Turner syndrome is a rare condition in women that is associated with either complete or
partial loss of one X chromosome, often in mosaic karyotypes. Turner syndrome is …

It is well established that portal hypertension can occur in the absence of cirrhosis, as
reported in patients with immune disorders, infections and thrombophilia. However, similar …

Fatty liver accumulation results from an imbalance between lipid deposition and removal,
driven by the hepatic synthesis of triglycerides and de novo lipogenesis. The habitual diet …

Iron deficiency anemia (IDA) is associated with a number of pathological gastrointestinal
conditions other than inflammatory bowel disease, and also with liver disorders. Different …

Idiopathic non-cirrhotic portal hypertension (INCPH) is a clinicopathologic disease entity
characterized by the presence of clinical signs and symptoms of portal hypertension (PH) in …

Idiopathic non‐cirrhotic portal hypertension (INCPH) is a rare vascular liver disease that has
attracted new interest in recent years. It is characterised by clinical signs of portal …

Common variable immunodeficiency (CVID) is a primary B-cell immunodeficiency disorder,
characterized by remarkable hypogammaglobulinemia. The disease can develop at any age …

Background The knowledge of natural history of patients with portal hypertension (PH) not
due to cirrhosis is less well known than that of cirrhotic patients. Aim To describe the clinical …

Wilson disease (WD) is an autosomal recessive disorder that is caused by the toxic
accumulation of copper (Cu) in the liver. The ATP7B gene, which is mutated in WD, encodes …

Common variable immunodeficiency (CVID) is one of the inborn errors of immunity that have
the greatest clinical impact. Rates of morbidity and mortality are higher in patients with CVID …