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Results 1 - 6 of 6 for Cobalamin deficiency
Did you mean calamine deficiency?
  1. Methylmalonic acidemia with homocystinuria 
    ... Huemer M, Baumgartner MR. The clinical presentation of cobalamin-related disorders: From acquired deficiencies to inborn errors of absorption and intracellular pathways. ...
    https://medlineplus.gov/...ethylmalonic-acidemia-with-homocystinuria - Genetics
  2. Transcobalamin deficiency 
    Transcobalamin deficiency is a disorder that impairs the transport of cobalamin (also known as vitamin B12) within the body. Cobalamin is obtained from the diet; this vitamin is ...
    https://medlineplus.gov/genetics/condition/transcobalamin-deficiency - Genetics
  3. Glutamate formiminotransferase deficiency 
    ... PubMed Whitehead VM. Acquired and inherited disorders of cobalamin and folate in children. Br J Haematol. 2006 Jul;134(2):125-36. doi: 10.1111/j.1365-2141.2006.06133.x. Citation on PubMed
    https://medlineplus.gov/...glutamate-formiminotransferase-deficiency - Genetics
  4. Holocarboxylase synthetase deficiency 
    ... Antenatal and postnatal radiologic diagnosis of holocarboxylase synthetase deficiency: a ... disorders: cobalamin, folate, biotin, vitamins B1 and E. Handb Clin ...
    https://medlineplus.gov/.../holocarboxylase-synthetase-deficiency - Genetics
  5. Homocystinuria 
    ... Levy HL. Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency. 2004 ... Inherited defects of cobalamin metabolism. Vitam Horm. 2022;119:355-376. doi: ...
    https://medlineplus.gov/genetics/condition/homocystinuria - Genetics
  6. Methylmalonic acidemia 
    ... This enzyme works with vitamin B12 (also called cobalamin) to break down several protein ... Genetic Testing Registry: Methylmalonic aciduria, cblA type Genetic ...
    https://medlineplus.gov/genetics/condition/methylmalonic-acidemia - Genetics