Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome

BACKGROUND: 22q11·2 deletion syndrome (22q11·2DS) is a relatively common yet under-recognized genetic syndrome that may present with endocrine features. We aimed to address the factors that contribute to the high prevalence of hypocalcaemia. METHODS: We investigated hypocalcaemia in a well-character...

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Detalles Bibliográficos
Autores principales: Cheung, Evelyn Ning Man, George, Susan R, Costain, Gary A, Andrade, Danielle M, Chow, Eva W C, Silversides, Candice K, Bassett, Anne S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231257/
https://www.ncbi.nlm.nih.gov/pubmed/24735350
http://dx.doi.org/10.1111/cen.12466

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231257/
https://www.ncbi.nlm.nih.gov/pubmed/24735350
http://dx.doi.org/10.1111/cen.12466

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