DiGeorge anomaly (DGA) represents a heterogeneous entity, which is often sporadic, although familial cases and the association with monosomy 22q11 have been reported. Recently, a few patients with 10p deletion syndrome and immunological and other laboratory findings similar to DGA have been described. We report on an additional case of partial DGA associated with 10p deletion.
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1002/ajmg.1320390220 | DOI Listing |
Publication Analysis
Top Keywords
10p deletion
12
digeorge anomaly
8
associated 10p
8
anomaly associated
4
deletion digeorge
4
anomaly dga
4
dga represents
4
represents heterogeneous
4
heterogeneous entity
4
entity sporadic
4
Similar Publications
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!