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Trophoblast‐specific expression of HLA‐G induces immune tolerance for the developing fetus. Pathological HLA‐G expression later in life might contribute to immune escape of various cancers. We studied the still controversial role of HLA‐G in colorectal carcinoma (CRC) using the MEM‐G/1 antibody and a tissue microarray series of CRC tumors (n = 317). HLA‐G expression appeared in 20% of the tumors and...
Congenital chloride diarrhoea (CLD) is a rare autosomal recessive disease with chronic secretory diarrhoea and a need for lifelong salt replacement therapy. We describe a male newborn of consanguineous parents with CLD. Postnatally, frequent watery diarrhoea and electrolyte disturbances were noted from the day 8 of his life. At molecular level, a homozygous mutation was detected in the solute carrier...
Congenital chloride diarrhea (CLD) is an autosomal recessive disorder with around 250 cases reported so far. Life‐long secretory diarrhea is caused by mutations in the solute carrier family 26 member 3 (SLC26A3) gene disrupting the epithelial Cl−/HCO transport in the ileum and colon. Although salt substitution allows favorable outcome, possible manifestations include renal impairment, intestinal...
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