{"id":22650,"date":"2026-04-27T10:05:03","date_gmt":"2026-04-27T09:05:03","guid":{"rendered":"https:\/\/www.trakgene.com\/?p=22650"},"modified":"2026-04-27T10:05:03","modified_gmt":"2026-04-27T09:05:03","slug":"master-the-pedigree-of-duchenne-muscular-dystrophy-a-complete-tutorial","status":"publish","type":"post","link":"https:\/\/www.trakgene.com\/cy\/2026\/04\/27\/master-the-pedigree-of-duchenne-muscular-dystrophy-a-complete-tutorial\/","title":{"rendered":"Master the Pedigree of Duchenne Muscular Dystrophy: A Complete Tutorial"},"content":{"rendered":"<h2 id=\"introduction\">Introduction<\/h2>\n<p>Duchenne Muscular Dystrophy (DMD) presents significant challenges for affected families, particularly in understanding its genetic inheritance. Grasping the genetic inheritance patterns of DMD is essential for informed medical decisions and effective family planning. Families must navigate the complexities of DMD to make informed choices for future generations, utilizing available resources and tools. By equipping themselves with knowledge and resources, families can make informed decisions that positively impact future generations.<\/p>\n<h2 id=\"explain-duchenne-muscular-dystrophy-and-its-inheritance-patterns\">Explain Duchenne Muscular Dystrophy and Its Inheritance Patterns<\/h2>\n<p><a href=\"https:\/\/www.trakgene.com\/cy\/\" target=\"_blank\" rel=\"noopener\">Duchenne Muscular Dystrophy<\/a> (DMD) presents significant challenges for affected families, particularly due to its complex <a href=\"https:\/\/mda.org\/disease\/duchenne-muscular-dystrophy\/causes-inheritance\" rel=\"noopener noreferrer nofollow\" target=\"_blank\">inheritance patterns<\/a> and severe physical implications. DMD poses severe challenges, primarily affecting boys. It is marked by <a href=\"https:\/\/www.trakgene.com\/cy\/2026\/02\/28\/understanding-non-mendelian-inheritance-definition-and-its-importance\/\">muscle degeneration<\/a> and weakness caused by mutations in the dystrophin gene on the X chromosome. This condition follows an X-linked recessive inheritance pattern. While females can carry the mutation, they typically do not show symptoms. Understanding the <a href=\"https:\/\/www.trakgene.com\/cy\/\" target=\"_blank\" rel=\"noopener\">pedigree of Duchenne muscular dystrophy<\/a> and its inheritance patterns is vital for <a href=\"https:\/\/www.trakgene.com\/cy\/\" target=\"_blank\" rel=\"noopener\">genetic counseling<\/a>. It helps evaluate the risk of DMD in future generations and informs family planning.<\/p>\n<p>Research shows that most mutations in the DMD gene are deletions, which can greatly influence the disorder&#8217;s severity. The EXPLORE44\u00ae trial demonstrated unprecedented delivery of phosphorodiamidate morpholino oligomers (PMOs) to skeletal muscle, resulting in significant increases in dystrophin production, showcasing the potential for innovative therapies. Ongoing studies stress the importance of <a href=\"https:\/\/musculardystrophynews.com\/news\/mds-2026-duvyzat-shows-dmd-benefits-even-lower-dose-levels\" rel=\"noopener noreferrer nofollow\" target=\"_blank\">early interventions<\/a>, like corticosteroid treatment, which can enhance motor function in DMD patients.<\/p>\n<p>Genetic counselors are essential in navigating the complexities of the pedigree of Duchenne muscular dystrophy inheritance. They help families understand <a href=\"https:\/\/www.trakgene.com\/cy\/2026\/03\/04\/4-free-pedigree-makers-for-genetic-counselors-to-streamline-work\/\">carrier status<\/a> and the risks for future children. Examples of genetic counseling for DMD show the emotional and practical support available to families facing this diagnosis. Understanding DMD not only informs medical decisions but also profoundly impacts the <a href=\"https:\/\/parentprojectmd.org\/news\" rel=\"noopener noreferrer nofollow\" target=\"_blank\">emotional landscape<\/a> of families facing this diagnosis.<\/p>\n<p><img decoding=\"async\" alt=\"This mindmap starts with DMD at the center, branching out to show how it affects families, the inheritance patterns involved, and the importance of genetic counseling. Each branch represents a different aspect of DMD, making it easier to see how they connect and the overall impact on families.