Wagr Syndrome
What's New
Last Posted: May 15, 2023
- Visual Acuity in Aniridia and WAGR Syndrome.
Michael A Krause, et al. Clinical ophthalmology (Auckland, N.Z.) 2023 0 1255-1261 - A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977?kb deletion in the 11p13 region.
Vasilyeva Tatyana A, et al. BMC medical genomics 2020 0 (Suppl 8) 130 - Results From the WAGR Syndrome Patient Registry: Characterization of WAGR Spectrum and Recommendations for Care Management.
Duffy Kelly A et al. Frontiers in pediatrics 2021 9733018 - CLINGEN Actionability Report for Wilms tumor-WT1
ClinGen Actionability Working Group - Rare Syndromes and Common Variants of the Brain-Derived Neurotrophic Factor Gene in Human Obesity.
Han J C, et al. Progress in molecular biology and translational science 2016 0 75-95 - WAGR syndrome
From NCATS Genetic and Rare Diseases Information Center - Brain-derived neurotrophic factor and obesity in the WAGR syndrome.
Han Joan C, et al. The New England journal of medicine 2008 8 (9) 918-27 - WT1 gene analysis in sporadic early-onset and bilateral wilms tumor patients without associated abnormalities.
Perotti Daniela, et al. Journal of pediatric hematology/oncology 2005 4 (4) 197-201
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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
- Page last updated:May 30, 2024
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