{"id":2525,"date":"2026-07-16T17:17:00","date_gmt":"2026-07-16T17:17:00","guid":{"rendered":"https:\/\/genolifeadn.com\/?p=2525"},"modified":"2026-07-16T17:20:36","modified_gmt":"2026-07-16T17:20:36","slug":"la-fibrosis-quistica","status":"publish","type":"post","link":"https:\/\/genolifeadn.com\/en\/la-fibrosis-quistica\/","title":{"rendered":"\u00a0Cystic Fibrosis"},"content":{"rendered":"<div data-elementor-type=\"wp-post\" data-elementor-id=\"2525\" class=\"elementor elementor-2525\" data-elementor-settings=\"{&quot;ha_cmc_init_switcher&quot;:&quot;no&quot;}\" data-elementor-post-type=\"post\">\n\t\t\t\t\t\t<section data-particle_enable=\"false\" data-particle-mobile-disabled=\"false\" class=\"elementor-section elementor-top-section elementor-element elementor-element-15e5cefd elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"15e5cefd\" data-element_type=\"section\" data-e-type=\"section\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;,&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t\t\t<div class=\"elementor-background-overlay\"><\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-top-column elementor-element elementor-element-155aff09\" data-id=\"155aff09\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-0b62c3b elementor-widget elementor-widget-text-editor\" data-id=\"0b62c3b\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t Cystic Fibrosis\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t<div class=\"elementor-column elementor-col-50 elementor-top-column elementor-element elementor-element-1c22e56d\" data-id=\"1c22e56d\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-7074077 elementor-widget__width-initial elementor-widget elementor-widget-image\" data-id=\"7074077\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"image.default\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<img fetchpriority=\"high\" decoding=\"async\" width=\"800\" height=\"800\" src=\"https:\/\/genolifeadn.com\/wp-content\/uploads\/2026\/07\/Blog4-1024x1024.png\" class=\"attachment-large size-large wp-image-2527\" alt=\"\" srcset=\"https:\/\/genolifeadn.com\/wp-content\/uploads\/2026\/07\/Blog4-1024x1024.png 1024w, https:\/\/genolifeadn.com\/wp-content\/smush-webp\/2026\/07\/Blog4-300x300.png.webp 300w, https:\/\/genolifeadn.com\/wp-content\/smush-webp\/2026\/07\/Blog4-150x150.png.webp 150w, https:\/\/genolifeadn.com\/wp-content\/uploads\/2026\/07\/Blog4-768x768.png 768w, https:\/\/genolifeadn.com\/wp-content\/uploads\/2026\/07\/Blog4-1536x1536.png 1536w, https:\/\/genolifeadn.com\/wp-content\/smush-webp\/2026\/07\/Blog4-12x12.png.webp 12w, https:\/\/genolifeadn.com\/wp-content\/uploads\/2026\/07\/Blog4.png 2048w\" sizes=\"(max-width: 800px) 100vw, 800px\" \/>\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t<div data-particle_enable=\"false\" data-particle-mobile-disabled=\"false\" class=\"elementor-element elementor-element-921f3f5 e-flex e-con-boxed e-con e-parent\" data-id=\"921f3f5\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-02f92e7 elementor-widget-divider--view-line elementor-widget elementor-widget-divider\" data-id=\"02f92e7\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t\t\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t<\/span>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-2a74d87 elementor-widget elementor-widget-text-editor\" data-id=\"2a74d87\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p>In Mexico, there are 350 new cases of cystic fibrosis each year. The\u00a0<strong>neonatal screening<\/strong>\u00a0is a test to detect this disease before symptoms appear. However, this\u00a0<strong>It is not a confirmatory test.<\/strong>\u00a0y\u00a0<strong>It does not detect cystic fibrosis in all patients.\u00a0<\/strong>In addition, it is important to identify the specific mutation so that appropriate treatment can be determined through other molecular tests. Cystic fibrosis must be detected and treated from the first days of life, as patients without proper treatment may die during childhood or adolescence.<\/p><p>At\u00a0<strong>At Genolife, we perform various molecular tests that can help you detect the disease early.<\/strong>. Here, we'll tell you what they are and help you decide which one to choose.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div data-particle_enable=\"false\" data-particle-mobile-disabled=\"false\" class=\"elementor-element elementor-element-d929ac2 e-flex e-con-boxed e-con e-parent\" data-id=\"d929ac2\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-03d0f16 elementor-widget-divider--view-line elementor-widget elementor-widget-divider\" data-id=\"03d0f16\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t\t\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t<\/span>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-efa5ba6 elementor-widget elementor-widget-text-editor\" data-id=\"efa5ba6\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\tWhat Is Cystic Fibrosis?\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-948e3af elementor-widget elementor-widget-text-editor\" data-id=\"948e3af\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p>Cystic fibrosis (CF) is an autosomal recessive disorder that occurs in approximately 1 in 3,500 births. Most patients become symptomatic at birth or shortly after birth; respiratory infections and poor weight gain are the most common symptoms.