Autosomal Dominant Polycystic Kidney Disease
Autosomal Dominant Polycystic Kidney Disease: Review and Management Update
... Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited ...mainly polycystic liver disease and cerebral aneurysms, which contribute to increased ...
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Caffeine intake by patients with autosomal dominant polycystic kidney disease
... and kidney enlargement in autosomal dominant polycystic kidney disease (ADPKD), we evaluated caffeine intake and renal volume using renal ultrasound in ADPKD ...chronic ...
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Cyst infection in hospital-admitted autosomal dominant polycystic kidney disease patients is predominantly multifocal and associated with kidney and liver volume
... in autosomal dominant polycystic kidney disease ...of kidney and/or liver involvement, however, remain ...in kidney (KCI) and liver (LCI) in ...Total kidney (TKV) ...
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Renal and extrarenal manifestations of autosomal dominant polycystic kidney disease
... and kidney size (16,17) have been identified as risk factors that might influence a faster progression to ...cystic disease is related to the earlier occurrence of renal insufficiency ...
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Radiologic and clinical bronchiectasis associated with autosomal dominant polycystic kidney disease.
... A proposed mechanism for the development of bronchiectasis in patients with ADPKD may be linked to abnormalities in polycystin-1 and 2, the gene products of PKD1 and PKD 2 located on chromosomes 16 and 4 respectively. ...
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Pain determinants of pain in autosomal dominant polycystic kidney disease
... Pain is the most common symptom re- ported by ADPKD patients, afflicting approximately 60% of cases and may result from renal hemorrhage, calculi, urinary tract infections, cyst rupture, or due to stretching of the ...
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Nitric oxide synthase and polycystic kidney disease
... Endothelial nitric oxide plays a crucial role in the control of local hemodynamics and systemic blood pressure. Thus, it has been proposed that gene coding for endothelial nitric oxide synthase (eNOS) could have a ...
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Rev. Assoc. Med. Bras. vol.60 número3
... Does ultrasound examination allow confirming the clinical diagnosis of autosomal dominant polycystic kidney disease (ADPKD)a. Patients aged over 60 years with 4 or more cysts in.[r] ...
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Int. braz j urol. vol.33 número1
... symptomatic autosomal dominant polycystic kidney ...massive polycystic kidneys with a kidney volume of greater than 3,500 cc are at increased risk for open conversion and they ...
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ISSN 0100-879X BIOMEDICAL SCIENCES AND CLINICAL INVESTIGATION
... Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common human life-threatening monogenic disor- ...The disease is characterized by bilateral, progressive ...
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Camundongos com deficiência em Pkd1 apresentam disfunção cardíaca, fenótipo atenuado...
... Renal volume, renin-angiotensin-aldosterone system, hypertension, and left ventricular hypertrophy in patients with autosomal dominant polycystic kidney disease. Schroen B, Heymans S, [r] ...
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Surface glycosylation profiles of urine extracellular vesicles.
... with autosomal dominant polycystic kidney disease to those of age-matched ...of polycystic kidney disease and healthy uEVs showed differences in binding intensity ...
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Clinics vol.61 número6
... huge autosomal dominant polycystic kidney disease usually have an umbilical hernia and rectus abdominis diastasis, which are very ...
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Aneurisma gigante do segmento intracavernoso da carótida interna associado a doença renal policística autossômica dominante: relato de caso.
... ABSTRACT - We report the case of a 60 years-old woman with autosomal dominant polycystic kidney disease (ADPKD) that presented with headache and right complete ophthalmoplegia. The CT ...
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O crescimento cístico renal é o principal determinante para o desenvolvimento de...
... in autosomal dominant polycystic kidney disease (ADPKD) patients compared with the general population, being present in ~60% of affected individuals before the loss of renal ...
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Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation.
... Direct DNA sequencing identified 8 possible disease-causing mutations among 20 autosomal dominant families (Table 1). There were one deletion mutation (c.211delC), one insertion mutation ...
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Steviol reduces MDCK Cyst formation and growth by inhibiting CFTR channel activity and promoting proteasome-mediated CFTR degradation.
... in polycystic kidney disease (PKD) involves cAMP-activated proliferation of cyst-lining epithelial cells and transepithelial fluid secretion into the cyst lumen via cystic fibrosis transmembrane ...
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Striatal and extrastriatal atrophy in Huntington’s disease and its relationship with length of the CAG repeat
... We report the minimum, maximum and mean values and SD for the volumes of the structures analyzed, and P values less than 0.05 were accepted as statistically signifi- cant. We used analysis of variance (ANOVA) to compare ...
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Int. braz j urol. vol.31 número6
... an autosomal dominant disease, charac- terized by multiple bilateral renal cysts, nonfunctioning and ...the kidney will be transplanted, or due to hypertension or refractory pain, hematuria ...
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Rev. bras.oftalmol. vol.75 número1
... a disease of dominant autosomal inheritance, is characterized by dysphagia, paresis of the extraocular muscles, proximal paresis of the extremities and progressive bilateral ptosis, forcing the ...
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