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Congenital chloride diarrhea (CCD, also congenital chloridorrhea or Darrow Gamble syndrome) is a genetic disorder due to an autosomal recessive mutation on chromosome 7. The mutation is in downregulated-in-adenoma (DRA), a gene that encodes a membrane protein of intestinal cells .
Congenital chloride diarrhea, a lifelong condition caused by a genetic mutation that leads to diarrhea with a high concentration of chloride. [21] Congenital sodium diarrhea, a genetic disorder caused by mutations in electrolyte transporters that disrupt the transport of Na + across the intestine and results in high levels of Na + greater than ...
Congenital tufting enteropathy is an inherited disorder of the small intestine that presents with intractable diarrhea in young children. Signs and symptoms [ edit ]
Congenital chloride diarrhea; Congenital disorder of glycosylation type IIc; Congenital hyperinsulinism; Congenital ichthyosiform erythroderma; Congenital insensitivity to pain; Congenital insensitivity to pain with anhidrosis; Congenital lactic acidosis; Congenital stromal corneal dystrophy; Conjoined twins; Copenhagen disease; Corticobasal ...
The risk of congenital infection is highest during the first trimester (< 12 weeks). Risk of congenital rubella is increased among immigrant women from countries without adequate vaccination programs. Common symptoms include cataracts, hearing impairment, developmental delay and congenital heart disease. [18]
Common symptoms include increased rates of diarrhea. Zinc deficiency affects the skin and gastrointestinal tract; brain and central nervous system, immune, skeletal, and reproductive systems. Zinc deficiency in humans is caused by reduced dietary intake, inadequate absorption, increased loss, or increased body system use.