\" src=\"https:\/\/images.tely.ai\/telyai\/zrgkppsv-this-mindmap-starts-with-dmd-at-the-center-branching-out-to-show-how-it-affects-families-the-inheritance-patterns-involved-and-the-importance-of-genetic-counseling-each-branch-represents-a-different-aspect-of-dmd-making-it-easier-to-see-how-they-connect-and-the-overall-impact-on-families.webp\" title=\"This mindmap starts with DMD at the center, branching out to show how it affects families, the inheritance patterns involved, and the importance of genetic counseling. Each branch represents a different aspect of DMD, making it easier to see how they connect and the overall impact on families.\" \/><\/p>\n<h2 id=\"construct-a-pedigree-chart-for-dmd-step-by-step-guide\">Construct a Pedigree Chart for DMD: Step-by-Step Guide<\/h2>\n<p>Accurate <a href=\"https:\/\/www.trakgene.com\/cy\/\" target=\"_blank\" rel=\"noopener\">family health history<\/a> is essential for understanding the implications of the pedigree of Duchenne muscular dystrophy (DMD).<\/p>\n<ol>\n<li>Gather Relative Information: Begin by collecting comprehensive details about relatives, including names, birth dates, and <a href=\"https:\/\/www.trakgene.com\/cy\/2026\/02\/03\/10-top-genetic-counseling-programs-in-california-for-future-counselors\/\">health histories related to DMD<\/a>. Engaging in discussions with relatives can be challenging, especially when it involves sensitive health histories, but it is crucial for a <a href=\"https:\/\/www.trakgene.com\/cy\/2026\/03\/12\/best-practices-for-effective-pedigree-drawing-software-referral\/\">thorough understanding of the medical background<\/a>.<\/li>\n<li>Choose Symbols: Familiarize yourself with the standard symbols used in <a href=\"https:\/\/www.trakgene.com\/cy\/\" target=\"_blank\" rel=\"noopener\">pedigree charts<\/a>: squares represent males, circles represent females, filled shapes signify affected individuals, and lines depict relationships &#8211; horizontal lines for marriages and vertical lines for offspring. Clear symbols are essential for accurately representing relationships.<\/li>\n<li>Map Generations: Arrange relatives into generations, placing the oldest generation at the top and moving downwards. Clearly separate each generation to prevent confusion, using Roman numerals to denote <a href=\"https:\/\/www.trakgene.com\/cy\/2026\/02\/15\/4-steps-to-discuss-medical-family-history-effectively\/\">generational levels<\/a>. This structured approach aids in understanding lineage.<\/li>\n<li>Indicate Relationships: Draw lines to connect individuals based on their relationships. For instance, connect parents with a horizontal line and extend vertical lines down to their children. This <a href=\"https:\/\/opengenetics.pressbooks.tru.ca\/chapter\/pedigree-analysis\" rel=\"noopener noreferrer nofollow\" target=\"_blank\">visual mapping helps clarify relational dynamics<\/a> and lineage.<\/li>\n<li>Mark Influenced Individuals: Identify and shade the shapes of individuals impacted by DMD. This visual representation helps quickly <a href=\"https:\/\/opengenetics.pressbooks.tru.ca\/chapter\/pedigree-analysis\" rel=\"noopener noreferrer nofollow\" target=\"_blank\">identify inheritance patterns and potential carriers<\/a>.<\/li>\n<li>Review and Revise: After completing the chart, meticulously review it for accuracy. Ensure that all relationships and involved individuals are correctly depicted. Revise the chart as necessary based on additional insights or corrections provided by relatives, maintaining the integrity of the information. A well-constructed pedigree chart not only clarifies relationships but also highlights potential <a href=\"https:\/\/www.trakgene.com\/cy\/\" target=\"_blank\" rel=\"noopener\">health risks<\/a> for future generations.<\/li>\n<\/ol>\n<p><img decoding=\"async\" alt=\"Each box represents a step in the process of creating a pedigree chart. Follow the arrows to see how to move from one step to the next, ensuring you gather all necessary information and accurately depict relationships.