HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Chronic diarrhea and juvenile cataracts: think cerebrotendinous xanthomatosis and treat.

Abstract
Cerebrotendinous xanthomatosis is an autosomal recessive disease of bile acid synthesis caused by 27-hydroxylase deficiency. Treatment with chenodeoxycholic acid normalizes cholestanol concentrations and abrogates progression of the disease. We present 4 patients with cerebrotendinous xanthomatosis within 1 family who were treated with chenodeoxycholic acid for 14 years. Two young sisters started treatment at the preclinical stage before the appearance of major symptoms. Their 2 older uncles, who had already developed the complete phenotypic form of cerebrotendinous xanthomatosis when diagnosed, commenced treatment at the same time as the sisters, thus establishing a natural control group. After 14 years of chenodeoxycholic acid therapy, the cholestanol levels of all 4 patients decreased to normal levels (<6 microg/mL). Both sisters remained asymptomatic. Only moderate improvement in symptoms was observed in their uncles. In this long-term study, prompt preclinical administration of chenodeoxycholic acid in early childhood completely prevented the cerebrotendinous xanthomatosis phenotype in 2 sisters. Pediatricians should be aware of this diagnostic possibility of cerebrotendinous xanthomatosis in children presenting with chronic diarrhea and juvenile cataracts. Prevention is particularly significant in light of the availability of early genetic diagnosis and the devastating effects of this illness if not treated.
AuthorsVladimir M Berginer, Bella Gross, Khayat Morad, Nechama Kfir, Siman Morkos, Salameh Aaref, Tzipora C Falik-Zaccai
JournalPediatrics (Pediatrics) Vol. 123 Issue 1 Pg. 143-7 (Jan 2009) ISSN: 1098-4275 [Electronic] United States
PMID19117873 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Bile Acids and Salts
  • Chenodeoxycholic Acid
Topics
  • Adolescent
  • Adult
  • Bile Acids and Salts (antagonists & inhibitors, biosynthesis)
  • Cataract (diagnosis, drug therapy, genetics)
  • Chenodeoxycholic Acid (therapeutic use)
  • Child, Preschool
  • Chronic Disease
  • Diagnosis, Differential
  • Diarrhea (diagnosis, drug therapy, genetics)
  • Female
  • Humans
  • Male
  • Mutation
  • Pedigree
  • Prevalence
  • Time
  • Xanthomatosis, Cerebrotendinous (diagnosis, drug therapy, epidemiology, genetics)
  • Young Adult

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: