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2,973 Possible Causes for Abnormal Corticomedullary Differentiation, female gonadal dysgenesis, Pyoureter

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

  • Hydronephrosis

    In Gardner-Silengo-Wachtel syndrome (Micrognathia, low set ears, double outlet right ventricle with VSD and 46 XY Gonadal dysgenesis). No polydactyly.[] Perinephric urinoma Keyhole sign Loss of renal parenchyma, as suggested by: (i) cortical thinning, (ii) poor corticomedullary differentiation, (iii) increased renal echogenicity[] High association with other congenital anomalies such as imperforate anus, cardiac problems, Turner Syndrome, VACTERL association, cerebral and lumbo- sacral abnormalities[]

  • Benign Papilloma of the Ureter

    Return to top MALE GU SEX DISORDERS: GENETIC SEX TURNER SYNDROME : XO genotype. MIXED GONADAL DYSGENESIS : 1 defined gonad plus a contralateral streak gonad.[] EPIDEMIOLOGY / PATHOGENESIS: Almost exclusively seen in patients with some form of gonadal dysgenesis (testicular feminization).[] SYMPTOMS: Four-fifths of patients with gonadoblastomas are phenotypic females. Males typically have cryptorchidism or hypospadias.[]

    Missing: Abnormal Corticomedullary Differentiation
  • Acute Pyelonephritis

    Acute pyelonephritis is not considered a common cause of renal vein (RVT) and inferior vena caval thrombosis (IVCT). Apart from malignancy, RVT is not an uncommon condition amongst patients with nephrotic syndrome, most commonly seen in patients with membranous glomerulonephritis. However, RVT occurring in[…][]

    Missing: Abnormal Corticomedullary Differentiation female gonadal dysgenesis
  • Ureterolithiasis

    OBJECTIVE: The tissue rim sign-a rim or halo of soft-tissue attenuation seen around the circumference of an intraureteral calculus on unenhanced axial CT-has been described as useful in differentiating ureteral calculi from extraurinary abdominal or pelvic calcifications. The purpose of this study was to determine[…][]

    Missing: Abnormal Corticomedullary Differentiation female gonadal dysgenesis
  • Hypertrichotic Osteochondrodysplasia

    syndrome 15 cases 1479 defects 11 cases3459 Absence of fingerprints - congenital milia 14 cases Cooks syndrome1658 ADULT syndrome 14 cases 1487 Familial acute necrotizing[] *impetigo 【膿眼】*pyophthalmia *pyophthalmitis 【膿気胸】*pyopneumothorax 【膿形成】*pyogenesis *pyopoiesis ( 化膿) 【膿血症】*pyemia 【膿腎症】*pyonephrosis 【膿精液症】*pyospermia 【膿瘡】*ecthyma 【膿尿管】*pyoureter[] […] of cardiovascular system morphology Abnormality of the dentition Short nose Blindness Dysplastic tricuspid valve Abnormality of the umbilicus Reduced renal corticomedullary[]

  • Growth Failure

    There were six females, seven males, and one patient with gonadal dysgenesis. All were prepuberal and were under care of one[] Syndrome. 1 Growth failure due to Turner Syndrome, which affects approximately 1:2,000 girls, is a genetic defect in which all or part of one of the two X-chromosomes is[] In the presented case all the typical phenotypic stigmata related to Turner syndrome were missing.[]

    Missing: Abnormal Corticomedullary Differentiation Pyoureter
  • Chronic Pyelonephritis

    Vesicoureteral reflux and chronic pyelonephritis are usually associated with proteinuria of less than 1 gm. per 24 hours. When there is massive proteinuria an associated glomerulopathy is usually present. We describe a patient who had nephrotic syndrome with radiological evidence of ureterovesical reflux and[…][]

    Missing: Abnormal Corticomedullary Differentiation female gonadal dysgenesis
  • Ureteral Stricture

    To present our technique of ureteral replacement with an appendicovesicostomy for the treatment of extended ureteral stricture after kidney transplantation. Ureteral stricture represents a urologic complication that may cause progressive function impairment and graft loss. Symptomatic ureteral stenosis is[…][]

    Missing: Abnormal Corticomedullary Differentiation female gonadal dysgenesis
  • Hypogonadism

    (primary hypogonadism) in females include the following: Turner syndrome Inactivating mutations XX and XY gonadal dysgenesis Premature menopause Radiation therapy Chemotherapy[] Congenital causes include the following:[1][3][4] Chromosomal abnormalities (resulting in gonadal dysgenesis) - Turner's syndrome, Klinefelter's syndrome, Swyer's syndrome[] Turnerâ s syndrome is also called monosomy X, gonadal dysgenesis, or Bonnevie-Ullrich syndrome. Children with hypogonadism do not enter puberty.[]

    Missing: Abnormal Corticomedullary Differentiation Pyoureter
  • Gonadoblastoma

    We report two female patients with gonadal dysgenesis and sex chromosome mosaicism involving the Y chromosome.[] Gonadoblastoma is an uncommon ovarian tumor arising primarily in females with gonadal dysgenesis and a 46, XY karyotype.[] Gonadoblastoma, a rare gonadal neoplasm, is composed of germ cells and sex cord derivatives and usually occurs in phenotypically female patients with gonadal dysgenesis.[]

    Missing: Abnormal Corticomedullary Differentiation Pyoureter

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