Results 31 to 40 of about 12,761 (249)
A Case of Dextrotransposition of the Great Arteries Type I with Reversed Differential Cyanosis
Transposition of the great arteries type I is a severe congenital heart disease that induces serious cyanosis immediately after birth and death within 24 hours, unless proper treatment is administered.
Yuichi Morimoto +2 more
doaj +1 more source
A deleterious variant of FCHSD1 results in mTOR pathway overactivation and may cause porto‐sinusoidal vascular disorder (PSVD). The pedigree of the family demonstrated an autosomal dominant disease with variable expressivity. Whole‐genome sequencing and Sanger sequencing both validated the existence of the FCHSD1 variant and the heterozygosity of c ...
Jingxuan Shan +19 more
wiley +1 more source
INTRODUCTION Transposition of the great arteries is the second most common cyanotic congenital heart defect after tetralogy of Fallot. The arterial switch procedure (А. Jatene, 1975) is the surgical treatment of choice.
V. S. Selyaev +6 more
doaj +1 more source
Pulmonary Hypertension in Adults With a Systemic Right Ventricle (Biventricular Circulation)
Background: Little is known regarding pulmonary hypertension (PH) in adults with a systemic right ventricle. Objectives: This study evaluates the hemodynamic profile of PH in patients with transposition of great arteries palliated with an atrial switch ...
William M. Wilson, MBBS +41 more
doaj +1 more source
Congenitally corrected transposition of great arteries is a rare congenital anomaly. This case report describes a 30-year-old patient of congenitally corrected transposition of the great arteries with rheumatic involvement of systemic (tricuspid) atrio ...
Bharat B Kukreti +2 more
doaj +1 more source
Background In the past 3 decades, the arterial switch procedure has replaced the atrial switch procedure as treatment of choice for transposition of the great arteries.
Oktay Tutarel +10 more
doaj +1 more source
Supratricuspid obstructive membrane in congenitally corrected transposition of the great arteries
Obstructive lesions in the inflow of the systemic ventricle in congenitally corrected transposition of the great arteries are rare. It is important to identify such lesion which could alter the surgical outcome if not recognized.
Sanjeev Kumar +2 more
doaj +1 more source
Movement Disorders in Aicardi–Goutières Syndrome and Response to Immunomodulation
ABSTRACT This study characterizes movement disorders and treatment responses in seven children with Aicardi–Goutières syndrome (AGS). We retrospectively evaluated motor phenotypes, neuroimaging, and interferon signatures in patients treated with baricitinib or anifrolumab. Spasticity affected all patients, while dystonia was present in 4/7.
Enrique Gonzalez Saez‐Diez +10 more
wiley +1 more source
Situs inversus with levocardia and congenitally corrected transposition of the great arteries represents a relatively very rare congenital condition and most patients are diagnosed in infancy or early age.
Atefeh Ghorbnazadeh +5 more
doaj +1 more source
Transplantation after Mustard operation for transposition of the great arteries
As long‐term outcomes of congenital heart diseases improve, the probability of adult patients presenting for heart transplantation for late failure of congenitally corrected heart disease also increases. In patients with dextro‐transposition of the great
Shintaro Katahira +8 more
doaj +1 more source

