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Prader Willi Syndrom - Versionsgeschichte
2026-08-13T13:59:20Z
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2013-02-19T13:10:04Z
<p>who Bx</p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Version vom 19. Februar 2013, 13:10 Uhr</td>
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<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">|01-CODE = Q 87.1</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">|01-BEZEICHNUNG = Prader-Willi Syndrom</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">}}</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Es wurde kürzlich gezeigt, dass scheinbar ähnliche Deletionen von Chromosom 15q treten häufig in der '''Prader-Willi'''-und das [[Angelman Syndrom|Angelman-Syndrom]]<ref>[http://onlinelibrary.wiley.com/doi/10.1002/ajmg.1320350307/abstract Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences American Journal of Medical Genetics 35:333 (1990)]</ref></div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Es wurde kürzlich gezeigt, dass scheinbar ähnliche Deletionen von Chromosom 15q treten häufig in der '''Prader-Willi'''-und das [[Angelman Syndrom|Angelman-Syndrom]]<ref>[http://onlinelibrary.wiley.com/doi/10.1002/ajmg.1320350307/abstract Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences American Journal of Medical Genetics 35:333 (1990)]</ref></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Die D15S9 und D15S63 Loci im Prader-Willi/Angelman Syndrom-Region auf Chromosom 15 unterliegen parent-of-origin-spezifische DNA-Methylierung. Zwei Prader-Willi-Syndrom Familien were gefunden, in denen die Patienten tragen eine mütterliche Methylierung Aufdruck auf dem väterlichen Chromosom gefunden. In einer dieser Familien besitzen die Patienten eine kleine Deletion umfasst, die das Gen für die kleine nukleare Ribonukleoprotein Polypeptid N, die 130 kb Telomer zu D15S63 abbildet.</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>Die D15S9 und D15S63 Loci im Prader-Willi/Angelman Syndrom-Region auf Chromosom 15 unterliegen parent-of-origin-spezifische DNA-Methylierung. Zwei Prader-Willi-Syndrom Familien were gefunden, in denen die Patienten tragen eine mütterliche Methylierung Aufdruck auf dem väterlichen Chromosom gefunden. In einer dieser Familien besitzen die Patienten eine kleine Deletion umfasst, die das Gen für die kleine nukleare Ribonukleoprotein Polypeptid N, die 130 kb Telomer zu D15S63 abbildet.</div></td></tr>
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Penarc: wLink
2013-02-19T13:05:26Z
<p>wLink</p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Version vom 19. Februar 2013, 13:05 Uhr</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[[Datei:pptpdtjpg1.png|miniatur|Entstehender Artikel]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[[Datei:pptpdtjpg1.png|miniatur|Entstehender Artikel]]</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Es wurde kürzlich gezeigt, dass scheinbar ähnliche Deletionen von Chromosom 15q treten häufig in der '''Prader-Willi'''-und das [[Angelman Syndrom|Angelman-Syndrom]]<ref>[http://onlinelibrary.wiley.com/doi/10.1002/ajmg.1320350307/abstract Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences American Journal of Medical Genetics 35:333 (1990)]</ref></ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Die D15S9 und D15S63 Loci im Prader-Willi/Angelman Syndrom-Region auf Chromosom 15 unterliegen parent-of-origin-spezifische DNA-Methylierung. Zwei Prader-Willi-Syndrom Familien were gefunden, in denen die Patienten tragen eine mütterliche Methylierung Aufdruck auf dem väterlichen Chromosom gefunden. In einer dieser Familien besitzen die Patienten eine kleine Deletion umfasst, die das Gen für die kleine nukleare Ribonukleoprotein Polypeptid N, die 130 kb Telomer zu D15S63 abbildet.</ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{| class="wikitable" |</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{| class="wikitable" |</div></td></tr>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Bibliographie ==</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Bibliographie ==</div></td></tr>
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Penarc: Rfz9
2011-03-18T16:42:25Z
<p>Rfz9</p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Version vom 18. März 2011, 16:42 Uhr</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{| class="wikitable" |</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{| class="wikitable" |</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| bgcolor="#dfdfdf" | '''Freie Übersichtsartikel'''</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| bgcolor="#dfdfdf" | '''Freie Übersichtsartikel'''</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>| align="left" width="800" |<ref name="PMID11739333">Endocrine dysfunction in Prader-Willi syndrome: a review with special reference to GH. Endocr Rev 22(6):787-99 (2001) PMID 11739333 </ref><ref name="PMID12651746">Growth hormone therapy in the Prader-Willi syndrome. Arch Dis Child 88(4):283-5 (2003) PMID 12651746 </ref><ref name="PMID10469839">Towards a molecular understanding of Prader-Willi and Angelman syndromes. Hum Mol Genet 8(10):1867-73 (1999) PMID 10469839 </ref><ref name="PMID18697869">Recommendations for the diagnosis and management of Prader-Willi syndrome. J Clin Endocrinol Metab 93(11):4183-97 (2008) PMID 