Why is "DiGeorge syndrome" trending?

Search Interest Perspective

• Basal ganglia calcifications and hypocalcemic seizure in an adolescent with late-diagnosed DiGeorge syndrome - ScienceDirect.com
• The systemic effects of 22q11.2 deletion syndrome on immunity - rupress.org
• Repurposing a cholesterol drug may benefit DiGeorge syndrome patients with neuropsychiatric disease - Medical Xpress
• Right-Sided Aortic Arch Presenting as Chronic Cough in a 50-Year-Old Patient With DiGeorge Syndrome: A Report of a Rare Case - Cureus
• Harmony Freezes Cannabidiol Gel After Phase III Miss in Fragile X Syndrome - BioSpace
• This startup’s mission to extend human life sounds like sci-fi, and investors are betting $20M on it - technical.ly
• Severe Aortic Insufficiency and Cardiogenic Shock in a 16-Year-Old With DiGeorge Syndrome and Truncus Arteriosus - JACC Journals
• Born Without Immune System But With Hope - ABC News
• DiGeorge syndrome - Autism Speaks
• New study shows that a leaky blood-brain barrier causes autism-like symptoms. - Psychology Today
• Genetic Drivers of Kidney Defects in the DiGeorge Syndrome - NEJM
• A challenge of rare disease: Roanoke woman went undiagnosed for nearly seven decades - Virginia Tech News
• Abnormal developmental trajectory and vulnerability to cardiac arrhythmias in tetralogy of Fallot with DiGeorge syndrome - Nature
• Unique Considerations in the Treatment of Psychosis in DiGeorge Syndrome: A Case Report - Cambridge University Press & Assessment
• Drug-induced parkinsonism in a patient with DiGeorge syndrome: a case report - Frontiers
• Infectious Complications of DiGeorge Syndrome in the Setting of Malignancy - Cureus
• Virginia Tech scientist identifies narrow opportunity to address a disease connected with autism, schizophrenia - Virginia Tech News
• Deconstructing DiGeorge syndrome - Nature
• Hypocalcemia and a Positive Metabolic Screen for Severe Combined Immunodeficiency in an 11-Day-Old Male With DiGeorge Syndrome - Cureus
• The Outcomes of Cardiac Surgery in Children With DiGeorge Syndrome in a Single Center Experience: A Retrospective Cohort Study - Cureus
• Congenital Aplasia of the Thymus Gland (DiGeorge's Syndrome) - NEJM
• DiGeorge Syndrome Market Expected to Exhibit a CAGR Of 4.86% During 2025-2035, impelled by Advancements in Early Detection and Genetic Testing - BioSpace
• DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1 - Nature
• Unraveling Hematological Anomalies in DiGeorge Syndrome: A Retrospective Study of Thrombocytopenia and Mean Platelet Volume - Cureus
• A First Case Report of DiGeorge Syndrome from Ethiopia Highlights Challenges in Identifying and Treating Children with Primary T-Cell Deficiencies in Low Resource Settings - Wiley Online Library
• After beating the odds, Joey dreams of Hollywood - Boston Children's Answers
• Getting to the heart of DiGeorge syndrome - Nature
• Study may show a way to predict whether children with a genetic disorder will develop autism or psychosis - UCLA Health
• Is the genetic basis of DiGeorge syndrome in HAND? - Nature
• DiGeorge syndrome: Care change 'puts life at risk' says mother - BBC
• 22q11.2 deletion syndrome in diverse populations - Kruszka - 2017 - American Journal of Medical Genetics Part A - Wiley Online Library
• Facial recognition software help diagnose rare genetic disease - Medical Xpress
• Genetic and functional studies reveal genetic drivers of renal disease in DiGeorge syndrome - Nature
• Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes - The Lancet
• After Decades of Research, Drug Developed at Duke Receives FDA Approval - Duke Health
• Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome - Nature
• Transplantation of Thymus Tissue in Complete DiGeorge Syndrome - NEJM
• 22q11 Deletion Syndrome and Urogenital Manifestations: A Clinicopathological Case Report - Frontiers
• Endocrine aspects of the 22q11.2 deletion syndrome - Nature
• Functional outcomes of adults with 22q11.2 deletion syndrome - Nature
• TACG - Dove Medical Press
• Loss of Goosecoid-like and DiGeorge syndrome critical region 14 in interpeduncular nucleus results in altered regulation of rapid eye movement sleep - PNAS
• How selfies could help diagnose the rare genetic disease DiGeorge syndrome - Genetic Literacy Project
• DiGeorge syndrome can cause lifelong health issues if not diagnosed early - wndu.com
• Thymic and bone marrow output in individuals with 22q11.2 deletion syndrome - Nature
• Congenital heart disease in mice deficient for the DiGeorge syndrome region - Nature
• Grant provides hope for DiGeorge Children - Stanford Medicine
• Low risk of COVID-19 infection found among people with congenital heart disease - www.heart.org
• VEGF : A modifier of the del22q11 (DiGeorge) syndrome? - Nature
• DiGeorge syndrome, a rare genetic disease, could be diagnosed with selfies - CBS News
• Facial analysis technology helps diagnose rare genetic disease - Children's National Hospital
• Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice - Nature
• Reunion spurs follow-up study on treatment for DiGeorge syndrome - Findings show efficacy of bone marrow transplantation - UCLA Health
• Facial recognition software helps diagnose rare genetic disease - National Human Genome Research Institute (NHGRI) (.gov)
• Autoimmune hemolytic anemia associated with vitamin B12 deficiency and viral illness in DiGeorge syndrome. Case report and literature review - Wiley Online Library
• DiGeorge Syndrome (IMAGE) - EurekAlert!
