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27 Possible Causes for Abnormal Corticomedullary Differentiation, female gonadal dysgenesis, Nephrolithiasis

Did you mean: Abnormal Corticomedullary Differentiation, female, gonadal dysgenesis, Nephrolithiasis

  • Hydronephrosis

    In Gardner-Silengo-Wachtel syndrome (Micrognathia, low set ears, double outlet right ventricle with VSD and 46 XY Gonadal dysgenesis). No polydactyly.[omicsonline.org] Hydronephrosis; Chronic hydronephrosis; Acute hydronephrosis; Urinary obstruction; Unilateral hydronephrosis; Nephrolithiasis - hydronephrosis; Kidney stone - hydronephrosis[nlm.nih.gov] Perinephric urinoma Keyhole sign Loss of renal parenchyma, as suggested by: (i) cortical thinning, (ii) poor corticomedullary differentiation, (iii) increased renal echogenicity[indianpediatrics.net]

  • Congenital Hydronephrosis

    In Gardner-Silengo-Wachtel syndrome (Micrognathia, low set ears, double outlet right ventricle with VSD and 46 XY Gonadal dysgenesis). No polydactyly.[omicsonline.org] Acute upper tract obstruction [ 6 ] See also separate Urinary Tract Stones (Nephrolithiasis) article.[patient.info] Perinephric urinoma Keyhole sign Loss of renal parenchyma, as suggested by: (i) cortical thinning, (ii) poor corticomedullary differentiation, (iii) increased renal echogenicity[indianpediatrics.net]

  • Tumor Lysis Syndrome

    Another common feature of Turner syndrome is the failure of the ovaries to develop properly (gonadal dysgenesis).[rarediseases.org] Two common conditions related to excess uric acid, gout and uric acid nephrolithiasis, are not features of tumor lysis syndrome.[en.wikipedia.org] The ultrasonographic image on the right shows a kidney from a patient with the tumor lysis syndrome, in which there is loss of the normal corticomedullary differentiation[ncbi.nlm.nih.gov]

  • Fanconi Renotubular Syndrome

    dysgenesis, trisomy X * Thymus in DiGeorge syndrome * Labia majora in popliteal pterygium syndrome * Corpus callosum, connecting the two sides of the brain, in Agenesis of[dbpedia.org] Table 1 Nephrolithiasis associated with inborn metabolic diseases according to presentation and pathophysiology Nephrolithiasis associated with inborn metabolic diseases have[doi.org] Abdominal ultrasound showed kidneys measuring 146 mm with preserved corticomedullary differentiation and no signs of hydronephrosis.[revistanefrologia.com]

  • Medullary Cystic Kidney Disease

    […] one - 1:750 Usually at inferior pole - 90% Most common congenital renal defect Located in lower abdo usually gets hooked on inferior mesenteric artery when ascending Assoc Turner[alancam.com] , occur due to dilatation of terminal part of collecting ducts (duct of Balani) that present as hematuria, urinary infection, distal renal tubular acidosis (RTA), and/or nephrolithiasis[gradestack.com] Histological examination usually reveals abnormalities in ductal differentiation and minimal corticomedullary differentiation.[lecturio.com]

  • Mulibrey Nanism Syndrome

    Syndrome 17 Hermaphroditism True 139 Von HippelLindau Disease 18 Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism[books.google.de] , type I; 310468; CLCN5 Nephrolithiasis/osteoporosis, hypophosphatemic, 1; 612286; SLC34A1 Nephrolithiasis/osteoporosis, hypophosphatemic, 2; 612287; SLC9A3R1 Nephronophthisis[howlingpixel.com] […] disease in the right kidney, such as poor corticomedullary differentiation and cortical atrophy that were confirmed by renal scintigraphy (Fig. 3 ).[academic.oup.com]

  • Waters-West Syndrome

    Turner syndrome: Turner syndrome, Macro, autopsy (73731) Turner syndrome, Macro, autopsy (73732) Turner syndrome, Macro, autopsy (73733) Turner syndrome, Macro, autopsy ([atlases.muni.cz] , Calcium Oxalate 2 Nephrolithiasis/Osteoporosis, Hypophosphatemic, 1 1 Nephrolithiasis/Osteoporosis, Hypophosphatemic, 2 2 Nephronophthisis 3 Nephronophthisis 11 3 Nephronophthisis[preventiongenetics.com] […] atrophy Adrenal insufficiency Absence of renal corticomedullary differentiation Hemolytic anemia Ptosis Lethargy Pachygyria Heterotopia Decreased liver function Aspiration[mendelian.co]

  • Mazabraud Syndrome

    Effects of recombinant human growth hormone on height in Turner syndrome .; 生长激素对Turner综合征的促身高作用 3.[dictall.com] Dents disease • Cause of Fanconi syndrome • Proteinuria • Hypercalcuria nephrocalcinosis • Nephrolithiasis 58.[de.slideshare.net] differentiation, being replaced classically by a homogeneous ground glass appearance, although mixed lucencies and sclerosis are also common 2-4 .[radiopaedia.org]

  • Familial Juvenile Hyperuricemic Nephropathy Type 2

    Syndrome 17 Hermaphroditism True 139 Von HippelLindau Disease 18 Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism[books.google.de] Ausgewählte Seiten Seite 15 Seite 33 Seite 30 Seite 37 Seite 16 Inhalt An Overview 1 Chapter 2 Uric Acid Metabolism in Health 9 Chapter 3 Uric Acidassociated Nephropathies and Nephrolithiasis[books.google.de] Kidney size is either normal or reduced in MCKD, and ultrasound demonstrates increased echogenicity, loss of corticomedullary differentiation, and medullary cysts ( Figure[renalandurologynews.com]

  • Congenital Hemihypertrophy

    Array-CGH analysis in patients with syndromic and non-syndromic XY gonadal dysgenesis: evaluation of array CGH as diagnostic tool and search for new candidate loci.[richtlijnendatabase.nl] A case of medullary sponge kidney associated with congenital hemihypertrophy, complicated by nephrocalcinosis and nephrolithiasis, is reported here.[ncbi.nlm.nih.gov] Heterogeneous Growth delay Respiratory distress Meningoencephalocele Episodic tachypnea Absence of renal corticomedullary differentiation Brainstem dysplasia Neonatal breathing[mendelian.co]

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