questionsmedicales.fr
Système digestif
Système digestif : Questions médicales fréquentes
Termes MeSH sélectionnés :
Multifactorial Inheritance
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└─
Voies biliaires
Biliary Tract
D001659
-
A03.159
└─
Tube digestif
Gastrointestinal Tract
D041981
-
A03.556
└─
Foie
Liver
D008099
-
A03.620
└─
Pancréas
Pancreas
D010179
-
A03.734
└─└─
Conduits biliaires
Bile Ducts
D001652
-
A03.159.183
└─└─
Vésicule biliaire
Gallbladder
D005704
-
A03.159.439
└─└─
Intestins
Intestines
D007422
-
A03.556.124
└─└─
Tube digestif inférieur
Lower Gastrointestinal Tract
D041741
-
A03.556.249
└─└─
Tube digestif supérieur
Upper Gastrointestinal Tract
D041742
-
A03.556.875
└─└─
Conduits biliaires intrahépatiques
Bile Ducts, Intrahepatic
D001653
-
A03.620.150
└─└─
Conduits pancréatiques
Pancreatic Ducts
D010183
-
A03.734.667
└─└─└─
Conduits biliaires extrahépatiques
Bile Ducts, Extrahepatic
D017734
-
A03.159.183.079
└─└─└─
Intestin grêle
Intestine, Small
D007421
-
A03.556.124.684
└─└─└─
Iléum
Ileum
D007082
-
A03.556.249.124
└─└─└─
Gros intestin
Intestine, Large
D007420
-
A03.556.249.249
└─└─└─
Jéjunum
Jejunum
D007583
-
A03.556.249.750
└─└─└─
Duodénum
Duodenum
D004386
-
A03.556.875.249
└─└─└─
Oesophage
Esophagus
D004947
-
A03.556.875.500
└─└─└─
Estomac
Stomach
D013270
-
A03.556.875.875
└─└─└─
Canalicules biliaires
Bile Canaliculi
D001648
-
A03.620.150.125
└─└─└─
Ampoule hépatopancréatique
Ampulla of Vater
D014670
-
A03.734.667.500
└─└─└─└─
Conduit cholédoque
Common Bile Duct
D003135
-
A03.159.183.079.300
└─└─└─└─
Conduit cystique
Cystic Duct
D003549
-
A03.159.183.079.450
└─└─└─└─
Conduit hépatique commun
Hepatic Duct, Common
D006500
-
A03.159.183.079.600
└─└─└─└─
Valvule iléocaecale
Ileocecal Valve
D007080
-
A03.556.249.124.400
└─└─└─└─
Canal anal
Anal Canal
D001003
-
A03.556.249.249.070
└─└─└─└─
Caecum
Cecum
D002432
-
A03.556.249.249.209
└─└─└─└─
Côlon
Colon
D003106
-
A03.556.249.249.356
└─└─└─└─
Rectum
Rectum
D012007
-
A03.556.249.249.767
└─└─└─└─
Glandes duodénales
Brunner Glands
D002011
-
A03.556.875.249.322
└─└─└─└─
Cardia
Cardia
D002299
-
A03.556.875.875.163
└─└─└─└─
Jonction oesogastrique
Esophagogastric Junction
D004943
-
A03.556.875.875.330
└─└─└─└─
Fundus gastrique
Gastric Fundus
D005748
-
A03.556.875.875.419
└─└─└─└─
Moignon gastrique
Gastric Stump
D018530
-
A03.556.875.875.578
└─└─└─└─
Antre pylorique
Pyloric Antrum
D011706
-
A03.556.875.875.716
└─└─└─└─
Pylore
Pylorus
D011708
-
A03.556.875.875.799
└─└─└─└─└─
Appendice vermiforme
Appendix
D001065
-
A03.556.249.249.209.290
└─└─└─└─└─
Côlon ascendant
Colon, Ascending
D044682
-
A03.556.249.249.356.333
└─└─└─└─└─
Côlon descendant
Colon, Descending
D044683
-
A03.556.249.249.356.500
└─└─└─└─└─
Côlon sigmoïde
Colon, Sigmoid
D012809
-
A03.556.249.249.356.668
└─└─└─└─└─
Côlon transverse
Colon, Transverse
D044684
-
A03.556.249.249.356.834
└─└─└─└─└─
Muscle sphincter de l'ampoule hépatopancréatique
Sphincter of Oddi
D009803
-
A03.556.875.249.160.572
└─└─└─└─└─
Sphincter inférieur de l'oesophage
Esophageal Sphincter, Lower
D049630
-
A03.556.875.875.330.350
In hemophilia and von Willebrand disease, the degree of alteration of laboratory assays correlates with bleeding manifestations. Few studies have assessed the predictive value for bleeding of laborato...
To assess whether there is an association between platelet function assay results and bleeding history, as evaluated by the International Society on Thrombosis and Haemostasis (ISTH) bleeding assessme...
Centers participating in the international ISTH-BAT validation study were asked to provide results of the diagnostic assays employed for the patients they enrolled, and the association with the indivi...
Sixty-eight patients with 14 different IPFDs were included. Maximal amplitude of platelet aggregation was significantly lower in patients with a pathologic BS and correlated inversely with the BS, a f...
This study shows that altered platelet laboratory assay results are associated with an abnormal ISTH-BAT BS in IPFD....
We report here an instructive case referred at 16 months-old for exploration of hemolysis without anemia (compensated anemia with reticulocytosis). The biology tests confirmed the hemolysis with incre...
The major genetic group of Toxoplasma gondii, known as type I, generally displays high lethality in laboratory Mus musculus (mouse) strains, with few exceptions. However, because rodents are the prima...
The ELMOD3 gene is implicated in causing autosomal recessive/dominant non-syndromic hearing loss in humans. However, the etiology has yet to be completely elucidated. In this study, we generated a pat...
The mucopolysaccharidoses (MPS), Pompe Disease (PD), and Krabbe disease (KD) are inherited conditions known as lysosomal storage disorders (LSDs) The resulting enzyme deficiencies give rise to progres...
Inherited retinal diseases (IRD) are a leading cause of blindness in the working age population and children. The scope of this review is to familiarise clinicians and scientists with the current land...
The present review aims to summarize the state-of-the-art von Willebrand disease (VWD) treatment focusing on specific clinical settings (obstetrics, surgery, long-term prophylaxis and comorbidities) a...
Literature research and case reports....
Considering that patients affected by VWD have an intact ability to synthesize FVIII, in order to avoid excessive levels of FVIII, a highly purified plasma VWF concentrate with low FVIII content could...
Human-derived experimental systems such as induced pluripotent stem cell (iPSC)-derived models are useful tools to study mechanisms and potential therapeutic approaches for mitochondrial disorders. He...
The ITM2B-related retinal dystrophy (ITM2B-RD) was identified within patients carrying the autosomal dominant variant [c.782A > C, p.(Glu261Ala)] in ITM2B from whom induced pluripotent stem cell (IPSC...