Renal Tubular Acidosis
What's New
Last Posted: Feb 19, 2020
- Genetic Testing in Pediatric Kidney Disease.
Arora Veronica et al. Indian journal of pediatrics 2020 Feb - Treatment and long-term outcome in primary distal renal tubular acidosis.
Lopez-Garcia Sergio Camilo et al. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2019 Feb - Genotype-Phenotype Analysis in Pediatric Patients with Distal Renal Tubular Acidosis.
Park Eujin et al. Kidney & blood pressure research 2018 Mar 43(2) 513-521 - Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.
Ashton Emma J et al. Kidney international 2018 Feb - Distal renal tubular acidosis with hemolytic anemia
From NCATS Genetic and Rare Diseases Information Center - Neuroaxonal dystrophy renal tubular acidosis
From NCATS Genetic and Rare Diseases Information Center - Renal tubular acidosis
From NCATS Genetic and Rare Diseases Information Center - Renal tubular acidosis with deafness
From NCATS Genetic and Rare Diseases Information Center - Renal tubular acidosis, distal
From NCATS Genetic and Rare Diseases Information Center - Renal tubular acidosis, distal, autosomal dominant
From NCATS Genetic and Rare Diseases Information Center
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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 01, 2024
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