Gastrointestinal, Pelvic & Liver Disease, (A – Z)
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Extrahepatic Bile Duct
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The extrahepatic bile duct plays a crucial role in our digestive system, but when problems arise, they can be quite troublesome. The bile duct is a tube that ...

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Polysplenia
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Polysplenia is a rare medical condition where a person has multiple small spleens instead of the usual single, large spleen. This condition can have various ...

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Asplenia
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Asplenia is a medical condition where a person's spleen is either missing or not functioning properly. The spleen plays a crucial role in our immune system and ...

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What Is Biliary Atresia
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Biliary atresia is a rare but serious liver condition that affects infants. In this article, we will provide simple, easy-to-understand explanations of biliary ...

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Trihydroxycholestanoic Acid CoA Oxidase Deficiency
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Trihydroxycholestanoic acid CoA oxidase deficiency, also known as THCCoA oxidase deficiency or trihydroxycholestanoic acid oxidation disorder, is a rare ...

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Cerebrotendinous Xanthomatosis
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Cerebrotendinous xanthomatosis, or CTX for short, is a rare genetic disorder that affects a person's ability to break down certain fats in their body. In this ...

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Sterol 27-Hydroxylase Deficiency (CTX)
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Sterol 27-hydroxylase deficiency, also known as Cerebrotendinous Xanthomatosis (CTX), is a rare genetic disorder that affects the body's ability to metabolize ...

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Delta 4-3-Oxosteroid 5-Beta-Reductase Deficiency
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Delta 4-3-oxosteroid 5-beta-reductase deficiency, also known as 5-ARD, is a rare genetic condition that affects the way the body processes hormones called ...

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Bile Acid CoA Ligase Deficiency
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Bile Acid CoA Ligase Deficiency is a rare genetic disorder that affects the way our bodies process bile acids. Bile acids are essential for digesting fats in ...

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Amino Acid N-Acyltransferase Deficiency
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Amino Acid N-Acyltransferase Deficiency is a rare genetic disorder that affects the body's ability to process certain amino acids. In this article, we will ...

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Alpha-Methylacyl-CoA Racemase (AMACR) Deficiency
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Alpha-Methylacyl-CoA Racemase (AMACR) deficiency is a rare genetic disorder that affects the way our bodies process certain fats. In this article, we will ...

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3-Beta-Hydroxy-Delta-5-C27-Steroid Oxidoreductase Deficiency
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3-beta-hydroxy-delta-5-C27-steroid oxidoreductase deficiency, also known as HSD3B7 deficiency, is a rare genetic condition that affects the way our bodies ...

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Bile Acid Synthesis Disorders
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Bile Acid Synthesis Disorders (BASDs) are rare genetic conditions that affect the production of bile acids in the liver. Bile acids play a crucial role in ...

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Gastrointestinal Hemorrhage
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Gastrointestinal Hemorrhage, often referred to as GI bleeding, is a medical condition that involves bleeding in the digestive system. This article aims to ...

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Intestinal Lymphangiectasia
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Intestinal lymphangiectasia is a rare digestive disorder that affects the lymphatic system in your intestines. The lymphatic system is responsible for ...

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Hepatolenticular Degeneration
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Hepatolenticular degeneration, also known as Wilson's disease, is a rare genetic disorder that affects the body's ability to handle copper properly. In this ...

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Xanthomatous Biliary Cirrhosis
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Xanthomatous biliary cirrhosis, often referred to as primary biliary cirrhosis (PBC), is a rare and chronic liver disease that primarily affects women. It's ...

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Obstructive Liver Disease
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Obstructive liver disease is a condition that affects the liver's ability to function properly due to blockages in the bile ducts. In this article, we will ...

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Type 1 Diabetes 
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Type 1 diabetes – Diabetes means your blood glucose, or blood sugar, levels are too high. With type 1 diabetes, your pancreas does not make insulin. ...

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Primary Biliary Cholangitis
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Primary Biliary Cholangitis is irritation and swelling (inflammation) of the bile ducts of the liver. This blocks the flow of bile, which damages the liver ...

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