<br \/>Cystic fibrosis is a multisystemic disease that affects the epithelium of the respiratory tract, the pancreas, the intestine, the hepatobiliary system, and the exocrine sweat glands. Complications arising from cystic fibrosis include progressive obstructive lung disease with bronchiectasis, frequent hospitalizations due to lung disease, pancreatic insufficiency and malnutrition, recurrent sinusitis and bronchitis, and male infertility. Lung disease is the leading cause of morbidity and mortality in cystic fibrosis.<br \/>In recent years, there have been notable improvements in the health of people with cystic fibrosis, and life expectancy has increased substantially; however, this disease continues to limit the survival and quality of life of those who have it.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div data-particle_enable=\"false\" data-particle-mobile-disabled=\"false\" class=\"elementor-element elementor-element-38514bd e-flex e-con-boxed e-con e-parent\" data-id=\"38514bd\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-5d35499 elementor-widget-divider--view-line elementor-widget elementor-widget-divider\" data-id=\"5d35499\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t\t\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t<\/span>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-7706322 elementor-widget elementor-widget-text-editor\" data-id=\"7706322\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\tSymptoms and signs that may be observed in children and young adults include:\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-bd7aa72 elementor-widget elementor-widget-text-editor\" data-id=\"bd7aa72\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<ul><li><em>A salty taste on the skin; their sweat may contain two to five times as much salt<\/em><\/li><li><em>Intestinal Obstruction<\/em><\/li><li><em>Pancreatic insufficiency that usually manifests in early life and may be progressive<\/em><\/li><li><em>Thick mucus<\/em><\/li><li><em>Chronic or wheezing cough<\/em><\/li><li><em>Frequent respiratory infections leading to pneumonia and bronchitis<\/em><\/li><li><em>Nasal Polyps and Chronic Sinusitis<\/em><\/li><li><em>Inflammation and Obstruction of the Bile Ducts<\/em><\/li><li><em>Protrusion of one part of the intestine into another<\/em><\/li><li><em>Adolescents may experience growth retardation, delayed onset of puberty, and reduced exercise tolerance<\/em><\/li><li><em>Risk of Dehydration During Episodes of Fever Due to Excessive Sweating<\/em><\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div data-particle_enable=\"false\" data-particle-mobile-disabled=\"false\" class=\"elementor-element elementor-element-ffbb0db e-flex e-con-boxed e-con e-parent\" data-id=\"ffbb0db\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-c5f7858 elementor-widget-divider--view-line elementor-widget elementor-widget-divider\" data-id=\"c5f7858\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t\t\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t<\/span>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-064db87 elementor-widget elementor-widget-text-editor\" data-id=\"064db87\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\tWhat causes this disease?\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-b976b4f elementor-widget elementor-widget-text-editor\" data-id=\"b976b4f\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p>Since 1989, we have known that cystic fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which encodes the CFTR protein. This anion channel, which conducts chloride and bicarbonate across the apical membrane of various epithelial cells, regulates the transport of water and ions and maintains the hydration of the epithelial surface.<\/p><p>The release of bicarbonate in the airways is important for the proper development of mucins and for defense against bacteria. In the intestine, bicarbonate release is necessary to buffer gastric acidity and allow for the activation of pancreatic enzymes. To date, more than\u00a0<strong>2,000 mutations<\/strong>\u00a0different from\u00a0<strong>CFTR<\/strong>\u00a0y\u00a0<strong>F508del<\/strong>\u00a0It is, by far, the most common.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div data-particle_enable=\"false\" data-particle-mobile-disabled=\"false\" class=\"elementor-element elementor-element-92b5c46 e-flex e-con-boxed e-con e-parent\" data-id=\"92b5c46\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-cbc3060 elementor-widget-divider--view-line elementor-widget elementor-widget-divider\" data-id=\"cbc3060\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t\t\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t<\/span>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-fc6e074 elementor-widget elementor-widget-text-editor\" data-id=\"fc6e074\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\tDiagnosis of the disease\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-06bb946 elementor-widget elementor-widget-text-editor\" data-id=\"06bb946\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><strong>Neonatal screening and chlorine in sweat<\/strong><br \/>Cystic fibrosis is now recognized as a major genetic disease worldwide. Diagnosis is primarily made through the\u00a0<strong>Neonatal Cystic Fibrosis Screening.<\/strong><br \/>The neonatal screening test for cystic fibrosis detects elevated levels of immunoreactive trypsinogen (IRT) in the newborn's blood. It is not a diagnostic test; therefore, a positive result requires confirmation with diagnostic tests:\u00a0<strong>Chlorine in sweat or molecular analysis.<\/strong><br \/>It's still important to be aware of FQ, because the<strong>\u00a0Neonatal screening does not detect cystic fibrosis in all patients<\/strong>\u00a0and it is possible that the disease may not manifest until adulthood. In addition, a molecular analysis is essential, since identifying the patient\u2019s CFTR mutations paves the way for personalized therapy.