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Literature summary for 1.1.1.145 extracted from

  • Nittono, H.; Takei, H.; Unno, A.; Shimizu, T.; Kobayashi, M.; Koike, M.; Murai, T.; Kurosawa, T.; Thoma, M.
    3?-hydroxy-??-C??-steroid dehydrogenase/isomerase deficiency in a patient who underwent oral bile acid therapy for 10 years and delivered two healthy infants. (2010), Pediatr. Internat., 52, e192-e195.
    View publication on PubMed

Application

Application Comment Organism
medicine patient with inborn error of bile acid metabolism, that is, 3beta-hydroxy-DELTA5-C27-steroid dehydrogenase/isomerase deficienc, receives as treatment chenodeoxycholic acid and cholic acid, orally administered for 10 years. After the oral bile acid therapy, the biochemical liver function values and serum alanine aminotransferase and total bilirubin levels are maintained at normal levels, while the 3beta,7alpha-dihydroxy- and 3beta,7alpha,12alpha-trihydroxy-5-cholenoic acid levels significantly decrease. The patient gave birth to a healthy boy and a girl during the 10-year follow-up period Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
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