18697869 </ref><ref name="PMID9391886">Prader-Willi syndrome. J Med Genet 34(11):917-23 (1997) PMID 9391886 </ref><ref name="PMID933113">The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature. J Med Genet 13(2):152-7 (1976) PMID 933113 </ref><ref name="PMID11694676">The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria. Pediatrics 108(5):E92 (2001) PMID 11694676 </ref><ref name="PMID811011">[The effect of lead on cells cultivated in vitro. I. Acute effects (author's transl)] Zentralbl Bakteriol Orig B 161(1):26-37 (1975) PMID 811011 </ref></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>| align="left" width="800" |<ref name="PMID11739333">Endocrine dysfunction in Prader-Willi syndrome: a review with special reference to GH. Endocr Rev 22(6):787-99 (2001) PMID 11739333 </ref><ref name="PMID12651746">Growth hormone therapy in the Prader-Willi syndrome. Arch Dis Child 88(4):283-5 (2003) PMID 12651746 </ref><ref name="PMID10469839">Towards a molecular understanding of Prader-Willi and Angelman syndromes. Hum Mol Genet 8(10):1867-73 (1999) PMID 10469839 </ref><ref name="PMID18697869">Recommendations for the diagnosis and management of Prader-Willi syndrome. J Clin Endocrinol Metab 93(11):4183-97 (2008) PMID 18697869 </ref><ref name="PMID9391886">Prader-Willi syndrome. J Med Genet 34(11):917-23 (1997) PMID 9391886 </ref><ref name="PMID933113">The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature. J Med Genet 13(2):152-7 (1976) PMID 933113 </ref><ref name="PMID11694676">The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria. Pediatrics 108(5):E92 (2001) PMID 11694676 </ref><ref name="PMID811011">[The effect of lead on cells cultivated in vitro. I. Acute effects (author's transl)] Zentralbl Bakteriol Orig B 161(1):26-37 (1975) PMID 811011 </ref><ins style="font-weight: bold; text-decoration: none;"><ref>Which Neurodevelopmental Disorders Get Researched and Why? [http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0015112 PLoS ONE 5(11): e15112]. doi:10.1371/journal.pone.0015112 </ref></ins></div></td></tr>
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Ossip Groth: hat „Prader-Willi-Syndrom“ nach „Prader Willi Syndrom“ verschoben
2010-06-22T16:44:43Z
<p>hat „<a href="/wiki/Prader-Willi-Syndrom" class="mw-redirect" title="Prader-Willi-Syndrom">Prader-Willi-Syndrom</a>“ nach „<a href="/wiki/Prader_Willi_Syndrom" title="Prader Willi Syndrom">Prader Willi Syndrom</a>“ verschoben</p>
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<td colspan="1" style="background-color: #fff; color: #202122; text-align: center;">Version vom 22. Juni 2010, 16:44 Uhr</td>
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Ossip Groth
https://ddn.pluspedia.org/w/index.php?title=Prader_Willi_Syndrom&diff=43845&oldid=prev
Ossip Groth am 15. April 2010 um 14:53 Uhr
2010-04-15T14:53:24Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Version vom 15. April 2010, 14:53 Uhr</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| bgcolor="#dfdfdf" | '''Freie Übersichtsartikel'''</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| bgcolor="#dfdfdf" | '''Freie Übersichtsartikel'''</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>| align="left" width="800" |<ref name="PMID11739333"><del style="font-weight: bold; text-decoration: none;">. et al., </del>Endocrine dysfunction in Prader-Willi syndrome: a review with special reference to GH. Endocr Rev 22(6):787-99 (2001) PMID 11739333 </ref></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>| align="left" width="800" |<ref name="PMID11739333">Endocrine dysfunction in Prader-Willi syndrome: a review with special reference to GH. Endocr Rev 22(6):787-99 (2001) PMID 11739333 </ref><ins style="font-weight: bold; text-decoration: none;"><ref name="PMID12651746">Growth hormone therapy in the Prader-Willi syndrome. Arch Dis Child 88(4):283-5 (2003) PMID 12651746 </ref><ref name="PMID10469839">Towards a molecular understanding of Prader-Willi and Angelman syndromes. Hum Mol Genet 8(10):1867-73 (1999) PMID 10469839 </ref><ref name="PMID18697869">Recommendations for the diagnosis and management of Prader-Willi syndrome. J Clin Endocrinol Metab 93(11):4183-97 (2008) PMID 18697869 </ref><ref name="PMID9391886">Prader-Willi syndrome. J Med Genet 34(11):917-23 (1997) PMID 9391886 </ref><ref name="PMID933113">The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature. J Med Genet 13(2):152-7 (1976) PMID 933113 </ref><ref name="PMID11694676">The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria. Pediatrics 108(5):E92 (2001) PMID 11694676 </ref><ref name="PMID811011">[The effect of lead on cells cultivated in vitro. I. Acute effects (author's transl)] Zentralbl Bakteriol Orig B 161(1):26-37 (1975) PMID 811011 </ref></ins></div></td></tr>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Bibliographie ==</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Bibliographie ==</div></td></tr>
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Ossip Groth
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| align="left" width="800" |<ref name="PMID11739333">. et al., Endocrine dysfunction in Prader-Willi syndrome: a review with special reference to GH. Endocr Rev 22(6):787-99 (2001) PMID 11739333 </ref><br />
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== Bibliographie ==<br />
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Ossip Groth