Zobrazeno 1 - 10
of 80
pro vyhledávání: '"Mehnaz Atiq"'
Publikováno v:
Journal of the Pakistan Medical Association, Vol 73, Iss 05 (2023)
One of the rare diseases with a high mortality rate in infants is congenital heart block (CHB) with neonatal lupus erythematosus (NLE) as the most common cause. A permanent pacemaker (PPM) is indicated for symptomatic bradycardia. The choice of PPM i
Externí odkaz:
https://doaj.org/article/e22d2d9fa5dc460b87291474234a0c0f
Publikováno v:
Journal of the Pakistan Medical Association, Vol 72, Iss 9 (2022)
Cardiac rhabdomyoma is the most common primary cardiac tumour and is considered to be a hamartoma of developing embryonic cardiac myocytes. It is commonly seen in tuberous sclerosis. The size and location of the tumour is the surrogate determinant of
Externí odkaz:
https://doaj.org/article/401de8ec48b5493fb77cb42d88bd03e7
Publikováno v:
Monaldi Archives for Chest Disease (2022)
Anomalous left coronary artery from pulmonary artery (ALCAPA), also known as Bland-White-Garland syndrome, is a rare cardiac disease. This condition may present with complications such as myocardial infarction, left ventricular dilatation, mitral reg
Externí odkaz:
https://doaj.org/article/c1701d3f5d034bd5b108f74752f72856
Autor:
Mehnaz Atiq
Publikováno v:
Liaquat National Journal of Primary Care, Vol 2, Iss 1, Pp 39-42 (2020)
Congenital heart disease has an overall incidence of 8-10/1000 live births and is similar across the globe. The incidence may be higher in countries where consanguinity is high, suggesting an autosomal recessive gene as a risk factor. Advances in su
Externí odkaz:
https://doaj.org/article/9199845864b24d04890de68390878436
Publikováno v:
Journal of the Saudi Heart Association, Vol 29, Iss 2, Pp 139-142 (2017)
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is seldom recognized clinically in infancy or under the age of 10. We report a case of a 9-year-old girl with ARVC, who presented with signs and symptoms of heart failure and palpitations. Holter
Externí odkaz:
https://doaj.org/article/867bf5cde7a84b0497b10669707350e6
Publikováno v:
Annals of Pediatric Cardiology, Vol 5, Iss 2, Pp 129-132 (2012)
Introduction: Coronary artery involvement is the most dreaded long-term complication of Kawasaki disease. Our aim was to look at the pattern of cardiovascular involvement in Pakistani children admitted with Kawasaki disease. Methods: This study inclu
Externí odkaz:
https://doaj.org/article/2a725f3c976f4fe5a3b569fffe20a380
Autor:
Faheem Ul Haq, Fatima Jalil, Saman Hashmi, Maliha Iqbal Jumani, Aamer Imdad, Mehnaz Jabeen, Javad Tauseef Hashmi, Furqan Bin Irfan, Muhammad Imran, Mehnaz Atiq
Publikováno v:
Annals of Pediatric Cardiology, Vol 4, Iss 2, Pp 117-121 (2011)
Introduction: Congenital heart disease (CHD) is associated with multiple risk factors, consanguinity may be one such significant factor. The role of consanguinity in the etiology of CHD is supported by inbreeding studies, which demonstrate an autosom
Externí odkaz:
https://doaj.org/article/8b647babc5954b388e66d889201b3ab6
Publikováno v:
Journal of the Pakistan Medical Association. 73:1113-1116
One of the rare diseases with a high mortality rate in infants is congenital heart block (CHB) with neonatal lupus erythematosus (NLE) as the most common cause. A permanent pacemaker (PPM) is indicated for symptomatic bradycardia. The choice of PPM i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fbc38dbea3b6f2ad194827ed24fa1b8
https://doi.org/10.47391/jpma.6674
https://doi.org/10.47391/jpma.6674
Publikováno v:
Journal of the College of Physicians and Surgeons Pakistan. 31:S135-S137
Kawasaki disease (KD) is a systemic vasculitis of unknown cause affecting children under 5 years of age. It is thought to be triggered by several viruses. Recently, Kawasaki-like disease has been reported worldwide in patients with COVID-19, giving r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34eb5e1a0ca09bf622008a49e18b45a2
https://doi.org/10.29271/jcpsp.2021.supp2.s135
https://doi.org/10.29271/jcpsp.2021.supp2.s135
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.