Sudden Sensorineural Hearing Loss
What's New
Last Posted: Jan 12, 2025
- Causal relationship between psoriasis and sudden deafness: a Mendelian randomization study.
Linrong Wu, et al. Archives of dermatological research 2025 0 (1) 167 - Evaluation of angiotensin converting enzyme insertion/deletion, alpha adducin (ADD1) G460W, and IL-10 gene polymorphisms, and determination of prognostic effects in idiopathic sudden sensorineural hearing loss.
Vural Ak?n, et al. Journal of otology 2024 0 (2) 97-105 - Causal associations of white blood cell count and sudden sensorineural hearing loss: a bidirectional and multivariable Mendelian randomization study.
Ling Zhang, et al. Frontiers in neurology 2024 0 1387244 - Bidirectional causality between idiopathic sudden sensorineural hearing loss and depression: a Mendelian randomization study.
Chuanyu Wu, et al. Scientific reports 2024 0 (1) 14932 - Paradoxical Embolism in Juveniles and Young Adults With Severe-to-Profound Sudden Sensorineural Hearing Loss.
Huiying Sun, et al. Ear, nose, & throat journal 2024 0 1455613241250185 - Assessing risk of stroke after idiopathic sudden sensorineural hearing loss using data from general practice.
Fieke K Oussoren, et al. Scientific reports 2024 0 (1) 10026 - Causal role of immune cell phenotypes in idiopathic sudden sensorineural hearing loss: a bi-directional Mendelian randomization study.
Wanqing Li, et al. Frontiers in neurology 2024 0 1368002 - A Systematic Review on Heritability of Sudden Sensorineural Hearing Loss.
Mª Á Yélamos Lorente, et al. The Laryngoscope 2024 0 - Causal associations of thyroid function and sudden sensorineural hearing loss: a bidirectional and multivariable Mendelian randomization study.
Jialei Chen, et al. Frontiers in neurology 2023 0 1269545 - Machine Learning Models for Predicting Sudden Sensorineural Hearing Loss Outcome: A Systematic Review.
Amirhossein Aghakhani et al. Ann Otol Rhinol Laryngol 2023 34894231206902
More
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Content source: