Talk:Kabuki syndrome
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Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about Kabuki syndrome.
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PMID links to the record in PubMed. Linked article titles go to the free full text in PubMed Central.
Systematic Reviews
[edit]- Xin et al. (2018) Identification of novel KMT2D mutations in two Chinese children with Kabuki syndrome: a case report and systematic literature review. PMID: 29482518)
- Liu et al. (2015) Kabuki syndrome: a Chinese case series and systematic review of the spectrum of mutations. PMID: 25896430
Recent Reviews
[edit]- Adli et al. (2014) Diverse functions of PHD fingers of the MLL/KMT2 subfamily. PMID: 24291127
- Bögershausen et al. (2016) Mutation Update for Kabuki Syndrome Genes KMT2D and KDM6A and Further Delineation of X-Linked Kabuki Syndrome Subtype 2. PMID: 27302555
- Bokinni Y. (2012) Kabuki syndrome revisited. PMID: 22437206
- Cheon & Ko. (2015) Kabuki syndrome: clinical and molecular characteristics. PMID: 26512256
- Dentici et al. (2015) Kabuki syndrome: clinical and molecular diagnosis in the first year of life. PMID: 25281733
- Digilio & Marino. (2016) What Is New in Genetics of Congenital Heart Defects? PMID: 27990414
- Lederer et al. (2014) A three generation X-linked family with Kabuki syndrome phenotype and a frameshift mutation in KDM6A. PMID: 24664873
- Lintas & Persico. (2017) Unraveling molecular pathways shared by Kabuki and Kabuki-like syndromes. PMID: 28139835
- Rangasamy et al. (2013) Epigenetics, autism spectrum, and neurodevelopmental disorders. PMID: 24104594
- Sobreira et al. (2017) Patients with a Kabuki syndrome phenotype demonstrate DNA methylation abnormalities. PMID: 29255178
- Stagi et al. (2016) Epigenetic control of the immune system: a lesson from Kabuki syndrome. PMID: 26411453
- Van der Meulen et al. (2014) The H3K27me3 demethylase UTX in normal development and disease. PMID: 24561908
- Yang et al. (2016) De novo exonic deletion of KDM6A in a Chinese girl with Kabuki syndrome: A case report and brief literature review. PMID: 2702810
- Yuan SM. (2013) Congenital heart defects in Kabuki syndrome. PMID: 23558868
- Zollino et al. (2017) Syndromic Craniosynostosis Can Define New Candidate Genes for Suture Development or Result from the Non-specifc Effects of Pleiotropic Genes: Rasopathies and Chromatinopathies as Examples. PMID: 29093661
National Library of Medicine on Kabuki syndrome
[edit]- GARD (Genetic and Rare Diseases Information Center) - NIH Center for Advancing Translational Sciences
- GeneReviews - Clinically relevant and medically actionable information for inherited conditions
- Genetics Home Reference - Kabuki Syndrome page
- Genetics Home Reference - KDM6A gene
- Genetics Home Reference - KMT2D gene
- MedGen - Clinical information about medical genetics phenotypes including Mendelian disorders, complex diseases, clinical features and pharmacogenetics
Errors/Terminology
[edit]The external link on this page contradicts the shortened lifespan statement on this page, claiming there's no data to point to shortened lifespans. Can we resolve this conflict? EddEdmondson 14:42, 9 Jul 2004 (UTC)
Eponyms are things with the name of a famous/historical person attached (not a famous/historical thing). So does the "eponymous diseases" category really belong here? Kabuki is a form of theatre, not a person, as far as I know... - Nunh-huh 14:50, 9 Jul 2004 (UTC)
- I think, in medicine, the usage of "eponymous" expands a bit in medicine. For example, Alice in Wonderland syndrome is named after a fictional/fantasy location but how else do you want to classify it? Alex.tan 15:08, 15 Sep 2004 (UTC)
Merger with Niikawa-Kuroki Syndrome
[edit]Which page should be used as the main and which as the redirect? perhaps Kabuki syndrome is the better known. --apers0n 11:27, 29 June 2006 (UTC)
#CiteNLM2018 Edit-a-Thon
[edit]I am working on this page as part of the #CiteNLM2018 Edit-a-Thon. The goal is to cite in accordance with WikiProject Medicine guidelines for sources. Clearlykrystal (talk) 20:28, 15 April 2018 (UTC)
New & Expanded Sections
[edit]New sections to consider adding to the page:
- history
- further reading
Expand these sections to enrich page content:
- pathophysiology
- screening
- diagnosis
- management
- prognosis
- research directions
- external links Clearlykrystal (talk) 17:58, 20 April 2018 (UTC)