Patent Ductus Arteriosus
What's New
Last Posted: Nov 05, 2024
- The association of gene polymorphisms of adenosine and dopamine receptors with the response to caffeine citrate treatment in infants with apnea of prematurity: a prospective nested case-control study.
Jiangbiao Xie, et al. Italian journal of pediatrics 2024 0 (1) 225 - Missense mutations in the CITED2 gene may contribute to congenital heart disease.
Hira Yaqoob, et al. BMC cardiovascular disorders 2024 0 (1) 516 - High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects.
Gloria K E Zodanu et al. Int J Mol Sci 2024 25(10) - Illuminating the Genetic Basis of Congenital Heart Disease in Patients with Kabuki Syndrome.
Chung-Lin Lee, et al. Diagnostics (Basel, Switzerland) 2024 0 (8) - The risk of pediatric cardiovascular diseases in offspring born to mothers with systemic lupus erythematosus: a nationwide study.
Jong Ho Cha, et al. Frontiers in pediatrics 2023 0 1294823 - Whole-exome sequencing analysis of patent ductus arteriosus in a Japanese macaque (Macaca fuscata).
Young-Jin Jang, et al. Journal of medical primatology 2023 0 - Etiology and prognosis of nephrocalcinosis according to gestational age in Korean children.
Jinwoon Joung, et al. BMC pediatrics 2023 0 (1) 451 - Association of the EPAS1 rs7557402 Polymorphism with Hemodynamically Significant Patent Ductus Arteriosus Closure Failure in Premature Newborns under Pharmacological Treatment with Ibuprofen.
Diana G Rogel-Ayala, et al. Diagnostics (Basel, Switzerland) 2023 0 (15) - Early neurodevelopmental outcomes of extreme preterm infants exposed to paracetamol: a retrospective cohort study.
Bella Zhong, et al. Pediatric research 2023 0 1-6 - Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome.
Lin Yunting, et al. Frontiers in genetics 2023 0 1085210
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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
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