Shi-Joon Yoo^1,2,*, Ankavipar Saprungruang², Christopher Z. Lam¹, Robert H. Anderson³

Congenital Heart Disease, Vol.17, No.5, pp. 495-504, 2022, DOI:10.32604/chd.2022.021155 - 06 September 2022

Abstract In the last issue, two case reports separately present examples of the extremely rare and complex congenital heart diseases that show concordant atrioventricular connections to the L-looped ventricles in the presence of situs solitus. Both cases highlight that the relationship between the two ventricles within the ventricular mass is not always harmonious with the given atrioventricular connection. Such disharmony between the connections and relationships requires careful assessment of the three basic facets of cardiac building blocks, namely their morphology, the relationship of their component parts, and their connections with the adjacent segments. 3D imaging and printing can More > Graphic Abstract

Maqsood Ahmad^1,2, Noorhaniza Wahid¹, Rahayu A Hamid¹, Saima Sadiq², Arif Mehmood³, Gyu Sang Choi^4,*

CMC-Computers, Materials & Continua, Vol.72, No.3, pp. 5041-5058, 2022, DOI:10.32604/cmc.2022.026077 - 21 April 2022

Abstract Mental health signifies the emotional, social, and psychological well-being of a person. It also affects the way of thinking, feeling, and situation handling of a person. Stable mental health helps in working with full potential in all stages of life from childhood to adulthood therefore it is of significant importance to find out the onset of the mental disease in order to maintain balance in life. Mental health problems are rising globally and constituting a burden on healthcare systems. Early diagnosis can help the professionals in the treatment that may lead to complications if they… More >

Tarek A ATIA

BIOCELL, Vol.43, No.4, pp. 253-262, 2019, DOI:10.32604/biocell.2019.08180

Abstract Recurring miscarriage (RM) is a frustrating reproductive complication with variable etiology. Numerous genetic defects have been known to play a crucial role in the etiology of RM. Chromosomal abnormalities are frequently detected, while other genetic defects cannot be diagnosed through routine research, such as cryptic chromosomal anomalies, single nucleotide polymorphism, single-gene defect, and gene copy number variation. Diagnostic laboratories have recently used variable advanced techniques to detect potential genetic abnormalities in couples with RM and/or in products of conception. Here we aim to summarize the known genetic causes of RM, with a focus on the More >