Methylmalonic acidemia with homocystinuria, type cblF
Other Names for this Disease
- CblF defect
- Cobalamin F defect
- Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblF
- Lysosomal membrane cobalamin transporter deficiency
- Methylmalonic acidemia with homocystinuria type cblF
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Treatment for methylmalonic aciduria with homocystinuria cbl f may involve a combination of vitamin B12 injections and dietary management such as a low-protein diet and medical formula. The following fact sheet for parents prepared by Screening, Technology and Research in Genetics provides additional information on the treatment and management of methylmalonic aciduria with homocystinuria. http://www.newbornscreening.info/Parents/organicaciddisorders/MMA_HCU.html#4
Last updated: 3/5/2014
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|Treatment of homocystinuria to decrease elevated homocysteine blood levels.|
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