Splenomegaly
What's New
Last Posted: Nov 17, 2022
- Targeted Screening for Gaucher Disease in High Suspicion Patients and Clinical Profile of Screen Positives in a Large Pediatric Multispecialty Hospital.
Magar Suvarna et al. Cureus 2022 14(10) e29868 - Spleen size in homozygous sickle cell disease: TRENDS in a birth cohort using ultrasound.
Walker Thomas M et al. The British journal of radiology 2022 20220634 - Stroke Prevention with Hydroxyurea Enabled through Research and Education (SPHERE): a Phase 2 primary stroke prevention trial in sub-Saharan Africa.
Smart Luke R et al. Acta haematologica 2022 - A study of spectrum of sickle cell anemia and thalassemia in a teaching institute of South India.
Sabitha Rani S S et al. Nigerian journal of clinical practice 2022 25(4) 490-495 - Influence of diabetes and hypercholesterolemia on laboratory methods for hereditary spherocytosis diagnosis.
Lazarova Elena et al. Journal of clinical laboratory analysis 2022 e24248 - Manifestations of HbSE sickle cell disease: a systematic review.
Khamees Ibrahim et al. Journal of translational medicine 2021 19(1) 262 - Gene Therapy for Mucopolysaccharidosis Type II-A Review of the Current Possibilities.
Zapolnik Pawel et al. International journal of molecular sciences 2021 22(11) - Newborn Screening Practices and Alpha-Thalassemia Detection - United States, 2016.
Bender M A et al. MMWR. Morbidity and mortality weekly report 2020 Sep 69(36) 1269-1272 - Clinical and genetic characteristics of autosomal recessive polycystic kidney disease in Oman.
Al Alawi Intisar et al. BMC nephrology 2020 Aug 21(1) 347 - Homozygous sickle cell disease in Central India & Jamaica: A comparison of newborn cohorts.
Jain Dipty et al. The Indian journal of medical research 2020 Apr 151(4) 326-332
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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
- Page last updated:Apr 21, 2024
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