SUN-332: A Rare Case of Hereditary 1,25 (OH)2D Resistant Rickets

    October 2024 in “ Journal of the Endocrine Society
    Gunjan Umarji, Franklin Thelmo, Serge Jabbour
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    Studysummary This study highlights a rare case of vitamin D-dependent rickets type 2A caused by a heterozygous mutation in the vitamin D receptor gene, emphasizing the complexity of managing this condition with high-dose calcium and vitamin D therapy.
    Automatically generated from the study's abstract, not written by a person, and not a review of the full paper. Not medical advice or a treatment recommendation. Read the original study, and consult a qualified healthcare professional before changing treatment. Full disclaimer
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