\" src=\"https:\/\/images.tely.ai\/telyai\/ejgezgyq-each-box-represents-a-step-in-the-process-of-creating-a-pedigree-chart-follow-the-arrows-to-see-how-to-move-from-one-step-to-the-next-ensuring-you-gather-all-necessary-information-and-accurately-depict-relationships.webp\" title=\"Each box represents a step in the process of creating a pedigree chart. Follow the arrows to see how to move from one step to the next, ensuring you gather all necessary information and accurately depict relationships.\" \/><\/p>\n<h2 id=\"interpret-the-pedigree-chart-assessing-risks-and-implications\">Interpret the Pedigree Chart: Assessing Risks and Implications<\/h2>\n<ol>\n<li><strong>Identify <a href=\"https:\/\/www.trakgene.com\/cy\/\" target=\"_blank\" rel=\"noopener\">Affected Individuals<\/a><\/strong>: Identifying individuals affected by <a href=\"https:\/\/frontiersin.org\/journals\/pediatrics\/articles\/10.3389\/fped.2021.716424\/full\" rel=\"noopener noreferrer nofollow\" target=\"_blank\">Duchenne Muscular Dystrophy (DMD)<\/a> is essential for understanding its transmission within families. Begin by locating all filled shapes on the <a href=\"https:\/\/www.trakgene.com\/cy\/\" target=\"_blank\" rel=\"noopener\">pedigree of Duchenne muscular dystrophy<\/a> chart, which represent individuals affected by DMD. Understanding the pedigree of Duchenne muscular dystrophy is crucial for tracing how the disorder has been transmitted through the family.<\/li>\n<li><strong>Determine Genetic Status<\/strong>: Evaluate the <a href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC7537677\" rel=\"noopener noreferrer nofollow\" target=\"_blank\">genetic status of females<\/a> in the pedigree. If a woman has a son affected by DMD, she is likely a carrier of the trait. If she has no affected children, additional <a href=\"https:\/\/www.trakgene.com\/cy\/\" target=\"_blank\" rel=\"noopener\">genetic testing<\/a> might be required to verify her genetic status, as roughly 50% to 70% of asymptomatic females may not show increased creatine kinase (CK) levels.<\/li>\n<li><strong>Analyze <a href=\"https:\/\/www.trakgene.com\/cy\/2026\/01\/30\/understanding-duchenne-muscular-dystrophys-mode-of-inheritance\/\">Inheritance Patterns<\/a><\/strong>: Examine the inheritance patterns depicted in the chart. In DMD, <a href=\"https:\/\/www.trakgene.com\/cy\/2026\/03\/13\/understanding-pku-inheritance-definition-implications-and-history\/\">affected males<\/a> usually do not pass the pedigree of Duchenne muscular dystrophy to their sons but can convey the status of being a carrier to their daughters. This pattern is crucial for forecasting the risk for future offspring according to the pedigree of Duchenne muscular dystrophy, as heterozygous females have a 25% chance of having an affected son.<\/li>\n<li><strong>Determine Risks<\/strong>: Use the information from the pedigree of Duchenne muscular dystrophy to assess the likelihood of future children being affected or carriers. For example, if a <a href=\"https:\/\/www.trakgene.com\/cy\/2026\/02\/19\/what-is-an-inheritance-pattern-understanding-its-importance-in-genetics\/\">carrier female<\/a> has offspring with an unaffected male, there is a 50% probability for each child to be a carrier and a 25% probability for a son to be affected.<\/li>\n<li><strong>Discuss Implications<\/strong>: After examining the pedigree, discuss the consequences with the relatives. This encompasses possible <a href=\"https:\/\/rarediseaseadvisor.com\/news\/risk-assessment-tool-identify-patients-dmd-young\" rel=\"noopener noreferrer nofollow\" target=\"_blank\">health tracking for affected individuals<\/a> and choices for genetic testing for at-risk relatives. Getting a timely and accurate genetic diagnosis is key for managing DMD effectively and making informed choices about family planning.<\/li>\n<\/ol>\n<p><img decoding=\"async\" alt=\"Each box represents a step in understanding the pedigree chart. Follow the arrows to see how to move from identifying affected individuals to discussing the implications with family members.