Manal Mustafa | Speaker | Healthcare | Pediatric Conferences 2025

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Pediatrics and Healthcare </h1> </div> </div> <div class="col-md-12 mb-2"> <p class="text-left theme-content"> <i class="fa fa-bullhorn pr-2"></i> <b>Theme:</b> Empowering the Future: Innovations in Pediatric Care and Health </p> </div> <div class="col-md-12 mb-2"> <p class="h6-text"> <span class="text-white p-2 rounded mr-2 mb-2"><i class="fa fa-calendar pr-2" aria-hidden="true"></i> May 15-16, 2025 </span> <span class="text-white p-2 rounded mr-2 mb-2"><i class="fa fa-map-marker pr-2" aria-hidden="true"></i> Dubai, UAE </span> <span class="text-white p-2 rounded mr-2 mb-2"><i class="fa fa-hotel pr-2" aria-hidden="true"></i> City Seasons Hotel Dubai </span> </p> </div> </div> </div> </div> <div class="col-md-4 my-auto"> <div class="row"> <a href="https://www.pediatric.scientexconference.com/brochure" class="col-sm-12 col-md-12 col-lg-12 col-xl-6 mb-3 text-center"> <button class="banner-btn-link py-3"><i class="fa fa-download"></i> Download Brochure</button> </a> <a 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Jalila Children鈥檚 Hospital, UAE</span> <h3 class="webcolor">Presentation Title: </h3> <h3 style="text-transform: unset;"> Six-year follow-up of a child with familial chylomicronemia syndrome: disease course and effective ness of gemfibrozil treatment case report and literature review</h3> <h3 class="webcolor">Abstract</h3> <p><div><div style="text-align: justify;"><b>Background:</b> Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disease affecting lipoprotein metabolism. The condition is characterized by hypertriglyceridemia, which may predispose patients to acute pancreatitis. FCS is estimated to occur in 1 in 1 - 2 million individuals [1] and can be diagnosed at any age, affecting all genders, races, and ethnicities equally [2].<br><br><o:p></o:p></div> <div style="text-align: justify;"><span><b>Case Presentation:</b></span><span> Here, we presented the case of a now seven years old girl with FCS on Gemfibrozil and dietary restrictions. The patient initially presented at 40 days of age with bloody diarrhea. Serum samples showed lipemia with markedly elevated triglyceride levels. She was diagnosed with FCS, confirmed by genetic testing, revealing a homozygous variant c.833C>T(p,Ser278Phe) for the LPL gene. Despite starting a low-fat diet with medium chain triglycerides (MCT) based milk formulas, the patient developed acute pancreatitis two months later, with continued elevated triglyceride levels. She was started on Gemfibrozil and fat-soluble vitamins at two months of age, with marked improvements noted during six years of treatment and follow-up (Table 1). Currently, she is well, with normal growth parameters and no other episodes of acute pancreatitis. Her triglyceride levels have maintained within normal levels (Table 1) (Fig.1).<br><br><o:p></o:p></span></div> <div style="text-align: justify;"><span><b>Conclusion:</b></span><span>Familial chylomicronemia syndrome is a rare, inherited lipid disorder that often goes underdiagnosed and unmanaged. It is mainly present in childhood but can be seen in infancy, with different manifestations. There are insufficient data regarding its treatment protocol. The mainstay of treatment is a dietary restriction, although some patients may require lipid-lowering agents. It is worth considering the Fibrate derivative (Gemfibrozil) to be one of the lines of management early after diagnosis.<o:p></o:p></span></div> <div style="text-align: justify;"><span><b>Keywords:</b></span><span> Hypertriglyceridemia; Familial Chylomicronemia Syndrome; Gemfibrozil<o:p></o:p></span></div></div></p> <h3 class="webcolor">Biography</h3> <p><div>TBA</div> </p> </div> </div> </div> </div> </div> </div> <style> </style> <div class="footer-area bg-footer parallax ptb"> <div class="container"> <div class="row f-content"> <div class="col-sm-6 col-md-6 col-lg-5"> <img src="https://www.pediatric.scientexconference.com/frontfiles/assets/img/logo.png" alt="Scientex Conference Logo" class="footer-logo"/> <div class="location-div"> <h4>Organization Location</h4> <p>1309 Coffeen Avenue, STE 1200, Sheridan, Wyoming 82801, USA</p>  </div> </div> <div class="col-sm-6 col-md-6 col-lg-4"> <div class="contact-info"> <h4 class=" footer-heading"><strong>Mail us at</strong></h4> <p>Program Enquiry<br> <a href="mailto:pediatrics@scientexevents.com">pediatrics@scientexevents.com</a> </p> <p>General Enquiry<br> <a href="mailto:contact@scientexconferences.com">contact@scientexconferences.com</a></p> <p>Registration Enquiry<br> <a href="mailto:finance@scientexconferences.com">finance@scientexconferences.com</a> <br> <a href="mailto:pediatric@scientexconference.org">pediatric@scientexconference.org</a> </p> </div> </div> <div class="col-sm-6 col-md-6 col-lg-3"> <h4>Our Social Presence</h4> <div class="f-social"> <ul> <li><a href="https://www.facebook.com/profile.php?id=61551944643525" target="_blank"><i class="fa fa-facebook-square"></i></a></li> <li><a href="https://twitter.com/rhea__vincent" target="_blank"><i class="fa fa-twitter-square"></i></a></li> <li><a href="https://www.linkedin.com/in/rhea-vincent-17240a252/" target="_blank"><i class="fa fa-linkedin-square"></i></a></li> <li><a href="https://www.youtube.com/@scientexevents" target="_blank"><i class="fa fa-youtube-square"></i></a></li></a></li> </ul> </div> <h4>Call us at</h4> <p class="mt-2"><i class="fa fa-phone"></i> USA :(+1) 716 647 2613</p> </div>  </div> </div> </div> <div class="footer-bottom"> <div class="container"> <div class="row py-3 "> <div class="col-sm-4 inner-content"> <div class="copyright m-3"> <p>漏 2024 Scientex Conferences. 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Manal Mustafa | Speaker | Healthcare | Pediatric Conferences 2025