Ménétrier’s disease with normal albumin level
نویسندگان
چکیده
منابع مشابه
A Case of Bruton’s Disease with Normal Immunoglobulin G Level
X-linked agamaglobulinemia (XLA) or Bruton’s disease is a genetic disease resulting from a mutation in the Bruton’s tyrosine kinase (Btk) gene. This mutation leads to B cell arrest during differentiation (1). This disease was first described by Ogden Bruton in 1952 (2). Approximately 85% of the affected subjects are male (3). This disorder is inherited as an X-linked recessive trait. Carrier fe...
متن کاملa case of bruton’s disease with normal immunoglobulin g level
x-linked agamaglobulinemia (xla) or bruton’s disease is a genetic disease resulting from a mutation in the bruton’s tyrosine kinase (btk) gene. this mutation leads to b cell arrest during differentiation (1). this disease was first described by ogden bruton in 1952 (2). approximately 85% of the affected subjects are male (3). this disorder is inherited as an x-linked recessive trait. carrier fe...
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Introduction:preeclampsia has remained one of the important obstetrical problems for which different factors have been suggested.decrease of serum levels of albumin,total protein and phosphorous have been suggested in the pathophysiology of precclampsia.the aim of this study was to determine serum levels of albumin,total protein and phosphorous in normal pregnancy and preeclamptic woman. Me...
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Cardiovascular diseases are a major cause of death worldwide. Endothelial dysfunction, inflammatory conditions, and oxidative stress at the forefront of the onset and progression of most cardiovascular diseases specificaly coronary heart disease and heart failure. Melatonin is a type of indole neuroendocrine hormone. It was first found that the regulation of the sleep-wake cycle is regulated...
متن کاملA case of Bruton's disease with normal immunoglobulin G level.
X-linked agamaglobulinemia (XLA) or Bruton’s disease is a genetic disease resulting from a mutation in the Bruton’s tyrosine kinase (Btk) gene. This mutation leads to B cell arrest during differentiation (1). This disease was first described by Ogden Bruton in 1952 (2). Approximately 85% of the affected subjects are male (3). This disorder is inherited as an X-linked recessive trait. Carrier fe...
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ژورنال
عنوان ژورنال: Endoscopy
سال: 2015
ISSN: 0013-726X,1438-8812
DOI: 10.1055/s-0034-1377983