Camptodactyly and DiGeorge syndrome: A rare hand anomaly

The most common deletion syndrome is 22q11.2 and it effects an estimated 1 in 3000 live births. Major features of this multisystem condition include congenital abnormalities, developmental delay, learning difficulties, immunodeficiency, endocrine anomalies and an array of psychiatric disorders. Howe...

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Detalles Bibliográficos
Autores principales: Hurley, C.M., McHugh, N., Carr, S., Kelly, J.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027531/
https://www.ncbi.nlm.nih.gov/pubmed/33855151
http://dx.doi.org/10.1016/j.jpra.2021.03.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027531/
https://www.ncbi.nlm.nih.gov/pubmed/33855151
http://dx.doi.org/10.1016/j.jpra.2021.03.001

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