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Medical condition
Hyperoxaluria is an excessive urinary excretion of oxalate. Individuals with hyperoxaluria often have calcium oxalate kidney stones. It is sometimes called
Hyperoxaluria
Medical condition
Primary hyperoxaluria is a rare condition (autosomal recessive) resulting in increased excretion of oxalate (up to 600 mg a day from normal 50 mg a day)
Primary_hyperoxaluria
Medication
brand name Rivfloza, is a medication used for the treatment of primary hyperoxaluria. It is an LDHA-directed small interfering RNA developed by Dicerna Pharmaceuticals
Nedosiran
Species of bacterium
role in mitigating calcium oxalate kidney stone disease and primary hyperoxaluria because it metabolizes oxalate as its primary carbon source. In vitro
Oxalobacter_formigenes
Medication for the treatment of primary hyperoxaluria type 1
the brand name Oxlumo, is a medication for the treatment of primary hyperoxaluria type 1 (PH1). The most common side effects include injection site reactions
Lumasiran
Any derivative of oxalic acid; chemical compound containing oxalate moiety
termed hyperoxalemia, and high levels of oxalate in the urine is termed hyperoxaluria. Although unusual, consumption of oxalates (for example, the grazing
Oxalate
Purplish discoloration of the skin due to reduced blood flow
facial dysmorphism, immunodeficiency, livedo, and short stature) Primary hyperoxaluria, oxalosis (oxalate vasculopathy) Cytomegalovirus infection (very rare
Livedo_reticularis
Simplest dicarboxylic acid. (COOH)2
Rhubarb Compendium) Oxalosis & Hyperoxaluria Foundation (OHF) The Oxalate Content of Food 2008 (PDF) Oxalosis & Hyperoxaluria Foundation (OHF) Diet Information
Oxalic_acid
Formation of mineral deposits in the kidneys
renal tubular acidosis, Dent's disease, hyperparathyroidism, primary hyperoxaluria, or medullary sponge kidney. 3–20% of people who form kidney stones
Kidney_stone_disease
Protein-coding gene in humans
alter subcellular targeting, have been associated with type I primary hyperoxaluria. Peroxisomal disorder GRCh38: Ensembl release 89: ENSG00000172482 –
AGXT
Type of inflammatory bowel disease
calcium oxalate or uric acid stones. Calcium oxalate stones due to hyperoxaluria are typically associated with either distal ileal Crohn's disease or
Crohn's_disease
Medical condition caused by the deposition of calcium salts in the kidneys
syndrome, acute phosphate nephropathy, and occasional cases of enteric hyperoxaluria. Nephrocalcinosis is connected with conditions that cause hypercalcaemia
Nephrocalcinosis
Autoimmune disorder
B12. Vitamin D deficiency can cause secondary hyperparathyroidism. Hyperoxaluria and kidney stones can be caused by malabsorption of fats, and peptides
Coeliac_disease
Red raspberry
roots of R. idaeus prevented kidney stone formation in a mouse model of hyperoxaluria. Tiliroside from raspberry is a potent tyrosinase inhibitor and might
Rubus_idaeus
Acetic acid bearing an aldehyde group
early predictive marker. Glyoxylate is involved in the development of hyperoxaluria, a key cause of nephrolithiasis (commonly known as kidney stones). Glyoxylate
Glyoxylic_acid
Chemical compound
liver-targeted molecule and is being investigated for the treatment of primary hyperoxaluria. By inhibiting the final and only committed step in hepatic oxalate
CHK-336
Human chromosome
Beta-centractin AGXT: alanine-glyoxylate aminotransferase (oxalosis I; hyperoxaluria I; glycolicaciduria; serine-pyruvate aminotransferase) ALS2: amyotrophic
Chromosome_2
Biological molecules constituting nucleic acids
lateral sclerosis, homozygous familial hypercholesterolemia, and primary hyperoxaluria type 1 are all amenable to ASO-based therapy. The application of oligonucleotides
Nucleotide
Protein-coding gene in the species Homo sapiens
widespread tissue expression and has a role in metabolism. Type II hyperoxaluria is caused by mutations in this gene. GRHPR mutation analysis needs to
GRHPR
Protein-coding gene in the species Homo sapiens
