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Yonsei Medical Journal ; : 923-927, 2003.
Article in English | WPRIM | ID: wpr-205353

ABSTRACT

Vitamin K is the cofactor for the hepatic carboxylation of glutamic acid residues in a number of proteins including the procoagulants factors ll, Vll, lX, and X. The role of vitamin K in normal bone function is not fully understood. Inherited deficiency of vitamin K dependent coagulation factors is a rare bleeding disorder reported only in a few patients. Here we present an 18-month old child who presented with osteopeni due to inherited vitamin K deficiency. While the patient had high bone specific alkaline phosphatase and parathyroid hormone levels and low osteocalcin and bone mineral density values, with the regular supplementation of vitamin K all the mentioned parameters returned to normal values.


Subject(s)
Humans , Infant , Male , Bone Density , Bone Diseases, Metabolic/etiology , Osteocalcin/blood , Prothrombin Time , Vitamin K Deficiency/blood
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