22q11.2 deletion syndrome risk factors: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{22q11.2 deletion syndrome}} | {{22q11.2 deletion syndrome}} | ||
{{CMG}} {{AE}} {{ajane}} | |||
==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 | |||
==References== | ==References== | ||
{{ | {{reflist|2}} | ||
[[Category: | [[Category:Hematology]] | ||
{{WS}} | |||
{{WH}} | {{WH}} | ||
Latest revision as of 18:43, 10 July 2020
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22q11.2 deletion syndrome Microchapters |
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Differentiating 22q11.2 deletion syndrome from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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22q11.2 deletion syndrome risk factors On the Web |
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American Roentgen Ray Society Images of 22q11.2 deletion syndrome risk factors |
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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: Ayushi Jain, M.B.B.S[2]
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