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Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome)
Deletion 22q11.2 syndrome (Del22) (DiGeorge/Velo-Cardio-Facial syndrome) is characterized by congenital heart defect (CHD), palatal anomalies, facial dysmorphisms, neonatal hypocalcemia, immune deficit, speech and learning disabilities. CHD is present in 75% of patients with Del22. The most frequent...
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| Fformat: | Artigo |
| Iaith: | Inglês |
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Medknow Publications & Media Pvt Ltd
2005
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| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3232571/ https://ncbi.nlm.nih.gov/pubmed/22368650 |
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