نتایج جستجو برای: ductal plate malformation

تعداد نتایج: 106447  

2018
K Sato M Sakai S Hayakawa Y Sakamoto Y Kagawa K Kutara K Teshima K Asano T Watari

BACKGROUND Gallbladder agenesis (GBA) is extremely rare in dogs. HYPOTHESIS/OBJECTIVES To describe the history, clinical signs, diagnosis, treatment, and outcomes of dogs with GBA. ANIMALS Seventeen client-owned dogs with GBA. METHODS Medical records from 2006 through 2016 were retrospectively reviewed. Dogs were included when GBA was suspected on abdominal ultrasonography and confirmed b...

Journal: :Journal of clinical and experimental hepatology 2023

Background And Aim: Biliary atresia (BA) can be associated with ductal plate malformation (DPM) like changes in as high 40% of patients. It is variable prognosis, most the studies suggesting poor overall outcome. Aim isto study clinical and histological parameters biliary patients without DPM. Methods: Medical records diagnosed from January 2021 to September 2022 were analyzed. Histology every ...

2017
Kamil Janowski Maria Goliszek Joanna Cielecka-Kuszyk Irena Jankowska Joanna Pawłowska

Congenital hepatic fibrosis (CHF) is a rare, autosomal recessive disorder, clinically characterized by hepatic fibrosis and portal hypertension. CHF results from ductal plate malformation (DPM) of the intrahepatic bile ducts. Four clinical forms can be observed: portal hypertensive, cholangitic, mixed and latent. CHF is one of the "fibropolycystic diseases" which also include several conditions...

Journal: :Indian Journal of Radiology and Imaging 2017

Journal: :Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2006
L F Menezes L F Onuchic

Autosomal recessive polycystic kidney disease (ARPKD) is an inherited disease characterized by a malformation complex which includes cystically dilated tubules in the kidneys and ductal plate malformation in the liver. The disorder is observed primarily in infancy and childhood, being responsible for significant pediatric morbidity and mortality. All typical forms of ARPKD are caused by mutatio...

Journal: :Human mutation 2009
Francesco Brancati Miriam Iannicelli Lorena Travaglini Annalisa Mazzotta Enrico Bertini Eugen Boltshauser Stefano D'Arrigo Francesco Emma Elisa Fazzi Romina Gallizzi Mattia Gentile Damir Loncarevic Vlatka Mejaski-Bosnjak Chiara Pantaleoni Luciana Rigoli Carmelo D Salpietro Sabrina Signorini Gilda Rita Stringini Alain Verloes Dominika Zabloka Bruno Dallapiccola Joseph G Gleeson Enza Maria Valente

The acronym COACH defines an autosomal recessive condition of Cerebellar vermis hypo/aplasia, Oligophrenia, congenital Ataxia, Coloboma and Hepatic fibrosis. Patients present the "molar tooth sign", a midbrain-hindbrain malformation pathognomonic for Joubert Syndrome (JS) and Related Disorders (JSRDs). The main feature of COACH is congenital hepatic fibrosis (CHF), resulting from malformation o...

Journal: :BMJ case reports 2015
Alexander Schlachterman Jonathan Hussain Roberto Firpi

To cite: Schlachterman A, Hussain J, Firpi R. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2015211141 DESCRIPTION A 45-year-old Caucasian woman, with no known liver disease, was referred to hepatology clinic for liver biopsy after abnormal image findings during a recent adult chicken pox infection. She presented with mildly elevated alkaline phosphatase of 170 ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید