Cargando…

Implantation of cardiac defibrillator in an infant with hypertrophic cardiomyopathy and newly identified MYBP3 mutation

Hypertrophic cardiomyopathy has the highest incidence rate among genetically inherited cardiac diseases. It develops as a result of mutations in genes in related to the sarcomere protein in cardiac muscle. Generally, this results in asymmetrical hypertrophy. Patients who are symptomatic and have a s...

Descripción completa

Detalles Bibliográficos
Autores principales:	Güvenç, Osman, Karaer, Kadri, Haydin, Sertaç, Güzeltaş, Alper, Ergül, Yakup
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Kare Publishing 2020
Materias:	Case Report / Olgu Sunumu
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536448/ https://www.ncbi.nlm.nih.gov/pubmed/33061760 http://dx.doi.org/10.14744/TurkPediatriArs.2018.35556

Ejemplares similares

Renal mycetomas in a 10-month-old female infant without immunodeficiency
por: Gkampeta, Anastasia, et al.
Publicado: (2020)

Recurrent infections, neurologic signs, low serum uric acid levels, and lymphopenia in childhood: Purine nucleoside phosphorylase deficiency, an emergency for infants
por: Kütükçüler, Necil, et al.
Publicado: (2020)

Eosinophilic gastroenteritis as a cause of gastrointestinal tract bleeding and protein-losing enteropathy
por: Eren, Makbule, et al.
Publicado: (2020)

A case of classic galactosemia manifesting as neonatal early and profound indirect hyperbilirubinemia
por: Kavehmanesh, Zohreh, et al.
Publicado: (2020)

Alpha-lipoic acid intoxication in an adolescent girl: Case report and review of the literature
por: Polat, Sinem, et al.
Publicado: (2020)

Clinical characteristics of a Turkish family with congenital erythrocytosis due to an EPOR mutation: Is routine phlebotomy indicated in children and adolescents?
por: Sarper, Nazan, et al.
Publicado: (2020)

Acquired lung cysts in a premature neonate with congenital cytomegalovirus infection
por: Özdemir, Özmert M. A., et al.
Publicado: (2020)

Successful outcome of mucormycosis in a child with acute lymphoblastic leukemia
por: Kebudi, Rejin, et al.
Publicado: (2020)

IgG4 related disease in a seven year old girl with multiple organ involvement: A rare presentation
por: Akkelle, Bilge Şahin, et al.
Publicado: (2020)

A novel de novo mutation at the ABCC8 gene in a newborn with transient diabetes mellitus
por: Bolu, Semih, et al.
Publicado: (2020)

Primary ovarian rhabdomyosarcoma coexisting with Pseudo-Meigs’ syndrome in a young patient: a case report and brief literature review
por: Gökçe, Şule, et al.
Publicado: (2020)

A rare cause of acute severe upper airway obstruction that required endotracheal intubation: adenoid hypertrophy
por: Yıldırım, Uğur, et al.
Publicado: (2020)

The clinical characteristics of fascioliasis in pediatric patients
por: Bayhan, Gülsüm İclal, et al.
Publicado: (2020)

SLC26A3 mutation in Turkish neonate and her sibling with congenital chloride diarrhea
por: Doğan, Erkan, et al.
Publicado: (2020)

An overlooked case of a treatable hyperinsulinemic hypoglycemia: congenital glycosylation defect Type Ib
por: Haznedar, Pınar, et al.
Publicado: (2020)

A case of Type 1 Dent disease presenting with isolated persistent proteinuria
por: Güngör, Tülin, et al.
Publicado: (2020)

A first case report of neonatal persistent pneumothorax treated with an autologous blood patch
por: Huseynov, Mirzaman
Publicado: (2020)

A rare case in childhood: Pott’s puffy tumor developing secondary to frontal sinus osteoma
por: Öztürk, Necmiye, et al.
Publicado: (2020)

Gastrointestinal sarcoidosis presenting with malabsorption at an early age
por: Şengül, Özlem Kalaycık, et al.
Publicado: (2020)

The clinical and radiological course of bronchopulmonary dysplasia in twins treated with mesenchymal stem cells and followed up using lung ultrasonography
por: Öktem, Ahmet, et al.
Publicado: (2020)

The first Turkish family with Rotor syndrome diagnosed at the molecular level
por: Gümüş, Evren, et al.
Publicado: (2020)

Autoimmune rhomboencephalitis: A pediatric case report
por: Marino, Achille, et al.
Publicado: (2020)

A family with novel homozygous deletion mutation (c.1255delT; p.Phe419Serfs*12) in the glucokinase gene, which is a rare cause of permanent neonatal diabetes mellitus
por: Bolu, Semih, et al.
Publicado: (2020)

Depresyon Tanılı Bir Hastada Fonksiyonel Sağlık Örüntüleri Modeli Temelinde Bir Bakım Planı
por: Temel, Münire, et al.
Publicado: (2019)

A rare association with suffered cardiac arrest, long QT interval, and syndactyly: Timothy syndrome (LQT-8)
por: Ergül, Yakup, et al.
Publicado: (2016)

The Evaluation of Nosocomial Infections in Pediatric Patients with Extracorporeal Membrane Oxygenation Support
por: Ayyıldız, Pelin, et al.
Publicado: (2017)

Clinical and genetic characteristics and course of congenital long QT syndrome in children: A nine-year single-center experience
por: Ergül, Yakup, et al.
Publicado: (2021)

Clinical Characteristics and Mid-term Follow-up in Children with Isolated Complete Atrioventricular Block
por: Sülü, Ayşe, et al.
Publicado: (2023)

Early postoperative arrhythmias in patients undergoing congenital heart surgery
por: Öztürk, Erkut, et al.
Publicado: (2021)

Short QT syndrome in a 14-year-old patient: The first pediatric case from Turkey
por: Ergül, Yakup, et al.
Publicado: (2015)

Hybrid transcatheter pulmonary valve implantation: The first case series from Turkey
por: Güzeltaş, Alper, et al.
Publicado: (2018)

Implantable cardioverter–defibrillator in hypertrophic cardiomyopathy
por: Sanchez, Diego Jimenez, et al.
Publicado: (2018)

Living with hypertrophic cardiomyopathy and an implantable defibrillator
por: Magnusson, Peter, et al.
Publicado: (2017)

Hybrid stenting of restrictive atrial septum in an infant with hypoplastic left heart syndrome after hybrid stage 1 palliation
por: Güzeltaş, Alper, et al.
Publicado: (2015)

Catheter ablation of manifest posteroseptal accessory pathway associated with coronary sinus diverticula in a child with congenitally corrected transposition of the great arteries
por: Ergül, Yakup, et al.
Publicado: (2018)

Anesthesia in a Child with Newly Diagnosed Hypertrophic Cardiomyopathy for Placement of Implantable Cardioverter Defibrillator
por: Kumar, Rajnish, et al.
Publicado: (2018)

Valve-sparing aortic root replacement in Loeys-Dietz syndrome and a novel mutation in TGFBR2
por: Kasar, Taner, et al.
Publicado: (2018)

Electrophysiologic characteristics and catheter ablation results of tachycardia-induced cardiomyopathy in children with structurally normal heart
por: Kafalı, Hasan Candaş, et al.
Publicado: (2020)

Role of Implantable Cardioverter Defibrillators in the Treatment of Hypertrophic Cardiomyopathy
por: Ghosh, Joydeep, et al.
Publicado: (2005)

Late Arterial Switch Surgery Under ECMO Support in a Patient with Transposition of the Great Arteries with Intact Ventricular Septum: a Case Report
por: Haydin, Sertac, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_tt8b4l6gpq5kts30fjklmi4664