Zobrazeno 1 - 10
of 2 285
pro vyhledávání: '"Left ventricular noncompaction"'
Autor:
Arumugom Archana, Chandra Kumar Natarajan, Vaanathi Hementha Kumar, Gnanasambandam Subramaniyam, Bala Ramachandran, Komarakshi Balakrishnan, KG Suresh Rao, Abhishek Berwal, Vishwanath Nandyala, Swati Iyer
Publikováno v:
Annals of Pediatric Cardiology, Vol 17, Iss 1, Pp 81-84 (2024)
A neonate born of third-degree consanguineous marriage presented on day 12 of life with congestive cardiac failure. A male sibling died at 3 months of age, cause of which was not known. He was treated with decongestive measures and multiple inotropes
Externí odkaz:
https://doaj.org/article/ea8a63f7b9734e58bfd5b70c972ff6fd
Publikováno v:
Кардиоваскулярная терапия и профилактика, Vol 23, Iss 2 (2024)
Introduction. Left ventricular noncompaction (LVNC) is a rare heterogeneous pathology characterized by a two-layered structure with a predominance of non-compact layer in the form of multiple trabeculations and pockets between them, communicating wit
Externí odkaz:
https://doaj.org/article/edb84e8da0364c56906a1ba485b83f74
Autor:
Anna Bukaeva, Roman Myasnikov, Olga Kulikova, Alexey Meshkov, Anna Kiseleva, Anna Petukhova, Evgenia Zotova, Peter Sparber, Alexandra Ershova, Evgeniia Sotnikova, Maria Kudryavtseva, Anastasia Zharikova, Sergey Koretskiy, Elena Mershina, Vasily Ramensky, Marija Zaicenoka, Yuri Vyatkin, Alisa Muraveva, Alexandra Abisheva, Tatiana Nikityuk, Valentin Sinitsyn, Mikhail Divashuk, Elena Dadali, Maria Pokrovskaya, Oxana Drapkina
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 14, p 7556 (2024)
A genetic diagnosis of primary cardiomyopathies can be a long-unmet need in patients with complex phenotypes. We investigated a three-generation family with cardiomyopathy and various extracardiac abnormalities that had long sought a precise diagnosi
Externí odkaz:
https://doaj.org/article/e5f8369f251a415b864ae0aeb61178b7
Publikováno v:
BMC Cardiovascular Disorders, Vol 23, Iss 1, Pp 1-5 (2023)
Abstract Background Left ventricular noncompaction (LVNC) is a specific type of cardiomyopathy characterized by coarse trabeculae and interspersed trabecular crypts within the ventricles. Clinical presentation varies widely and may be nonsignificant
Externí odkaz:
https://doaj.org/article/8379de3cbf4e46c7879c2e0badf3f252
Publikováno v:
Journal of the Indian Academy of Echocardiography & Cardiovascular Imaging, Vol 7, Iss 3, Pp 250-254 (2023)
A 61-year-old male with no significant medical history presented with dyspnea on exertion for the past 3 months. Clinical examination findings and electrocardiogram showed sinus rhythm and left ventricular hypertrophy. The chest X-ray and basic labor
Externí odkaz:
https://doaj.org/article/a8d7d23814f54165a68a1d6c1c680da8
Publikováno v:
Pediatric Discovery, Vol 1, Iss 2, Pp n/a-n/a (2023)
Abstract Left ventricular noncompaction (LVNC) is a heterogeneous disorder with unclear genetic causes. The arhGEF18 gene is a guanine nucleotide exchange factor related to the Rho pathway and a possible predisposing gene for LVNC. In this study, a m
Externí odkaz:
https://doaj.org/article/6ec3d60e192a40cea35f09f32fe6c393
Autor:
Jingdong Li, Wanyue Zhu, Guanhua Su, Feng Zhu, Xinxin Shuai, Yidi Meng, Jiaming Zhang, Hao Chen
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundBecker muscular dystrophy (BMD) is an inherited X-linked recessive condition resulting from mutations of the DMD gene encoding dystrophin. Left ventricular noncompaction (LVNC) is a rare cardiomyopathy morphologically characterized by abnor
Externí odkaz:
https://doaj.org/article/9d99e567ac2a464291e0e3aa2c64ef74
Autor:
Wei Bai, Rong Xu, Xiao Li, Huayan Xu, Hang Fu, Ruilai Hou, Ziqi Zhou, Wei Huang, Yining Wang, Yingkun Guo
Publikováno v:
BMC Cardiovascular Disorders, Vol 22, Iss 1, Pp 1-11 (2022)
Abstract Background Cardiac magnetic resonance (CMR) has been used to diagnose and risk-stratify patients with left ventricular noncompaction (LVNC). The prognostic value of CMR parameters for LVNC, especially feature tracking (CMR-FT), is not well k
Externí odkaz:
https://doaj.org/article/f58ce3f201e44d958a4e23da679523f3
Autor:
Atsuhito Takeda, Masahiro Ueki, Jiro Abe, Kazuhiro Maeta, Tomoko Horiguchi, Hirokuni Yamazawa, Gaku Izumi, Ayako Chida‐Nagai, Daisuke Sasaki, Takao Tsujioka, Itsumi Sato, Masahiro Shiraishi, Masafumi Matsuo
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 7, Pp n/a-n/a (2023)
Abstract Barth syndrome (BTHS) is an X‐linked disorder characterized by cardiomyopathy, skeletal myopathy, and 3‐methylglutaconic aciduria. The causative pathogenic variants for BTHS are in TAZ, which encodes a putative acyltransferase named tafa
Externí odkaz:
https://doaj.org/article/fdbcd61460324c7a9ce70a09275b62e3
Autor:
Hiroshi Kawamura, Masamichi Ikawa, Keiichi Hirono, Junya Kimura, Takashi Okuno, Masao Kawatani, Kunihiro Inai, Yukiko Hata, Naoki Nishida, Yoshio Yoshida
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundLeft ventricular noncompaction (LVNC) is a rare inherited cardiomyopathy with a broad phenotypic spectrum. The genotype-phenotype correlations in fetal-onset LVNC have not yet been fully elucidated. In this report, we present the first case
Externí odkaz:
https://doaj.org/article/906b3b58f7744e1198c679e0ae25c4f4