• A CRISPR-engineered isogenic model of the 22q11.2 A-B syndromic deletion - Nature
• Transcriptional Regulation of Cardiac Development: Implications for Congenital Heart Disease and DiGeorge Syndrome - Nature
• DGCR6 at the proximal part of the DiGeorge critical region is involved in conotruncal heart defects - Nature
• Families with Children living with DiGeorge Syndrome Unite - Spectrum News
• CRKL in 22q11.2; a key gene that contributes to common birth defects - Baylor College of Medicine Blog Network -
• Autism Spectrum Disorders, Down Syndrome, and 22q Deletion Syndrome - Psychiatric Times
• iGeorge syndrome kidney problems may be caused by missing gene - Medical Xpress
• Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome - psychiatryonline.org
• Radiology In Ped Emerg Med, Vol 2, Case 2 - University of Hawaii System
• 22q11.2 deletion syndrome raises risk of early Parkinson’s by 6 times - Parkinson's News Today
• Prenatal diagnosis of the 22q11.2 deletion syndrome - Nature
• Sick baby is Michigan's first to undergo thymus transplant - Detroit Free Press
• After Decades of Research, Drug Developed at Duke Receives FDA Approval - Duke University School of Medicine
• Swallowing Difficulties May Be Caused by Misfiring Neurons - Genetic Engineering and Biotechnology News
• ‘We were told, ‘She may not be born breathing.’ Scared was an understatement.’: Mom gives birth to baby with DiGeorge syndrome, ‘She’s our miracle’ - Love What Matters
• 'I thought I would have to say goodbye': Ashleigh celebrates first Mother's Day with Xavier - Australian Broadcasting Corporation
• When They Warn of Rare Disorders, These Prenatal Tests Are Usually Wrong (Published 2022) - The New York Times
• Schizophrenia and velo-cardio-facial syndrome - The Lancet
• DCHS senior with DiGeorge Syndrome receives fairytale prom proposal - The Owensboro Times
• Born with a rare genetic defect, photojournalist Nadia Zomorodian never quit fighting - Daytona Beach News-Journal
• Inherited thrombocytopenias - Haematologica
• Growth charts for 22q11 deletion syndrome - Tarquinio - 2012 - American Journal of Medical Genetics Part A - Wiley Online Library
• DiGeorge syndrome Gene disorder can be fatal for babies - The Oklahoman
• Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome - PNAS
• New research at Cardiff University finds children with rare genetic condition may need early developmental support - Cardiff University
• How to predict development of autism or psychosis - healthcare-in-europe.com
• Understanding kids and heart disease: DiGeorge syndrome - AL.com
• DiGeorge Medal honors genetics expert for longstanding work on chromosome deletion syndrome - EurekAlert!
• Aurora man’s survival mystifying - The Denver Post
• CRKL in 22q11.2; a key gene that contributes to common birth defects - Medical Xpress
• Furry friend helps lift spirits of girl with rare genetic disorder - 11Alive.com
• Rifle family in Denver while newborn battles rare heart condition - Denver7
• Mercy’s Story: Living life with 22q, a genetic condition - WECT
• Sleep problems in children with genetic condition linked to multiple health issues - Medical Xpress
• Doctor: La Vergne infant who starved had heart condition - The Daily News Journal
• Facial recognition software can diagnose rare genetic disease with 96% accuracy - ZME Science
• Doctors said the boy was suffering from teenage psychosis. What he really had was a rare genetic condition. - The Washington Post
• FDA Issues Warning About Large Percentage Of False Positives In Prenatal Screening Tests - Scary Mommy
• 22q11.2: Mystery disease that has no name and no cure - India Today
• Thymus transplants treat children with severe immunodeficiency - Agência FAPESP
• A St. Christopher's pioneer on ailment - Inquirer.com
• Brave and ‘cheeky’ Elliot’s very special day out - Herald Sun
• 'It would be such a massive relief' - Mum pushes for UK-first centre to help son - Nwemail.co.uk
• Baby girl had open heart surgery when she was just six days old - Wales Online