\" src=\"https:\/\/images.tely.ai\/telyai\/gubodrkg-each-box-represents-a-step-in-understanding-the-pedigree-chart-follow-the-arrows-to-see-how-to-move-from-identifying-affected-individuals-to-discussing-the-implications-with-family-members.webp\" title=\"Each box represents a step in understanding the pedigree chart. Follow the arrows to see how to move from identifying affected individuals to discussing the implications with family members.\" \/><\/p>\n<h2 id=\"utilize-digital-tools-for-enhanced-pedigree-analysis\">Utilize Digital Tools for Enhanced Pedigree Analysis<\/h2>\n<ol>\n<li>Explore Available Software: Choosing the right digital tools for the <a href=\"https:\/\/www.trakgene.com\/cy\/2026\/02\/01\/4-best-practices-for-effective-data-pedigree-management\/\">pedigree of Duchenne muscular dystrophy<\/a> analysis is crucial for enhancing <a href=\"https:\/\/www.trakgene.com\/cy\/2026\/02\/24\/4-best-practices-for-using-clinical-pedigree-software-effectively\/\">patient care<\/a> and ensuring accurate risk assessments. Investigate various digital pedigree chart makers, particularly <a href=\"https:\/\/www.trakgene.com\/cy\/\" target=\"_blank\" rel=\"noopener\">TrakGene&#8217;s Smart Pedigree Chart Maker<\/a>, which features intuitive options for creating detailed ancestral histories. This software improves the accuracy of pedigree charts, which in turn enhances patient care and outcomes.<\/li>\n<li>Integration with Health Records: Opt for tools that seamlessly integrate with <a href=\"https:\/\/www.trakgene.com\/cy\/\" target=\"_blank\" rel=\"noopener\">electronic health records<\/a> (EHRs). This integration facilitates streamlined data entry and ensures that all pertinent health information is readily accessible. The combination of EHRs with <a href=\"https:\/\/www.trakgene.com\/cy\/\" target=\"_blank\" rel=\"noopener\">pedigree analysis software<\/a> has been shown to enhance the accuracy of hereditary risk assessments, leading to improved clinical decision-making.<\/li>\n<li>Utilize Analysis Features: Select software that includes robust analysis tools for calculating risks and generating insightful reports. These features are crucial for assessing the likelihood of the pedigree of Duchenne Muscular Dystrophy (DMD) in family members, providing valuable insights that can inform counseling strategies. Advanced <a href=\"https:\/\/www.trakgene.com\/cy\/2026\/03\/09\/best-practices-for-using-pedigree-drawing-software-in-counseling\/\">pedigree analysis tools<\/a> can lead to a 30% increase in the identification of at-risk individuals compared to traditional methods.<\/li>\n<li>Training and Support: Make sure you have access to thorough training resources and customer support for the digital tools you select. Familiarizing yourself with the software not only enhances your efficiency but also improves the effectiveness of pedigree analysis. Organizations that invest in thorough training report a significant increase in patient load for genetic counselors, highlighting the importance of continuous education.<\/li>\n<li>Stay Updated: Remain informed about new developments in digital tools for genetics. The field is rapidly evolving, and advancements in software features can significantly enhance your practice. Engaging with the genetics community and participating in workshops can provide insights into best practices and emerging trends. Neglecting to stay updated on these advancements could hinder your ability to provide optimal care for patients.<\/li>\n<\/ol>\n<p><img decoding=\"async\" alt=\"Each box represents a key step in improving pedigree analysis. Follow the arrows to see how each step builds on the previous one, leading to better patient care and outcomes.\" src=\"https:\/\/images.tely.ai\/telyai\/dgwprrjp-each-box-represents-a-key-step-in-improving-pedigree-analysis-follow-the-arrows-to-see-how-each-step-builds-on-the-previous-one-leading-to-better-patient-care-and-outcomes.webp\" title=\"Each box represents a key step in improving pedigree analysis. Follow the arrows to see how each step builds on the previous one, leading to better patient care and outcomes.