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The clinical presentation of intestinal lymphangiectasia can range from asymptomatic to severe, implying a broad clinical spectrum. [4] Some patients may exhibit minimal or subtle clinical features, diverging from the "textbook" presentations often associated with severe cases in adults. [4]
Waldmann's disease, Primary intestinal lymphangiectasia Waldmann disease, also known as Primary Intestinal Lymphangiectasia (PIL), is a rare disease [ 1 ] characterized by enlargement of the lymph vessels supplying the lamina propria of the small intestine . [ 2 ]
Hennekam syndrome, also known as intestinal lymphagiectasia–lymphedema–mental retardation syndrome, [1] is an autosomal recessive disorder consisting of intestinal lymphangiectasia, facial anomalies, peripheral lymphedema, and mild to moderate levels of growth and intellectual disability.
Aplasia cutis congenita-intestinal lymphangiectasia syndrome is a very rare genetic disorder which is characterized by aplasia cutis congenita, intestinal lymphangiectasia-induced generalized edema, hypoproteinemia, and lymphopenia. [1] [2] It has been described in two Ashkenazi Jewish brothers. [3] [4]
Intestinal infections, such as gastroenteritis, can cause localized pain, often accompanied by nausea, vomiting, or diarrhea. Gastroenteritis, often called the “ stomach flu ,” is an infection ...
The signs and symptoms of protein losing enteropathy include diarrhea, fever, and general abdominal discomfort. [4] Swelling of the legs due to peripheral edema can also occur; however, if the PLE is related to a systemic disease such as congestive heart failure or constrictive pericarditis, then these symptoms could be due directly to the underlying illness. [2]
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Aplasia cutis congenita intestinal lymphangiectasia; Aplasia cutis congenita of limbs recessive; Aplasia cutis congenita recessive; Aplasia cutis-myopia; Aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits and nails; Aplastic anemia; Aplastic crisis; Apo A-I deficiency; Apolipoprotein C-II deficiency; Apparent ...