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. 2022 Feb 7;8(4):181-182.

doi: 10.1016/j.aace.2022.02.001. eCollection 2022 Jul-Aug.

Newly Diagnosed Hypoparathyroidism as the Initial Presentation of DiGeorge Syndrome in a 26-Year-Old Man

Anvay Shah¹, Bridget Sinnott¹

Affiliations

PMID: 35959083
PMCID: PMC9363511
DOI: 10.1016/j.aace.2022.02.001

Newly Diagnosed Hypoparathyroidism as the Initial Presentation of DiGeorge Syndrome in a 26-Year-Old Man

Anvay Shah et al. AACE Clin Case Rep. 2022.

. 2022 Feb 7;8(4):181-182.

doi: 10.1016/j.aace.2022.02.001. eCollection 2022 Jul-Aug.

Authors

Anvay Shah¹, Bridget Sinnott¹

Affiliation

¹ Division of Endocrinology, Diabetes and Metabolism, Medical College of Georgia, Augusta, Georgia.

PMID: 35959083
PMCID: PMC9363511
DOI: 10.1016/j.aace.2022.02.001

No abstract available

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References

1. Cohen E., Chow E.W., Weksberg R., Bassett A.S. Phenotype of adults with the 22q11 deletion syndrome: a review. Am J Med Genet. 1999;86(4):359–365. - PMC - PubMed
1. McDonald-McGinn D.M., Reilly A., Wallgren-Pettersson C., et al. Malignancy in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) Am J Med Genet A. 2006;140(8):906–909. - PubMed
1. Lambert M.P., Arulselvan A., Schott A., et al. The 22q11.2 deletion syndrome: cancer predisposition, platelet abnormalities and cytopenias. Am J Med Genet A. 2018;176(10):2121–2127. - PubMed

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