\" \/><\/p>\n<h2 id=\"conclusion\">Conclusion<\/h2>\n<p>Understanding Duchenne Muscular Dystrophy (DMD) is essential for families navigating its complexities and challenges. By mastering the intricacies of DMD, families can effectively address the challenges it presents, from genetic counseling to informed family planning. The insights gained from understanding DMD empower families and highlight the importance of early interventions and innovative therapies.<\/p>\n<p>Throughout this tutorial, we have explored key points, including:<\/p>\n<ol>\n<li>The significance of accurate pedigree construction<\/li>\n<li>The role of genetic counselors<\/li>\n<li>The utilization of digital tools for effective analysis<\/li>\n<\/ol>\n<p>The step-by-step guide provided practical strategies for creating and interpreting pedigree charts, which serve as vital tools for assessing genetic risks and implications within families. Furthermore, advancements in digital tools for pedigree analysis enhance the accuracy and effectiveness of genetic risk assessments, ultimately improving patient care.<\/p>\n<p>In conclusion, understanding DMD encompasses both genetic factors and the emotional challenges families endure. By engaging with genetic counseling and utilizing robust pedigree analysis, families can make informed decisions that significantly impact their future. This knowledge equips families with essential tools and information to effectively confront DMD.<\/p>\n<h2 id=\"frequently-asked-questions\">Frequently Asked Questions<\/h2>\n<p><strong>What is Duchenne Muscular Dystrophy (DMD)?<\/strong><\/p>\n<p>Duchenne Muscular Dystrophy is a genetic disorder characterized by muscle degeneration and weakness due to mutations in the dystrophin gene on the X chromosome.<\/p>\n<p><strong>Who is primarily affected by DMD?<\/strong><\/p>\n<p>DMD primarily affects boys, although females can be carriers of the mutation without showing symptoms.<\/p>\n<p><strong>How is DMD inherited?<\/strong><\/p>\n<p>DMD follows an X-linked recessive inheritance pattern, meaning that the condition is passed down through the X chromosome.<\/p>\n<p><strong>Why is understanding DMD&#8217;s inheritance patterns important?<\/strong><\/p>\n<p>Understanding the inheritance patterns of DMD is vital for genetic counseling, as it helps evaluate the risk of DMD in future generations and informs family planning.<\/p>\n<p><strong>What types of mutations are most common in the DMD gene?<\/strong><\/p>\n<p>Most mutations in the DMD gene are deletions, which can significantly influence the severity of the disorder.<\/p>\n<p><strong>What is the EXPLORE44\u00ae trial?<\/strong><\/p>\n<p>The EXPLORE44\u00ae trial demonstrated significant delivery of phosphorodiamidate morpholino oligomers (PMOs) to skeletal muscle, resulting in increased dystrophin production, which indicates potential for innovative therapies for DMD.<\/p>\n<p><strong>What role do corticosteroids play in the treatment of DMD?<\/strong><\/p>\n<p>Early interventions, such as corticosteroid treatment, can enhance motor function in patients with DMD.<\/p>\n<p><strong>How do genetic counselors assist families affected by DMD?<\/strong><\/p>\n<p>Genetic counselors help families understand carrier status, the risks for future children, and provide emotional and practical support in navigating the complexities of DMD inheritance.<\/p>\n<p><strong>What impact does understanding DMD have on families?<\/strong><\/p>\n<p>Understanding DMD informs medical decisions and profoundly affects the emotional landscape of families facing this diagnosis.<\/p>\n<h2 id=\"list-of-sources\">List of Sources<\/h2>\n<ol>\n<li>Explain Duchenne Muscular Dystrophy and Its Inheritance Patterns\n<ul>\n<li>MDA 2026: Duvyzat shows DMD benefits even at lower dose levels (https:\/\/musculardystrophynews.com\/news\/mds-2026-duvyzat-shows-dmd-benefits-even-lower-dose-levels)<\/li>\n<li>DMD Awareness Week: Duchenne Candidates to Watch in 2026 | NeurologyLive &#8211; Clinical Neurology News and Neurology Expert Insights (https:\/\/neurologylive.com\/view\/dmd-awareness-week-duchenne-candidates-watch-2026)<\/li>\n<li>Causes\/Inheritance &#8211; Duchenne Muscular Dystrophy (DMD) &#8211; Diseases | Muscular Dystrophy Association (https:\/\/mda.org\/disease\/duchenne-muscular-dystrophy\/causes-inheritance)<\/li>\n<li>FDA grants