urine, predisposing to oxalate stone; a condition known as primary hyperoxaluria type III. GRCh38: Ensembl release 89: ENSG00000241935 – Ensembl, May
HOGA1
disease Miglustat Nedosiran To lower urinary oxalate levels in primary hyperoxaluria type 1 and relatively preserved kidney function Nirogacestat To treat
List of drugs granted breakthrough therapy designation
List_of_drugs_granted_breakthrough_therapy_designation
Hutchinson–Gilford progeria syndrome LMNA 1:18,000,000 Hyperlysinemia AASS recessive Hyperoxaluria, primary AGXT, GRHPR, DHDPSL Hyperphenylalaninemia 12q Hypoalphalipoproteinemia
List_of_genetic_disorders
neonatal MeSH C18.452.429.500 – kernicterus MeSH C18.452.497.490 – hyperoxaluria, primary MeSH C18.452.565.100 – anemia, iron-deficiency MeSH C18.452
List_of_MeSH_codes_(C18)
Human chromosome
(NPS) nonsyndromic deafness OCD polycythemia vera porphyria primary hyperoxaluria STXBP1 Tangier disease tetrasomy 9p thrombotic thrombocytopenic purpura
Chromosome_9
Natural regrowth of damaged liver tissue
duct cancer), genetic disorders (hemochromatosis, Wilson's disease, hyperoxaluria). The liver is a critical organ that is responsible for many different
Liver_regeneration
Type of enzyme
Molecule Inhibitor of Lactate Dehydrogenase for the Treatment of Primary Hyperoxaluria: PO1620". Journal of the American Society of Nephrology. 31 (10S): 514
Lactate_dehydrogenase_A
Enzyme
caused by a rare inherited autosomal recessive disorder known as primary hyperoxaluria type II (PH2). This condition can cause nephrolithiasis (kidney stone)
Glyoxylate_reductase
Medical condition
Pipecolic acidemia 600964 PHYH E80.301 Acatalasia 115500 CAT E80.310 Hyperoxaluria type 1 259900 AGXT E80.311 Acyl-CoA oxidase deficiency 264470 ACOX1
Peroxisomal_disorder
corticalis generalisata Hyperostosis frontalis interna Hyperoxaluria type 1 Hyperoxaluria type 2 Hyperoxaluria Hyperparathyroidism Hyperparathyroidism, familial
List_of_diseases_(H)
Biological process of gene regulation
United States. This medication is used for the treatment of primary hyperoxaluria type 1 (PH1) in pediatric and adult populations. The drug is designed
RNA_interference
Process
Liver-Targeted, Small Molecule Lactate Dehydrogenase Inhibitor for Hyperoxaluria Treatment". Journal of the American Society of Nephrology. doi:10.1681/ASN
Target-mediated drug disposition
Target-mediated_drug_disposition
Class of membrane transport proteins
GLUT1 deficiency syndrome, cystic fibrosis, Hartnup disease, primary hyperoxaluria and hypokalemic periodic paralysis. The glucose transporter (GLUTs)
Uniporter
than that of LDH so the production of glycolate is dominant. Primary hyperoxaluria is a condition that results in the overproduction of oxalate which combines
Glycerate_dehydrogenase
German-born American general surgeon and transplant surgeon
"Preemptive Liver Transplantation from a Living Related Donor for Primary Hyperoxaluria Type I". New England Journal of Medicine. 338 (26): 1924. doi:10
Rainer_Gruessner
Medical condition
with L-Glyceric acidemia (a.k.a. L-glyceric aciduria, a.k.a. primary hyperoxaluria type II), which is associated with mutations in the GRHPR (encoding
D-Glyceric_acidemia
American gene editing company
hypercholesterolemia, and PBGENE-PH1, a candidate to treat primary hyperoxaluria type 1. Precision is in the process of developing multiple candidates
Precision_BioSciences
Medical condition
stone analysis. Differential diagnosis Uric acid nephrolithiasis, Xanthinuria, and Primary hyperoxaluria. Medication Allopurinol. Frequency 0.4% to 1.2%
Adenine phosphoribosyltransferase deficiency
Adenine_phosphoribosyltransferase_deficiency
Medical condition
purpura can be seen in opportunistic infections, calciphylaxis, primary hyperoxaluria, livedoid vasculopathy, pyoderma gangrenosum, and vasculopathy or vasculitis
Retiform_purpura
Medical condition
HSPB5) FLNC (filamin C) Infiltrative Amyloidosis Sarcoidosis Primary hyperoxaluria Storage diseases Fabry disease Gaucher disease Hereditary hemochromatosis
Restrictive_cardiomyopathy
