Cautious Hope for Endovascular Aortic Tx in Connective Tissue Disease Success observed in usually contraindicated Marfan, Loeys-Dietz syndromes Jun 14, 2023
Full-On Reversal of Cardiac Amyloidosis Possible With Antibodies Future treatments don't have to be limited to slowing disease, case series suggests Jun 07, 2023
Rare Skin Blistering Condition Gets First Drug Approved FDA's decision marks first approval for a redosable gene therapy May 19, 2023
FDA 'Leans In' to Accelerated Approval for Rare Disease Drugs CBER director says "moment is tender for gene therapy," sees opportunity to "salvage" treatments May 19, 2023
Alzheimer's Progression Delayed by Rare Genetic Variant Finding challenges previous assumptions about disease May 15, 2023
B-Cell Stimulating Factors Tied to Lymphoma in Sjogren's Findings may bolster interest in BTK inhibitors for autoimmune diseases May 02, 2023
FDA Extends Trikafta Approval to Even Younger Cystic Fibrosis Patients Patients ages 2 to 5 years now eligible for the triple therapy Apr 27, 2023
Genomics Add Insight Into Worse Colorectal Cancer Outcomes in Black Patients Fewer actionable mutations, less likely to meet genomic criteria for immunotherapy Apr 19, 2023
Many With Cancer Predisposition Diseases Unaware of Genetic Status Moreover, a significant proportion do not qualify for genetic screening under current guidelines Apr 19, 2023
Oral Drug Improves Sunlight Tolerance in Genetic Photosensitivity Disorders Dersimelagon significantly extended time to sun-related prodromal symptoms Apr 12, 2023
Genomics Can Help Diagnose Rare Pediatric Diseases Large study found genomic analysis delivered answers for 41% of kids with undiagnosed disease Apr 12, 2023
NIH's Genome Chief Says Genomics Is Evolving and Docs Need More Education on It National Human Genome Research Institute Director Eric Green sits down with 51˶ Apr 07, 2023
A 'Double Whammy' for Gastric Cancer Risk H. pylori infection and certain pathogenic variants linked with large excess risk Mar 29, 2023
Common Enzyme Deficiency Linked With COVID Severity Certain groups of men with G6PD deficiency had higher odds of severe illness Mar 29, 2023
FDA Greenlights First Drug for Rare Immunodeficiency Disease Activated PI3K-delta syndrome may have a new standard of care Mar 27, 2023
Investigational ALS Drug May Have Clinical Benefit, FDA Staff Says Neurofilament light will be evaluated as a surrogate endpoint in tofersen review Mar 20, 2023
Fetus Removed From Brain of 1-Year-Old Girl Intracranial fetus-in-fetu identified in child with motor delay Mar 09, 2023
Expanding ICD Codes May Aid Rare Disease Patients, Research NCATS explores how best to use diagnostic codes to move field forward Mar 02, 2023
First Treatment Approved for Rare Neurodegenerative Disorder Omaveloxolone gets FDA nod for Friedreich's ataxia Mar 01, 2023
FDA OKs First Therapy for Alpha-Mannosidosis Velmanase alfa approved for treating non-CNS manifestations of progressive, inherited disease Feb 17, 2023
Rare Disease Non-Profit Shows Drug Development Savvy FAST sold a drug candidate to seed other treatment strategies for Angelman syndrome Feb 15, 2023
Does the Environment Override Genes for People at Risk of Stroke? Large study detects interaction between genetic susceptibility and neighborhood deprivation Feb 08, 2023
Inflammatory VEXAS Syndrome May Not Be So Uncommon Is new disease being missed by physicians? Jan 24, 2023
Genomic Assay May Pinpoint Who Can Skip RT After Breast-Conserving Surgery Patients categorized as low risk with 16-gene signature showed no significant benefit with RT Jan 06, 2023
Dementia Accompanying Cardiometabolic Disease: Does It Come Down to Genetics? Twin study suggests special monitoring in some individuals Dec 29, 2022
Families Push Research Forward in Rare Diseases The field has a unique funding model. While fruitful, some question if it needs to change. Dec 26, 2022
COVID Vaccines Made mRNA a Household Name. How Can It Help in Rare Diseases? A handful of companies have mRNA therapies in human trials for rare diseases Dec 26, 2022
Early Win for Gene Therapy in Rare Form of SCID 10 infants were able to make their own T cells; safety good so far Dec 21, 2022
Topical Gene Therapy Heals Blistering Skin Disease Lesions Randomized trial shows "dramatic" benefits in rare genetic disease Dec 14, 2022
Assay Predicts Breast Cancer Patients Who Will Benefit From Ovarian Suppression Low score suggests improved outcomes with ovarian suppression plus adjuvant endocrine therapy Dec 07, 2022
Decoding Cancer A conversation with Harold Varmus, MD, who received the Nobel Prize in Physiology or Medicine in 1989 Dec 06, 2022 podcast
Chris Hemsworth's APOE4 Alzheimer's Gene The Thor actor recently learned about his genetic predisposition Dec 01, 2022
FDA OKs First Gene Therapy for Hemophilia B Hemgenix reduced rate of annual bleeds, eliminated need for factor IX prophylaxis therapy Nov 22, 2022
Early Cardiac Amyloidosis Still Bad News Without Treatment Observational study supports treating even asymptomatic patients Nov 16, 2022
CRISPR Shows Promise for Hereditary Angioedema in First-in-Human Trial No safety concerns reported and swelling attacks declined Nov 15, 2022
Promising Results in First Test of In Utero Enzyme-Replacement Therapy Treatment was safe, effective in one baby with infantile-onset Pompe disease Nov 09, 2022
Texas Says DNA Kits for Schoolchildren Not Tied to Uvalde Shooting State education agency says effort was designed to help law enforcement find missing kids Oct 27, 2022
Gene Therapy for Degenerative Brain Disorder Wins FDA Nod $3 million price tag for one-time treatment Sep 19, 2022
Blood Type Tied to Early-Onset Stroke Risk Findings point to prothrombotic mechanisms in younger stroke patients Sep 01, 2022
Pralsetinib Shows Promise in Diverse RET Fusion-Positive Cancers An ORR of 57% supports results previously observed in NSCLC and thyroid cancer Aug 26, 2022
