Progeria
What's New
Last Posted: Jan 19, 2023
- Baseline Range of Motion, Strength, Motor Function, and Participation in Youth with Hutchinson-Gilford Progeria Syndrome.
Malloy Julie et al. Physical & occupational therapy in pediatrics 2023 1-20 - The Nuclear Envelope in Ageing and Progeria.
Fragoso-Luna Adrián et al. Sub-cellular biochemistry 2023 10253-75 - Targeting the progeria mutation- Base editors correct a mutation that causes progeria in a mouse model the disease.
H Stower, Nature Medicine, January 25, 2021 - NIH Director Backs Moratorium for Heritable Genome Editing
Gen News, November 8, 2019 - The genetics of human ageing
D Melzer et al, November 5, 2019 - One Little Girl's Story Highlights the Promise of Precision Medicine
F Collins, NIH director's blog, October 23, 2019 - Hereditary Syndromes with Signs of Premature Aging.
Lessel Davor et al. Deutsches Arzteblatt international 2019 Jul 116(29-30) 489-496 - Precision Medicine and Progress in the Treatment of Hutchinson-Gilford Progeria Syndrome.
Hisama Fuki Marie et al. JAMA 2018 Apr 319(16) 1663-1664 - Can Hutchinson-Gilford progeria syndrome be cured in the future?
Rehman Neeha Abdul et al. Intractable Rare Dis Res 2015 May (2) 111-2 - Genetics of aging, progeria and lamin disorders.
Ghosh Shrestha et al. Curr. Opin. Genet. Dev. 2014 Jun 41-6
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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:Mar 27, 2024
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