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spermatocele/driska

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ČlankiKliničnih preskušanjPatenti
2 rezultatov

Long-term clinical outcome in patients with congenital chloride diarrhea.

Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
OBJECTIVE Congenital chloride diarrhea (CLD) is a rare, autosomal recessive disorder of intestinal Cl/HCO3 exchange caused by mutations in the SLC26A3 gene and characterized by persistent Cl rich diarrhea from birth. Treatment is symptomatic and replacement therapy with NaCl and KCl has been shown

Disruption of the SLC26A3-mediated anion transport is associated with male subfertility.

Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Male subfertility in congenital chloride diarrhea (CLD) was possible after identification of expression of an epithelial Cl-/HCO3- exchanger SLC26A3 in the male reproductive tract and by the observation that adult men with CLD had very few children. A prospective clinical and laboratory study among
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