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3,546 Possible Causes for Abnormal Corticomedullary Differentiation, female gonadal dysgenesis, Magnesium Decreased

Did you mean: Abnormal Corticomedullary Differentiation, female, gonadal dysgenesis, Magnesium Decreased

  • 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[]

  • Osteopetrosis

    dysgenesis) GnRHR (Gonadotropin-releasing hormone insensitivity) EDNRB (ABCD syndrome, Waardenburg syndrome 4a, Hirschsprung's disease 2) AVPR2 (Nephrogenic diabetes insipidus[] Normal corticomedullary differentiation was evident in five (P   0.06) and 12 (P   0.005) patients at 6 and 12 months, respectively.[] […] hypothyroidism 1) LHCGR (Luteinizing hormone insensitivity, Leydig cell hypoplasia, Male-limited precocious puberty) FSHR (Follicle-stimulating hormone insensitivity, XX gonadal[]

  • Diabetes Mellitus

    These include the chromosomal abnormalities of Down’s syndrome, Klinefelter’s syndrome, and Turner’s syndrome.[] […] risk of developing T2D. 4, 5, 41, 42 In addition, higher magnesium intake has been consistently associated with reduced risk of T2D in cohort studies or improved glucose[] Other Genetic Diseases Diabetes occurs in people with Down syndrome, Klinefelter syndrome, and Turner syndrome at higher rates than the general population.[]

    Missing: Abnormal Corticomedullary Differentiation
  • Celiac Disease

    syndrome, Williams syndrome, selective immunoglobulin (Ig)A deficiency and first degree relatives of individuals with celiac disease.[] […] dental enamel defects, osteoporosis, short stature, delayed puberty and persistent iron deficiency anemia and in asymptomatic individuals with type 1 diabetes, Down syndrome, Turner[]

    Missing: Abnormal Corticomedullary Differentiation
  • Growth Failure

    There were six females, seven males, and one patient with gonadal dysgenesis. All were prepuberal and were under care of one[] We also observed some findings that suggested chronic hypovolemia (decreased total blood volume), namely increased calcium (5 out of 10) and magnesium (4 out of 10) levels[] 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[]

    Missing: Abnormal Corticomedullary Differentiation
  • Inflammatory Bowel Disease Type 1

    Turner's syndrome associated with chronic inflammatory bowel disease. A case report and review of the literature.[] […] of anti-lithogenic substances as citrate and magnesium.[] ’s syndrome[ 32 ], and congenital[ 33 ], cyclic[ 34 ] and autoimmune[ 35 ] neutropenias can all manifest features of CD or CD-like phenotype[ 36 ].[]

    Missing: Abnormal Corticomedullary Differentiation
  • Graves Disease

    Two (2) patients had Turner syndrome, another one (1), diabetic, was on insulin therapy.[]

    Missing: Abnormal Corticomedullary Differentiation
  • Malabsorption Syndrome

    syndrome  lactose intolerance  intestinal cancer  intestinal lymphoma 40.  The triggers for CD are specific immunogenic peptides that are present only and exclusively[] Mechanisms include rapid gut transit, decreased activity of intestinal disaccharidases, and decreased pancreatic function 21 Drugs.[] […] with celiac include:  rheumatoid arthritis  type 1 diabetes  thyroid disease  autoimmune liver disease  Addison’s disease  Sjogren’s disease  lupus  Down syndrome  Turner[]

    Missing: Abnormal Corticomedullary Differentiation
  • Proximal Renal Tubular Acidosis

    The transcript of the SLC4A4 gene was almost undetectable, and the patient was also diagnosed with Turner's syndrome.[]

    Missing: Abnormal Corticomedullary Differentiation
  • Hypoparathyroidism

    Gonadal dysgenesis. As part of an autoimmune process: [ 3 ] Autoimmune polyglandular syndrome type 1 (APS-1): autosomal recessive inheritance.[] When ca is up this is down and vice versa phosophorus and magnesium If PTH is decreased it is because there is not enough calcium Undersecretion of the parathyroid hormone[] Results also indicated that serum calcium remained stable and 24-hour urinary calcium decreased by 32%.[]

    Missing: Abnormal Corticomedullary Differentiation

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