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{{CMG}} [[Ogechukwu Hannah Nnabude, MD]]
 
==Overview==
Genetic and molecular tests can be useful in the diagnosis of [[adiposogenital dystrophy]].
 
==Other Diagnostic Findings==
Molecular and [[genetic testing]] for [[DNA methylation]] to rule out other similar diseases such as [[Prader-Willi syndrome]] and Bardet-Biedl syndrome<ref>Driscoll, D. J., Miller, J. L., Schwartz, S., & Cassidy, S. B. (1998). Prader-Willi Syndrome. In M. P. Adam (Eds.) et. al., GeneReviews®. University of Washington, Seattle.</ref> <ref>Bardet-biedl syndrome. Bissonnette B, & Luginbuehl I, & Marciniak B, & Dalens B.J.(Eds.), (2006). Syndromes: Rapid Recognition and Perioperative Implications. McGraw Hill. https://accessanesthesiology.mhmedical.com/content.aspx?bookid=852&sectionid=49517256</ref>
 
==References==
==References==
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[[Category:Needs content]]
[[Category:Disease]]
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[[Category:Genetic disorders]]

Latest revision as of 08:15, 29 December 2021

Adiposogenital dystrophy Microchapters

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Overview

Historical Perspective

Classification

Pathophysiology

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Differentiating Adiposogenital dystrophy from other Diseases

Epidemiology and Demographics

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Ogechukwu Hannah Nnabude, MD

Overview

Genetic and molecular tests can be useful in the diagnosis of adiposogenital dystrophy.

Other Diagnostic Findings

Molecular and genetic testing for DNA methylation to rule out other similar diseases such as Prader-Willi syndrome and Bardet-Biedl syndrome[1] [2]

References

  1. Driscoll, D. J., Miller, J. L., Schwartz, S., & Cassidy, S. B. (1998). Prader-Willi Syndrome. In M. P. Adam (Eds.) et. al., GeneReviews®. University of Washington, Seattle.
  2. Bardet-biedl syndrome. Bissonnette B, & Luginbuehl I, & Marciniak B, & Dalens B.J.(Eds.), (2006). Syndromes: Rapid Recognition and Perioperative Implications. McGraw Hill. https://accessanesthesiology.mhmedical.com/content.aspx?bookid=852&sectionid=49517256

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