DiGeorge Syndrome Latest Advances

Three-dimensional craniofacial and airway morphology in paediatric patients with 22q11.2 deletion syndrome: a CBCT study with correlation to velopharyngeal dysfunction.

Journal: European journal of paediatric dentistry

Published: June 05, 2026

The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site Study.

Journal: medRxiv : the preprint server for health sciences

Published: June 04, 2026

The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site Study.

Journal: medRxiv : the preprint server for health sciences

Published: June 04, 2026

Left pulmonary artery from the common carotid artery in DiGeorge syndrome: a case of ductal stenting as bridge to repair.

Journal: Cardiology in the young

Published: June 02, 2026

Human neuromodulatory assembloids to study serotonin signaling and disease.

Journal: bioRxiv : the preprint server for biology

Published: April 10, 2026

Clinical and genetic spectrum of SHOX deficiency: phenotypic heterogeneity and the "Jumping SHOX" phenomenon.

Journal: European journal of pediatrics

Published: April 10, 2026

Prenatal Ultrasound Diagnosis of a Rare Vascular Ring Formed by Left Aortic Arch and Right Ductus Arteriosus: A Case Report.

Journal: Fetal and pediatric pathology

Published: March 31, 2026

Developmental Regression of Motor Ability in the Patient With Interruption of the Aortic Arch: Juvenile Idiopathic Arthritis Associated With Deletion of 22q11.2 Syndrome.

Journal: Cureus

Published: March 30, 2026

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Journal: medRxiv : the preprint server for health sciences

Published: March 27, 2026

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Journal: medRxiv : the preprint server for health sciences

Published: March 27, 2026

Mandibular trabecular microarchitecture as a radiographic biomarker of bone health in children with 22q11.2 deletion syndrome.

Journal: BMC pediatrics

Published: March 18, 2026

Ruptured Sinus of Valsalva Aneurysm in a Patient with DiGeorge Syndrome: Expanding the Cardiovascular Phenotype.

Journal: The Israel Medical Association journal : IMAJ

Published: March 09, 2026

DiGeorge Syndrome Latest Advances

Find the Latest Research About DiGeorge Syndrome

Three-dimensional craniofacial and airway morphology in paediatric patients with 22q11.2 deletion syndrome: a CBCT study with correlation to velopharyngeal dysfunction.

Three-dimensional craniofacial and airway morphology in paediatric patients with 22q11.2 deletion syndrome: a CBCT study with correlation to velopharyngeal dysfunction.

The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site Study.

The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site Study.

The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site Study.

The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site Study.

Left pulmonary artery from the common carotid artery in DiGeorge syndrome: a case of ductal stenting as bridge to repair.

Left pulmonary artery from the common carotid artery in DiGeorge syndrome: a case of ductal stenting as bridge to repair.

Human neuromodulatory assembloids to study serotonin signaling and disease.

Human neuromodulatory assembloids to study serotonin signaling and disease.

Clinical and genetic spectrum of SHOX deficiency: phenotypic heterogeneity and the "Jumping SHOX" phenomenon.

Clinical and genetic spectrum of SHOX deficiency: phenotypic heterogeneity and the "Jumping SHOX" phenomenon.

Prenatal Ultrasound Diagnosis of a Rare Vascular Ring Formed by Left Aortic Arch and Right Ductus Arteriosus: A Case Report.

Prenatal Ultrasound Diagnosis of a Rare Vascular Ring Formed by Left Aortic Arch and Right Ductus Arteriosus: A Case Report.

Developmental Regression of Motor Ability in the Patient With Interruption of the Aortic Arch: Juvenile Idiopathic Arthritis Associated With Deletion of 22q11.2 Syndrome.

Developmental Regression of Motor Ability in the Patient With Interruption of the Aortic Arch: Juvenile Idiopathic Arthritis Associated With Deletion of 22q11.2 Syndrome.

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Mandibular trabecular microarchitecture as a radiographic biomarker of bone health in children with 22q11.2 deletion syndrome.

Mandibular trabecular microarchitecture as a radiographic biomarker of bone health in children with 22q11.2 deletion syndrome.

Ruptured Sinus of Valsalva Aneurysm in a Patient with DiGeorge Syndrome: Expanding the Cardiovascular Phenotype.

Ruptured Sinus of Valsalva Aneurysm in a Patient with DiGeorge Syndrome: Expanding the Cardiovascular Phenotype.