Peptic Ulcer Disease (PUD)

Peptic ulcers are breaks that extend through the mucosa, typically occurring in the stomach or in the duodenum. The two primary causes of peptic ulcers are infection with a bacteria known as Helicobacter pylori or the use of nonsteroidal anti-inflammatory medications such as aspirin, ibuprofen or naproxen.  Smoking has also been associated with increased risk of PUD. Stress and diet were initially thought to predispose to PUD, but now are recognized to be of little or no risk.

 

Hereditary Hemochromatosis

Hereditary hemochromatosis (HH) is by far the most common inherited cause of iron overload (1). Without diagnosis and therapeutic intervention, there is a risk that iron overload will occur resulting in tissue damage and potentially premature death. Less common forms of iron overload associated with mutations of transferrin receptor 2, (TFR2), hepcidin, hemojuvelin, and a sub-type of ferroportin (1) will not be discussed. 

 

Celiac Sprue

Celiac Sprue, also known as gluten-sensitive enteropathy or nontropical sprue is a disease primarily affecting the small bowel caused by a reaction to gluten, a protein found in wheat, barley and rye. Over the past several decades, it has become apparent that celiac sprue is often underdiagnosed due to minimal or no clinical symptoms. Studies suggest that celiac sprue is present in 1:250 to 1:500 persons in most countries (1,2). Celiac sprue is particularly common in populations from Northern Europe and Western Ireland.