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http://dx.doi.org/10.1097/ALN.0000000000002258 | DOI Listing |
J Cardiothorac Surg
January 2025
Department of Cardiovascular Surgery, Sapporo Cardio Vascular Clinic, 8-1, Kita 49 jyo, Higashi 16 jyo, Higashi-ku, Sapporo, Hokkaido, 007-0849, Japan.
Background: Minimally invasive cardiac surgery for mitral regurgitation is challenging in patients with narrow chests due to limited thoracic space. The butterfly technique can prevent systolic anterior motion in patients with degenerative mitral regurgitation and redundant posterior leaflets, but it is difficult to perform via minimally invasive cardiac surgery. Few reports have described mitral valve repair using the butterfly technique or in a narrow chest.
View Article and Find Full Text PDFBMC Med Genomics
December 2024
Prenatal Diagnosis Center, Quanzhou Women's and Children's Hospital, Quanzhou, Fujian Province, 362000, China.
Background: The literature contains exceedingly limited reports on chromosome 10p15.3 microdeletions. In the present study, two cases of fetuses with pure terminal 10p15.
View Article and Find Full Text PDFZootaxa
April 2024
El Colegio de la Frontera Sur; Unidad Chetumal Av. Centenario Km 5.5; CP 77014 Chetumal; Quintana Roo; Mexico.
Despite the threat that lionfishes pose to non-native marine ecosystems worldwide, their early life stages (ELS) remain difficult to distinguish from morphologically similar taxa due to inadequate descriptions and poorly defined taxonomic characters. Two members of the Indo-Pacific marine assemblage commonly known as lionfishes, zebrafishes, firefishes, turkeyfishes, and butterfly-cods (Scorpaeniformes: Scorpaenidae: Pteroinae) are invasive in the Western North Atlantic (WNA). Here, we describe the ELS of Pterois volitans, Dendrochirus barberi, and two transforming larvae and an early juvenile of D.
View Article and Find Full Text PDFExp Clin Transplant
October 2024
From the Division of Transplantation, Department of General Surgery, Baskent University, Ankara, Turkey.
Objectives: Alagille syndrome is an autosomal recessive disorder with multisystemic involvement. Patients with Alagille syndrome have many accompanying anomalies such as atypical facial appearance, posterior embryotoxon, butterfly vertebra, cardiac anomalies, and biliary problems. Liver and heart complications can determine the mortality and morbidity of patients with Alagille syndrome.
View Article and Find Full Text PDFRev Prat
October 2024
Service de rhumatologie, CHU Ibn Rochd, faculté de médecine et de pharmacie, université Hassan II, Casablanca, Maroc.
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