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div data-particle_enable=\"false\" data-particle-mobile-disabled=\"false\" class=\"elementor-element elementor-element-db5992e e-flex e-con-boxed e-con e-parent\" data-id=\"db5992e\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-0b1c9a7 elementor-widget-divider--view-line elementor-widget elementor-widget-divider\" data-id=\"0b1c9a7\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t\t\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t<\/span>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-b05022c elementor-widget elementor-widget-text-editor\" data-id=\"b05022c\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\tMolecular tests\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-47ac0bf elementor-widget elementor-widget-text-editor\" data-id=\"47ac0bf\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p>The discovery of the cystic fibrosis regulator gene (CFTR) has transformed the lives of patients with cystic fibrosis by leading to a treatment that can prevent serious complications if started early in childhood or as soon as possible after diagnosis.<br \/>At\u00a0<strong>Genolife<\/strong>\u00a0We offer the following tests to aid in the timely diagnosis of cystic fibrosis in patients who have the disease or in patients suspected of being carriers of the related gene:<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div data-particle_enable=\"false\" data-particle-mobile-disabled=\"false\" class=\"elementor-element elementor-element-1782ece e-flex e-con-boxed e-con e-parent\" data-id=\"1782ece\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-6670454 elementor-widget-divider--view-line elementor-widget elementor-widget-divider\" data-id=\"6670454\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t\t\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t<\/span>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-4cf55e7 elementor-widget elementor-widget-text-editor\" data-id=\"4cf55e7\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\tSingle-gene test (detection of point mutations)\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-cf6cf3c elementor-widget elementor-widget-text-editor\" data-id=\"cf6cf3c\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p>This test is primarily used to diagnose cystic fibrosis through a targeted analysis for pathogenic CFTR variants.<br \/><strong>Note:<\/strong><br \/>-The panel recommended by the American College of Medical Genetics includes the 23 pathogenic variants and has a detection rate of 97% in Eastern European Jews, 88.3% in non-Hispanic whites, 69.1% in African Americans, and 57.1% in Hispanic Americans; the detection rate in Asian Americans is unknown.<br \/>-A panel that includes more than 129 pathogenic variants would detect approximately 96% of the pathogenic variants in affected individuals.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div data-particle_enable=\"false\" data-particle-mobile-disabled=\"false\" class=\"elementor-element elementor-element-59213f3 e-flex e-con-boxed e-con e-parent\" data-id=\"59213f3\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-fc8a68d elementor-widget-divider--view-line elementor-widget elementor-widget-divider\" data-id=\"fc8a68d\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t\t\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t<\/span>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-657f1b8 elementor-widget elementor-widget-text-editor\" data-id=\"657f1b8\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\tFull Sequencing of the CFTR Gene Using NGS\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-277e217 elementor-widget elementor-widget-text-editor\" data-id=\"277e217\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p>CFTR sequence analysis, followed by a gene-specific deletion\/duplication analysis, is performed if only one pathogenic variant is found or if none are found.<br \/><strong>Note:<\/strong><br \/>It is the initial diagnostic test for:<br \/>-Individuals from an ethnic group for whom the sensitivity of the targeted analysis is low.<br \/>-Prenatal testing for a high-risk fetus.<br \/>-Prenatal testing in a low-risk fetus with an echogenic bowel identified on a prenatal ultrasound.<br \/>-A baby with an elevated IRT test result in the newborn screening and a sweat chloride level of 30\u201359 mEq\/L (intermediate result).<br \/>-A symptomatic infant (e.g., an infant with meconium ileus) who is too young to produce adequate amounts of sweat.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div data-particle_enable=\"false\" data-particle-mobile-disabled=\"false\" class=\"elementor-element elementor-element-0ce083f e-flex e-con-boxed e-con e-parent\" data-id=\"0ce083f\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-f5d33e7 elementor-widget-divider--view-line elementor-widget elementor-widget-divider\" data-id=\"f5d33e7\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t\t\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t<\/span>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-00c7eff elementor-widget elementor-widget-text-editor\" data-id=\"00c7eff\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\tMultigene panel\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-b45d028 elementor-widget elementor-widget-text-editor\" data-id=\"b45d028\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><a href=\"https:\/\/genolifeadn.com\/en\/secuenciacion-del-exoma\/\">Exome sequencing<\/a>\u00a0allows us to identify which mutations are present throughout the genome. It is a\u00a0<strong>powerful tool<\/strong>\u00a0which allows us to analyze our\u00a0<strong>genetic code<\/strong>\u00a0since its goal is to obtain as much genetic information as possible from a patient, by searching for genetic variants throughout the approximately\u00a0<strong>20,000 genes<\/strong>\u00a0that make it up.