old liver tissue obtained from a 9-year-old male patient with primary hyperoxaluria (after the approval of ethical committee and required written consent)
HuS-E/2_cells
Consumption or injection of very large doses of vitamin C
test. Because oxalic acid is produced during metabolism of vitamin C, hyperoxaluria can be caused by intravenous administration of ascorbic acid. Vitamin
Vitamin_C_megadosage
Primary cutaneous amyloidosis Primary granulocytic sarcoma Primary hyperoxaluria Primary hyperparathyroidism Primary lateral sclerosis Primary malignant
List_of_diseases_(P)
Chemical compound
kidney stone formation is inhibited, making it a good treatment for hyperoxaluria (a condition in which there is excessive oxalate excretion in the urine
Khellin
Protein-coding gene in the species Homo sapiens
1016/j.abb.2007.06.021. PMID 17669354. Danpure CJ (2005). "Primary hyperoxaluria: From gene defects to designer drugs?". Nephrology Dialysis Transplantation
Hydroxyacid oxidase (glycolate oxidase) 1
Hydroxyacid_oxidase_(glycolate_oxidase)_1
New Zealand crystallographer (1927–1990)
Hermon Dowling, R.; Rose, G. Alan; June Sutor, D. (29 May 1971). "Hyperoxaluria and Renal Calculi in Ileal Disease". The Lancet. Originally published
June_Sutor
Protein-coding gene in humans
1152/ajpcell.00238.2004. PMID 15240345. Danpure CJ (August 2005). "Primary hyperoxaluria: from gene defects to designer drugs?". Nephrology, Dialysis, Transplantation
AGXT2
Species of bacterium
roles in mitigating calcium oxalate kidney stone disease and primary hyperoxaluria because of its unique ability to utilize oxalate as its primary carbon
Oxalobacter_aliiformigenes
Type of surgery for treating obesity
risk of the intestinal bypass surgery. This is mainly due to enteric hyperoxaluria. Increased absorption of oxalate in colons rises the risk of the formation
Intestinal_bypass
US Food and Drug Administration drug review program
muscular dystrophy Sarepta Therapeutics 2020 Rare pediatric Oxlumo Primary hyperoxaluria type 1 Alnylam Pharmaceuticals 2020 Rare pediatric Rethymic Congenital
Priority_review
endosteal; 144750; LRP5 Hyperoxaluria, primary, type 1; 259900; AGXT Hyperoxaluria, primary, type II; 260000; GRHPR Hyperoxaluria, primary, type III; 613616;
List_of_OMIM_disorder_codes
Surgical weight-loss procedure
coincide in bowel-associated dermatosis-arthritis syndrome. Renal disease: Hyperoxaluria, with oxalate stones or interstitial oxalate deposits, immune complex
Jejunoileal_bypass
Medical conditions
PMID 17578801. S2CID 25201041. McDonald GB, Earnest DL, Admirand WH (1977). "Hyperoxaluria correlates with fat malabsorption in patients with sprue". Gut. 18 (7):
Gluten-sensitive enteropathy–associated conditions
Gluten-sensitive_enteropathy–associated_conditions
syndrome MeSH C12.777.419.307 – hydronephrosis MeSH C12.777.419.320 – hyperoxaluria, primary MeSH C12.777.419.331 – hypertension, renal MeSH C12.777.419
List_of_MeSH_codes_(C12)
chocolate, rhubarb, spinach, dark green vegetables, fruits) can help reduce hyperoxaluria (excessive urinary excretion of oxalate). Reducing the amount of meats
Renal stone formation in space
Renal_stone_formation_in_space
620 – glycogen storage disease type VIII MeSH C16.320.565.202.460 – hyperoxaluria, primary MeSH C16.320.565.202.589 – lactose intolerance MeSH C16.320
List_of_MeSH_codes_(C16)
HYPEROXALURIA
HYPEROXALURIA
HYPEROXALURIA
HYPEROXALURIA
Girl/Female
Tamil
Sreelaya | à®·à¯à®°à¯€à®²à®¾à®¯à®¾
Girl/Female
Arabic, Muslim
Name of a Sahabiyah (RA)
Boy/Male
British, English
From the Sword Meadow
Boy/Male
Indian
Certain
Girl/Female
Arabic, Muslim
Nightingale; Plural of Andalib
Boy/Male
Indian, Tamil
One who Wins the Wealth
Boy/Male
English
Gentle. Famous Bearer: Clement Moore, writer of 'Twas the Night Before Christmas'.
Boy/Male
Muslim
Angel, Guard of paradise, Bringer of good news (1)
Girl/Female
Hindu
Goddess Durga, Red in color
Biblical
a name applied to those who are born by Caesarean section
HYPEROXALURIA
HYPEROXALURIA
HYPEROXALURIA
HYPEROXALURIA
HYPEROXALURIA