Zobrazeno 1 - 10
of 4 269
pro vyhledávání: '"Ventriculomegaly"'
Autor:
Amenu Diriba, Temesgen Tilahun, Lammii Gonfaa, Jemal Gebi, Bikila Lemi, Jiregna Fyera, Suleiman Mazeng, Aschalew Legesse, Dinaol Alemu
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-4 (2024)
Abstract Background When a pregnant mother finds out she has a fetus with a congenital defect, the parents feel profound worry, anxiety, and melancholy. Anomalies can happen in singleton or twin pregnancies, though they are more common in twin pregna
Externí odkaz:
https://doaj.org/article/5937b30069a343a4a678b699b484ae75
Publikováno v:
Physiologia, Vol 4, Iss 2, Pp 182-201 (2024)
Hydrocephalus is caused by an overproduction of cerebrospinal fluid (CSF), an obstruction of fluid movement, or improper reabsorption. CSF accumulation in the brain’s ventricles causes ventriculomegaly, increased intracranial pressure, inflammation
Externí odkaz:
https://doaj.org/article/7b954bfcc01e4a51b6bec4aea97da5b2
Publikováno v:
European Journal of Medical Research, Vol 29, Iss 1, Pp 1-9 (2024)
Abstract Background Mild fetal ventriculomegaly (VM) is a nonspecific finding common to several pathologies with varying prognosis and is, therefore, a challenge in fetal consultation. We aimed to perform a constant, detailed analysis of prenatal fin
Externí odkaz:
https://doaj.org/article/e06a7f8652974e3e9e61ac011f36ab17
Autor:
Sweta Swaika
Publikováno v:
Indian Journal of Neonatal Medicine and Research, Vol 12, Iss 01, Pp 08-11 (2024)
Introduction: Spinal dysraphism includes a diverse collection of congenital spinal abnormalities that occur due to flawed closure of the neural tube and can be classified as open or closed types. The most common form of open spinal dysraphism is Myel
Externí odkaz:
https://doaj.org/article/7126031d17694febbe16820986385ccf
Publikováno v:
Children, Vol 11, Iss 8, p 957 (2024)
Fetal ventriculomegaly (VM) is a defect of the central nervous system, typically diagnosed during the second-trimester ultrasound in fetuses with an atrial diameter (AD) of >10 mm. Non-isolated ventriculomegaly (NIVM) is heterogeneous in nature, coex
Externí odkaz:
https://doaj.org/article/6b71635415ed4832b61a38de8ae91143
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
ObjectiveGenetic etiology plays a critical role in fetal ventriculomegaly (VM). However, the studies on chromosomal copy number variants (CNVs) in fetal VM are limited. This study aimed to investigate the chromosomal CNVs in fetuses with mild to mode
Externí odkaz:
https://doaj.org/article/8d7f4285353244e2979c2c38c4a6eff2
Autor:
Sara Diana Lolansen, Dagne Barbuskaite, Fenghui Ye, Jianming Xiang, Richard F. Keep, Nanna MacAulay
Publikováno v:
Fluids and Barriers of the CNS, Vol 20, Iss 1, Pp 1-11 (2023)
Abstract Background Hydrocephalus constitutes a complex neurological condition of heterogeneous origin characterized by excessive cerebrospinal fluid (CSF) accumulation within the brain ventricles. The condition may dangerously elevate the intracrani
Externí odkaz:
https://doaj.org/article/bca1c04384ae46d8951daa5d63c3bcaa
Autor:
Virág Bartek, István Szabó, Ágnes Harmath, Gábor Rudas, Tidhar Steiner, Attila Fintha, Nándor Ács, Artúr Beke
Publikováno v:
Children, Vol 11, Iss 7, p 797 (2024)
Introduction: The corpus callosum is one of the five main cerebral commissures. It is key to combining sensory and motor functions. Its structure can be pathological (dysgenesis) or completely absent (agenesis). The corpus callosum dys- or agenesis i
Externí odkaz:
https://doaj.org/article/2d0c3112a1d94376984bf845032f16a5
Autor:
Volodymyr V. Popov, Oleksandr O. Bolshak, Valery Zh. Boukarim, Olena V. Khoroshkovata, Oleksii M. Gurtovenko, Evgen V. Novikov
Publikováno v:
Український журнал серцево-судинної хірургії, Vol 31, Iss 2, Pp 16-24 (2023)
The aim. To analyze the results of introduction of complex reconstruction of the left and right parts of the heart in Marfan syndrome combined with mitral-tricuspid insufficiency, biatriomegaly and left ventriculomegaly. Materials and methods. As
Externí odkaz:
https://doaj.org/article/3411e157568e492889b696e21d23b301
Autor:
Farrah N. Brown, Eri Iwasawa, Crystal Shula, Elizabeth M. Fugate, Diana M. Lindquist, Francesco T. Mangano, June Goto
Publikováno v:
Fluids and Barriers of the CNS, Vol 20, Iss 1, Pp 1-19 (2023)
Abstract Background Neonatal hydrocephalus is a congenital abnormality resulting in an inflammatory response and microglial cell activation both clinically and in animal models. Previously, we reported a mutation in a motile cilia gene, Ccdc39 that d
Externí odkaz:
https://doaj.org/article/47e6231a38094abf9e1435ce3797e875