Results 31 to 40 of about 15,555 (263)

Multimodality imaging of cor triatriatum dexter complicated with hypertrophic cardiomyopathy of restrictive phenotype

Radiology Case Reports, 2022
Cor triatriatum dexter (CTD) is an extremely rare congenital cardiac malformation in which a membrane divides the right atrium into 2 chambers. Hypertrophic cardiomyopathy (HCM) with restrictive phenotype is also a rare cardiomyopathy.
Li Liang, Min-Jie Lu, PhD
doaj   +1 more source

Left Bundle Pacing for Left Bundle Branch Block and Intermittent Third-Degree Atrioventricular Block in a MYH7 Mutation-Related Hypertrophic Cardiomyopathy With Restrictive Phenotype in a Child

Frontiers in Pediatrics, 2020
Hypertrophic cardiomyopathy (HCM) is a group of myocardial diseases defined by cardiac hypertrophy which cannot be explained by secondary causes with a non-dilated left ventricle and preserved or increased ejection fraction.
Luyan Zhang, Xueying Cheng, Jinlong Chen, Ming Zhou, Tianwei Qian, Zhongman Zhang, Jie Yin, Han Zhang, Genyin Dai, Yuming Qin, Shiwei Yang   +10 more
doaj   +1 more source

Desmin-related restrictive cardiomyopathy in a pediatric patient: A case report

Indian Journal of Pathology and Microbiology, 2013
Restrictive cardiomyopathies in the pediatric population have diverse etiologies, including storage diseases like hemosiderosis, glycogenoses and desmin with its associated proteins.
Shruti Sharma, Rajnish Juneja, Gautam Sharma, Sudheer Arava, Ruma Ray   +4 more
doaj   +1 more source

Restrictive Cardiomyopathy: A Rare Case Report [PDF]

Al Ameen Journal of Medical Sciences, 2011
We report a 28 years old male presenting with heart failure. A thorough clinical evaluation directed us towards restrictive heart disease. Doppler echocardiographic study was used as a main modality of diagnosis and cardiac catheterization confirmed the ...
Bilal Bin Abdullah*, Mehboob.M.Kalburgi, Sahana Shetty and Satyasrinivas
doaj  

Restrictive Cardiomyopathy in a Child

Pediatrics and Neonatology, 2008
Restrictive cardiomyopathy in young children is rare and carries a poor prognosis. We report an 18-month-old girl with poor feeding and abdominal distension. Except for hepatomegaly, no other gastrointestinal abnormalities were found. She had normalsized
Shan-Miao Lin, Haw-Kwei Hwang, Ming-Ren Chen   +2 more
doaj   +1 more source

Successful management of diastolic heart failure in a patient with restrictive cardiomyopathy following an anterior communicating artery aneurysm clipping

Journal of Neuroanaesthesiology and Critical Care, 2017
Perioperative management of neurosurgical patients with an underlying myocardial dysfunction poses a unique challenge to the neuroanaesthesiologist and the neurointensivist.
Rajasekar Arumugam, Georgene Singh, Krishnaprabhu Raju, Ramamani Mariappan   +3 more
doaj   +3 more sources

Restrictive cardiomyopathy: difficulties desminopathy diagnostics

Российский кардиологический журнал, 2019
The article provides a brief overview of the problems of diagnostics and etiological verification of restrictive cardiomyopathy (RCMP). Multiple causes lead to the restrictive phenotype of intracardiac hemodynamics and diastolic dysfunction of the heart:
T. G. Vaikhanskaya, T. M. Kaptsiukh, T. V. Kurushko, L. N. Sivitskaya, O. D. Liaudanski, N. G. Danilenko   +5 more
doaj   +1 more source

Restrictive cardiomyopathy

Medicine of Ukraine, 2017
В статье рассматриваются вопросы классификации, этиологии, патогенеза, клиники, диагностики и лечения рестриктивной кардиомиопатии (РКМП) как широкого спектра заболеваний, объединенных одним патофизиологическим механизмом рестриктивной диастолической дисфункции вследствие распространенного фиброза или инфильтрации стенок желудочков различными ...
E. A. Butko, K. Yu. Kinoshenko
openaire   +4 more sources

Idiopathic restrictive cardiomyopathy - perspectives from genetics studies. Is it time to redefine these disorders?

Cardiogenetics, 2012
Idiopathic restrictive cardiomyopathy (IRC) is a rare form of heart muscle disease. Genetic studies have revealed that in about half the cases, IRC forms part of the hereditary sarcomeric contractile protein disease spectrum.
Ajay Bahl, Uma Nahar Saikia, Madhu Khullar   +2 more
doaj   +1 more source

Development of a Personalized Visualization and Analysis Tool to Improve Clinical Care in Complex Multisystem Diseases With Application to Scleroderma

Arthritis Care &Research, EarlyView.
Objective In complex diseases, it is challenging to assess a patient's disease state, trajectory, treatment exposures, and risk of multiple outcomes simultaneously, efficiently, and at the point of care. Methods We developed an interactive patient‐level data visualization and analysis tool (VAT) that automates illustration of the trajectory of a ...
Ji Soo Kim, John Scott, Lauren Fisher, Lauren N. Smith, Willie Stewart, Adrianne Woods, Rob Smithwright, Diane Koher, Parastoo Aslanbeik, Aalok B. Shah, Brad Tibbils, Samantha I. Pitts, Ayse P. Gurses, Yushi Yang, Ana‐Maria Orbai, Antony Rosen, Laura K. Hummers, Scott L. Zeger, Ami A. Shah   +18 more
wiley   +1 more source