Progeria: A Rare Genetic Syndrome

V Sharma, R Shukla - Indian Journal of Clinical Biochemistry, 2020 - Springer
An uncommon deadly genetic situation symbolized by the presence of rapid maturation in
infants is called as the Hutchinson–Gilford Progeria Syndrome. The term basically is meant …

Neurovascular syndromes

KA Keith, LK Reed, A Nguyen… - Neurosurgery …, 2022 - neurosurgery.theclinics.com
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AI-ECG and the Prediction of Accelerated Aging

RJ Pignolo - Mayo Clinic Proceedings, 2023 - mayoclinicproceedings.org
The paper by Shelly et al 1 in this issue of Mayo Clinic Proceedings represents a next step in
our understanding of artificial intelligence (AI) einterpreted electrocardiogram (ECG) …

Accelerated aging in patients with Hutchinson-Gilford progeria syndrome: Clinical signs, molecular causes, treatments, and insights into the aging process

J Parreno, AV Cruz - UBC Medical Journal, 2011 - ojs.library.ubc.ca
Abstract Hutchinson-Gilford Progeria Syndrome (HGPS) is a condition characterized by
signs of accelerated aging that present within the first year of life. Notable characteristics of …

[HTML][HTML] Novel LMNA mutations in Greek and Myanmar patients with progeroid features and cardiac manifestations

R Kandhaya-Pillai, FM Hisama, SA Bucks… - Aging pathobiology …, 2020 - ncbi.nlm.nih.gov
Segmental progeroid syndromes are groups of genetic disorders with multiple features
resembling accelerated aging. The International Registry of Werner Syndrome (Seattle, WA) …

3. ハッチンソン・ギルフォード早老そうろう症候群しょうこうぐん

井原いはら健二けんじ - 日本にっぽん老年ろうねん学会がっかい雑誌ざっし, 2021 - jstage.jst.go.jp
抄録しょうろく ハッチンソン・ギルフォード早老そうろう症候群しょうこうぐん遺伝いでんせい早老そうろうしょうなかでもちょう希少きしょう (ぜん世界せかいで 350~ 400
ひと) かつとくじゅうあつし (平均へいきん寿命じゅみょうは 14.6 さい) な疾患しっかんである. LMNA 遺伝子いでんしのエクソン 11 …

New vascular insights into premature aging

CJ Lowenstein, JA Bennett - The Journal of Clinical …, 2019 - Am Soc Clin Investig
Hutchinson-Gilford progeria syndrome (HGPS) is a fatal disease characterized by premature
aging in which young children fail to thrive and adolescents die from myocardial infarction or …

Regulation of antioxidant Nrf2 signaling: an important pathway in COPD

N Chatterjee, D Chatterjee - Oxidative Stress in Lung Diseases: Volume 2, 2020 - Springer
Oxidative stress plays a role in multiple disorders that include lung diseases like chronic
obstructive pulmonary disease (COPD) and asthma. The Nrf2 signaling pathway is the …

A Growth-Restricted Neonate with Abnormal Facies and Lax Skin

S Jyothi, RR Prashanth, S Nair… - NeoReviews, 2024 - publications.aap.org
DISCUSSION The Condition HGPS is a rare fatal sporadic autosomal dominant
laminopathy, with no ethnic predisposition. The prevalence has been estimated as 1 in 20 …

[PDF][PDF] A Pair of Sibling Patients With Premature Aging Syndrome of Unknown Etiology

K Iwai, M Okawada - Cureus, 2024 - cureus.com
Premature aging syndrome is a rare condition characterized by premature aging and death.
The exact pathogenic mechanisms underlying most premature aging syndromes are poorly …