Finnish Register of
Tahkola E, Raitio A, Helenius I, Syvänen J, Kemppainen T, Löyttyniemi E, Leinonen MK, Gissler M, Luoto T, Pakarinen MP.   +9 more
europepmc   +2 more sources

Changes of smooth muscle contractile filaments in small bowel atresia [PDF]

, 2012
AIM: To investigate morphological changes of intestinal smooth muscle contractile fibres in small bowel atresia patients. METHODS: Resected small bowel specimens from small bowel atresia patients (n = 12) were divided into three sections (proximal ...
Fiegel, Henning C., Gfrörer, Stefan, Metzger, Roman, Ramachandran, Priya, Rolle, Udo   +4 more
core   +1 more source

Monozygotic twins with jejuno-ileal atresia

Journal of Pediatric Surgery Case Reports, 2019
Introduction: Intestinal atresia is a congenital anomaly of the alimentary canal characterised by discontinuity of the bowel lumen that leads to intestinal obstruction in neonates.
Dennis Mazingi, Tungamirai Gwatirisa, Bothwell A. Mbuwayesango, Taurai Zimunhu, Shamiso Chowe, Kudzayi Munanzvi, Precious Mutambanengwe, Constantine Muparadzi, Mugove Moyo   +8 more
doaj   +1 more source

Live transplantation in children with biliary atresia and vascular anomalies [PDF]

, 1974
Eight of 29 infants and children undergoing orthotopic liver transplantation for extrahepatic biliary atresia had associated major vascular anomalies.
Lilly, JR, Starzl, TE
core   +1 more source

Intestinal transplantation in children under FK 506 immunosuppression [PDF]

, 1993
Intestinal transplantation, solitary (n = 3) or in combination with the liver (n = 7), was performed in 10 pediatric patients with intestinal failure. The liver was only replaced if there was liver failure and portal hypertension.
Adrian Casavilla, Andreas G. Tzakis, Anthony J. Demetris, Bakr Nour, David H. Van Thiel, Eduardo Yunis, Goulet, Grant, Iwaki, Jorge Reyes, Kareem Abu-Elmagd, Murase, Murase, Rick Selby, Samuel Kocoshis, Satoru Todo, Schraut, Shaffer, Starzl, Starzl, Starzl, Thomas E. Starzl, Todo, Todo, Tzakis, Tzakis, Zhong   +26 more
core   +1 more source

Intestinal Atresia

Clinics in Perinatology, 1978
Forty-five patients with intestinal atresia, including 20 with duodenal, 21 with jejunoileal, and 3 with colonic obstruction, were encountered at the Yale-New Haven Hospital between 1970 and 1976. The overall survival rate in the 43 operated cases was 93 per cent.
J A, Olvera Durán, R, Peniche García
openaire   +4 more sources

Liver transplantation before 1 year of age [PDF]

, 1987
Since 1981, 20 infants younger than 1 year of age received 26 orthotopic liver transplants. Immunosuppression was with cyclosporine and corticosteroids. Thirteen (65%) of the reciplents were discharged from the hospital.
Ascher, Baburao Koneru, Carlos O. Esquivel, Frederick Karrer, Gartner, Gordon, Iwatsuki, Kasai, Leonard Makowka, Robert D. Gordon, Rosenthal, Satoru Todo, Shunzaburo Iwatsuki, Starzl, Starzl, Starzl, Starzl, Thomas E. Starzl, Wallis J. Marsh   +18 more
core   +1 more source

Waitlist mortality of young patients with biliary atresia: Impact of allocation policy and living donor liver transplantation

Liver Transplantation, EarlyView., 2022
Abstract Patients with biliary atresia (BA) below 2 years of age in need of a transplantation largely rely on partial grafts from deceased donors (deceased donor liver transplantation [DDLT]) or living donors (living donor liver transplantation [LDLT]).
Hedayatullah Esmati, Marieke van Rosmalen, Patrick F. van Rheenen, Marieke T. de Boer, Aad P. van den Berg, Hubert P. J. van der Doef, Michel Rayar, Ruben H.J. de Kleine, Robert J. Porte, Vincent E. de Meijer, Henkjan J. Verkade   +10 more
wiley   +1 more source

Staged surgical treatment of apple peel intestinal atresia

Journal of Pediatric Surgery Case Reports, 2019
Apple peel atresia is an uncommon cause of intestinal obstruction. The authors report a case of a 36 weeks preterm girl, presenting with a fetal intestinal obstruction on prenatal ultrasonography, that was intraoperatively diagnosed with small bowel ...
Jalles Filipa, Morgado Mariana, Janeiro Marta, Gonçalves Miroslava   +3 more
doaj   +1 more source