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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...
Tallennettuna:
| Julkaisussa: | JPRAS Open |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Elsevier
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8027531/ https://ncbi.nlm.nih.gov/pubmed/33855151 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jpra.2021.03.001 |
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