22q11.2 deletion syndrome risk factors: Difference between revisions
Jump to navigation
Jump to search
mNo edit summary |
Ayushijain (talk | contribs) |
||
| Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
{{22q11.2 deletion syndrome}} | {{22q11.2 deletion syndrome}} | ||
{{CMG}} {{AE}} | {{CMG}} {{AE}} | ||
==Overview== | ==Overview== | ||
The only known risk factor is that of a family history of DGS. | |||
==Risk Factors== | ==Risk Factors== | ||
A detailed history may reveal : | |||
* Family history of diagnosed or suspected DGS | |||
* Abnormal genetic testing results of family members | |||
==References== | ==References== | ||
Revision as of 18:42, 10 July 2020
|
22q11.2 deletion syndrome Microchapters |
|
Differentiating 22q11.2 deletion syndrome from other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
22q11.2 deletion syndrome risk factors On the Web |
|
American Roentgen Ray Society Images of 22q11.2 deletion syndrome risk factors |
|
Risk calculators and risk factors for 22q11.2 deletion syndrome risk factors |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief:
Overview
The only known risk factor is that of a family history of DGS.
Risk Factors
A detailed history may reveal :
- Family history of diagnosed or suspected DGS
- Abnormal genetic testing results of family members