Breakthrough Therapy designation to Duchenne muscular dystrophy therapeutic | Drug Discovery News (https:\/\/drugdiscoverynews.com\/fda-grants-breakthrough-therapy-designation-to-first-in-class-aoc-therapeutic-for-duchenne-muscular-dystrophy-16530)<\/li>\n<li>News (https:\/\/parentprojectmd.org\/news)<\/li>\n<\/ul>\n<\/li>\n<li>Construct a Pedigree Chart for DMD: Step-by-Step Guide\n<ul>\n<li>4.2 Symbols used in Pedigree Charts &#8211; Introduction to Genetics (https:\/\/opengenetics.pressbooks.tru.ca\/chapter\/pedigree-analysis)<\/li>\n<li>How to Draw a Pedigree (https:\/\/humangenetics.medicine.uiowa.edu\/resources\/how-draw-pedigree)<\/li>\n<\/ul>\n<\/li>\n<li>Interpret the Pedigree Chart: Assessing Risks and Implications\n<ul>\n<li>New Risk Assessment Tool Could Identify Young Patients With DMD (https:\/\/rarediseaseadvisor.com\/news\/risk-assessment-tool-identify-patients-dmd-young)<\/li>\n<li>Quotes on Genes (https:\/\/medium.com\/@mnemko\/quotes-on-genes-64f9f457d1f)<\/li>\n<li>Frontiers | Case Report: The Genetic Diagnosis of Duchenne Muscular Dystrophy in the Middle East (https:\/\/frontiersin.org\/journals\/pediatrics\/articles\/10.3389\/fped.2021.716424\/full)<\/li>\n<li>Population-Wide Duchenne Muscular Dystrophy Carrier Detection by CK and Molecular Testing &#8211; PMC (https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC7537677)<\/li>\n<\/ul>\n<\/li>\n<li>Utilize Digital Tools for Enhanced Pedigree Analysis\n<ul>\n<li>News | TrakGene (https:\/\/trakgene.com\/en\/news)<\/li>\n<li>4 Best Practices for Genetic Pedigree Software Chart Review | TrakGene (https:\/\/trakgene.com\/2026\/04\/18\/4-best-practices-for-genetic-pedigree-software-chart-review)<\/li>\n<li>Enhance Workflow Automation with Effective Pedigree Analysis Tools | TrakGene (https:\/\/trakgene.com\/cy\/2026\/03\/08\/enhance-workflow-automation-with-effective-pedigree-analysis-tools)<\/li>\n<li>Enhance Patient Care with Pedigree Analysis Software and Family History | TrakGene (https:\/\/trakgene.com\/ms\/2026\/04\/24\/enhance-patient-care-with-pedigree-analysis-software-and-family-history)<\/li>\n<li>PEDSTATS (https:\/\/bio.tools\/pedstats)<\/li>\n<\/ul>\n<\/li>\n<\/ol>","protected":false},"excerpt":{"rendered":"<p>Introduction Duchenne Muscular Dystrophy (DMD) presents significant challenges for affected families, particularly in understanding its genetic inheritance. Grasping the genetic inheritance patterns of DMD is essential for informed medical decisions and effective family planning. Families must navigate the complexities of DMD to make informed choices for future generations, utilizing available resources and tools. By equipping [&hellip;]<\/p>\n","protected":false},"author":255,"featured_media":22649,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"content-type":"","_glsr_average":0,"_glsr_ranking":0,"_glsr_reviews":0,"footnotes":""},"categories":[183],"tags":[],"class_list":["post-22650","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-family-history-and-pedigree-analysis"],"_links":{"self":[{"href":"https:\/\/www.trakgene.com\/cy\/wp-json\/wp\/v2\/posts\/22650","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.trakgene.com\/cy\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.trakgene.com\/cy\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.trakgene.com\/cy\/wp-json\/wp\/v2\/users\/255"}],"replies":[{"embeddable":true,"href":"https:\/\/www.trakgene.com\/cy\/wp-json\/wp\/v2\/comments?post=22650"}],"version-history":[{"count":1,"href":"https:\/\/www.trakgene.com\/cy\/wp-json\/wp\/v2\/posts\/22650\/revisions"}],"predecessor-version":[{"id":22651,"href":"https:\/\/www.trakgene.com\/cy\/wp-json\/wp\/v2\/posts\/22650\/revisions\/22651"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.trakgene.com\/cy\/wp-json\/wp\/v2\/media\/22649"}],"wp:attachment":[{"href":"https:\/\/www.trakgene.com\/cy\/wp-json\/wp\/v2\/media?parent=22650"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.trakgene.com\/cy\/wp-json\/wp\/v2\/categories?post=22650"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.trakgene.com\/cy\/wp-json\/wp\/v2\/tags?post=22650"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}