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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2021
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| Materias: | |
| 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 |