5 results match your criteria: "Madina Maternity and Children Hospital[Affiliation]"

NPHP3 splice acceptor site variant is associated with infantile nephronophthisis and asphyxiating thoracic dystrophy; A rare combination.

Eur J Med Genet

October 2022

Department of Biochemistry, College of Medicine & Center for Genetics and Inherited Diseases, Taibah University Medina, Saudi Arabia. Electronic address:

Nephronophthisis (NPHP) is a group of rare inherited ciliopathy disorders characterized by the multicystic dysplastic kidney, oligohydramnios, and tubulointerstitial nephritis that progresses to end-stage renal disease (ESRD). NPHP is a clinically and genetically heterogeneous disorder with extrarenal symptoms including skeletal deformities, nervous system anomalies, and ophthalmologic features. Three clinical subtypes, infantile, juvenile, and adolescent, have been recognized based on age of onset of ESRD.

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Introduction: Emicizumab is a bispecific monoclonal antibody with the ability to bridge FIXa and FX, mimic FVIII, and restore normal hemostasis in patients with hemophilia A. Moreover, substantial evidence has shown that emicizumab-treated patients do not require monitoring, except before surgery or invasive procedures. However, introducing this novel drug to the market poses some challenges to physicians and clinical laboratories due to its interaction with conventional coagulation tests.

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Background: Women with gestational diabetes mellitus (GDM) are required to control their blood glucose shortly after GDM diagnosis to minimize adverse pregnancy outcomes. A real time-continuous glucose monitoring system (RT-CGMS) provides the patient with continuous information about the alterations in levels of the blood glucose. This visibility may empower the patient to modify her lifestyle and engage in therapeutic management.

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Article Synopsis
  • The study highlights the significant issue of pediatric heart disease in Madina, revealing that a substantial percentage of new cases involve congenital heart defects (CHD).
  • Over the study period, nearly 40% of new pediatric patients were diagnosed with some form of heart disease, with ventricular septal defect being the most common type of CHD.
  • The conclusion underscores the urgent need for a specialized cardiac center in Madina to facilitate timely access to care and reduce the challenges associated with transporting patients to distant facilities.
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Posterior mediastinal gastoenteric cyst in neonate.

Saudi Med J

July 2004

Department of Pediatrics and Neonatology, Madina Maternity and Children Hospital, Madina Al-Munawara, Kingdom of Saudi Arabia.

Posterior mediastinal enteric cysts are infrequently reported. They are mostly asymptomatic 1. The incidence of gastroenteric cysts presenting during immediate neonatal period is rare.

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