{"id":1988,"date":"2022-09-06T14:27:37","date_gmt":"2022-09-06T14:27:37","guid":{"rendered":"https:\/\/neuropediatoolbox.org\/?p=1988"},"modified":"2026-06-22T20:07:37","modified_gmt":"2026-06-22T20:07:37","slug":"herencia-ligada-al-x-con-susceptibilidad-femenina","status":"publish","type":"post","link":"https:\/\/neuropediatoolkit.org\/fr\/herencia-ligada-al-x-con-susceptibilidad-femenina\/","title":{"rendered":"H\u00e9ritage li\u00e9 \u00e0 l'X avec susceptibilit\u00e9 f\u00e9minine."},"content":{"rendered":"\n<p>En la herencia ligada al X, cl\u00e1sicamente se ha considerado que el patr\u00f3n de transmisi\u00f3n se produce de mujeres portadoras a varones afectos, y que por tanto, una mujer portadora tendr\u00eda una probabilidad de concebir un 50% de varones afectos y un 50% de mujeres portadoras. Sin embargo este supuesto s\u00f3lo se cumple en el caso de enfermedades recesivas. <\/p>\n\n\n\n<p>Adem\u00e1s, existen determinadas circustancias que pueden dar lugar a un patr\u00f3n de herencia \u00abinvertido\u00bb, con mujeres afectas y hombres no afectos. Este fen\u00f3meno parad\u00f3jico se produce en varias enfermedades neurol\u00f3gicas relevantes, la m\u00e1s conocida el s\u00edndrome de Rett. <\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/books\/NBK1497\/\">S\u00edndrome de Rett (MeCP2).<\/a><\/li>\n\n\n\n<li><a href=\"http:\/\/epilepsygenetics.net\/2018\/02\/08\/pcdh19-related-epilepsy-understanding-cellular-interference\/\">Epilepsia relacionada con la PCDH19.<\/a><\/li>\n\n\n\n<li><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/books\/NBK561282\/\">Trastorno del neurodesarrollo relacionado con DDX3X. <\/a><\/li>\n\n\n\n<li><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/books\/NBK602610\/\" title=\"\">Trastorno del neurodesarrollo relacionado con CDKL5.<\/a><\/li>\n\n\n\n<li><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/books\/NBK1472\/\">Incontinentia pigmenti.<\/a><\/li>\n<\/ul>\n\n\n<div id=\"zotpress-aa20260bba92e9bf698474fdace59517\" class=\"zp-Zotpress zp-Zotpress-Bib 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id=\"zp-ID-1988-19955111-AK2B8TNZ\" data-zp-author-date='Migeon-2020-07' data-zp-date-author='2020-07-Migeon' data-zp-date='2020-07' data-zp-year='2020' data-zp-itemtype='journalArticle' class=\"zp-Entry zpSearchResultsItem\">\n<div class=\"csl-bib-body\" style=\"line-height: 1.35; \">\n  <div class=\"csl-entry\" style=\"clear: left; \">\n    <div class=\"csl-left-margin\" style=\"float: left; padding-right: 0.5em; text-align: right; width: 1em;\">1.<\/div><div class=\"csl-right-inline\" style=\"margin: 0 .4em 0 1.5em;\">Migeon BR. X-linked diseases: susceptible females. Genetics in Medicine [Internet]. 2020 July [cited 2021 Apr 5];22(7):1156\u201374. Available from: <a class='zp-ItemURL' href='https:\/\/www.nature.com\/articles\/s41436-020-0779-4'>https:\/\/www.nature.com\/articles\/s41436-020-0779-4<\/a><\/div>\n  <\/div>\n<\/div>\n\t\t\t\t<\/div><!-- .zp-Entry .zpSearchResultsItem -->\n\t\t\t<\/div><!-- .zp-zp-SEO-Content -->\n\t\t<\/div><!-- .zp-List -->\n\t<\/div><!--.zp-Zotpress-->\n\n\n","protected":false},"excerpt":{"rendered":"<p>Dans la transmission li\u00e9e \u00e0 l'X, on consid\u00e8re classiquement que le mode de transmission se produit des femmes porteuses aux hommes atteints, et que par cons\u00e9quent, une femme porteuse aurait 50 % de probabilit\u00e9 de concevoir des hommes atteints et 50 % des femmes porteuses. Cependant, cette hypoth\u00e8se n'est v\u00e9rifi\u00e9e que dans le... <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/neuropediatoolkit.org\/fr\/herencia-ligada-al-x-con-susceptibilidad-femenina\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> \u00abHerencia ligada al X con susceptibilidad femenina.\u00bb<\/span><\/a><\/p>","protected":false},"author":1,"featured_media":2267,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_themeisle_gutenberg_block_has_review":false,"footnotes":""},"categories":[44],"tags":[],"class_list":["post-1988","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-consejo-genetico-y-herencia","entry"],"_links":{"self":[{"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/posts\/1988","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/comments?post=1988"}],"version-history":[{"count":3,"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/posts\/1988\/revisions"}],"predecessor-version":[{"id":8472,"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/posts\/1988\/revisions\/8472"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/media\/2267"}],"wp:attachment":[{"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/media?parent=1988"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/categories?post=1988"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/neuropediatoolkit.org\/fr\/wp-json\/wp\/v2\/tags?post=1988"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}