<br \/>One of the greatest advantages of this technique is that it helps us accurately detect any genetic abnormalities that could have a direct impact on our quality of life.<br \/>Although it is more expensive, it provides us with much more information than the previous tests, as it allows for the detection of variants related to this disease and others. Sometimes it is more costly to undergo individual tests to obtain an accurate diagnosis of the disease, and this test can spare us from the infamous diagnostic odyssey.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div data-particle_enable=\"false\" data-particle-mobile-disabled=\"false\" class=\"elementor-element elementor-element-1dfcabd e-flex e-con-boxed e-con e-parent\" data-id=\"1dfcabd\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-a875cbb elementor-widget-divider--view-line elementor-widget elementor-widget-divider\" data-id=\"a875cbb\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t\t\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t<\/span>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-07da3d6 elementor-widget elementor-widget-text-editor\" data-id=\"07da3d6\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\tKey Points\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-34baff3 elementor-widget elementor-widget-text-editor\" data-id=\"34baff3\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<ul><li>Improved molecular genetic testing has made it possible to diagnose cystic fibrosis, as well as to identify individuals with nonclassical presentations of cystic fibrosis and related disorders.<\/li><li>Identifying the mutations in the CFTR gene associated with disease manifestations is a priority for guiding decisions regarding patient follow-up and treatment.<\/li><li>There is no definitive cure for cystic fibrosis; however, the FDA has approved medications that consist of a combination of compounds that, on the one hand, increase the amount of CFTR protein on the cell surface and, on the other hand, enhance the protein\u2019s function. The use of drugs has also been approved for certain mutations in the CFTR gene that cause cystic fibrosis.<\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div data-particle_enable=\"false\" data-particle-mobile-disabled=\"false\" class=\"elementor-element elementor-element-205ca06 e-flex e-con-boxed e-con e-parent\" data-id=\"205ca06\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;,&quot;_ha_eqh_enable&quot;:false}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t<div data-particle_enable=\"false\" data-particle-mobile-disabled=\"false\" class=\"elementor-element elementor-element-5f08ce9 e-con-full e-flex e-con e-child\" data-id=\"5f08ce9\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;,&quot;_ha_eqh_enable&quot;:false}\">\n\t\t<div data-particle_enable=\"false\" 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class=\"hm hm-phone\"><\/i><\/span>                    \n                    <span class=\"cretive-button-text\">Phone<\/span>\n\n                                    <\/div>\n\t                        <\/a>\n        <\/div>\n        \t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>","protected":false},"excerpt":{"rendered":"<p>la Fibrosis Qu\u00edstica En M\u00e9xico cada a\u00f1o se presentan 350 nuevos casos de fibrosis qu\u00edstica. El\u00a0tamiz neonatal\u00a0es una prueba para detectar esta enfermedad antes de que se presenten los s\u00edntomas. Sin embargo, esta\u00a0no es una prueba confirmatoria\u00a0y\u00a0no detecta la fibrosis qu\u00edstica en todos los pacientes.\u00a0Adem\u00e1s, de que es importante conocer que mutaci\u00f3n es la que [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":2527,"comment_status":"open","ping_status":"open","sticky":false,"template":"elementor_header_footer","format":"standard","meta":{"_joinchat":[],"footnotes":""},"categories":[1],"tags":[],"class_list":["post-2525","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-sin-categoria"],"_links":{"self":[{"href":"https:\/\/genolifeadn.com\/en\/wp-json\/wp\/v2\/posts\/2525","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/genolifeadn.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/genolifeadn.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/genolifeadn.com\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/genolifeadn.com\/en\/wp-json\/wp\/v2\/comments?post=2525"}],"version-history":[{"count":4,"href":"https:\/\/genolifeadn.com\/en\/wp-json\/wp\/v2\/posts\/2525\/revisions"}],"predecessor-version":[{"id":2530,"href":"https:\/\/genolifeadn.com\/en\/wp-json\/wp\/v2\/posts\/2525\/revisions\/2530"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/genolifeadn.com\/en\/wp-json\/wp\/v2\/media\/2527"}],"wp:attachment":[{"href":"https:\/\/genolifeadn.com\/en\/wp-json\/wp\/v2\/media?parent=2525"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/genolifeadn.com\/en\/wp-json\/wp\/v2\/categories?post=2525"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/genolifeadn.com\/en\/wp-json\/wp\/v2\/tags?post=2525"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}