Adiposogenital dystrophy other diagnostic studies: Difference between revisions
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==Overview== | ==Overview== | ||
Genetic and molecular tests can be useful in the diagnosis of [[adiposogenital dystrophy]]. | |||
==Other Diagnostic Findings== | ==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§ionid=49517256</ref> | |||
==References== | ==References== | ||
Latest revision as of 08:15, 29 December 2021
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Adiposogenital dystrophy Microchapters |
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Differentiating Adiposogenital dystrophy from other Diseases |
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Adiposogenital dystrophy other diagnostic studies On the Web |
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Risk calculators and risk factors for Adiposogenital dystrophy other diagnostic studies |
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
- ↑ 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.
- ↑ 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§ionid=49517256