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3,709 Possible Causes for Abnormal Corticomedullary Differentiation, female gonadal dysgenesis, Phosphate Decreased

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

  • Osteopetrosis

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

  • Celiac Disease

    syndrome, Williams syndrome, selective immunoglobulin (Ig)A deficiency and first degree relatives of individuals with celiac disease.[ncbi.nlm.nih.gov] […] albumin level Malnutrition Elevated calcium level, decreased phosphate level Vitamin D deficiency, secondary hyperparathyroidism Thrombocytosis, leukocytosis General inflammatory[aafp.org] […] dental enamel defects, osteoporosis, short stature, delayed puberty and persistent iron deficiency anemia and in asymptomatic individuals with type 1 diabetes, Down syndrome, Turner[ncbi.nlm.nih.gov]

    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[jamanetwork.com] This process can decrease blood phosphorus levels and increase blood calcium levels. Phosphate binders come as chewable tablets, liquids, capsules, and pills.[my.clevelandclinic.org] 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[hcp.merckgroup.com]

    Missing: Abnormal Corticomedullary Differentiation
  • Childhood Celiac Disease

    syndrome Williams syndrome A relative with celiac disease[gikids.org] Turner Syndrome and Celiac Disease: A Case-Control Study. Pediatrics. 2016 Feb. 137 (2):e20152232. [Medline]. Osterweil N.[emedicine.medscape.com] syndrome and selective IgA deficiency, as well as those with first-degree relatives with CD.[glutenfreetherapeutics.com]

    Missing: Abnormal Corticomedullary Differentiation
  • Malignant Melanoma

    Syndrome 03 Oct 1995 Ed Jennings Cleared of All Charges 13 Sep 1995 Genentech Completes Negotiations, Purchases Land For New Manufacturing Facility in Vacaville, CA 21 Aug[gene.com] Earnings for Third Quarter 1995 05 Oct 1995 Genentech's Blood Platelet Factor (TPO) Enters the Clinic as Phase I Trial Begins 04 Oct 1995 Genentech Submits NDA for Nutropin in Turner's[gene.com]

    Missing: Abnormal Corticomedullary Differentiation
  • Anterior Pituitary Hypofunction

    dysgenesis ( Q99.1 ) hypopituitarism ( E23.0 ) Ahumada-del Castillo syndrome E23.0 Brissaud's infantilism or dwarfism E23.0 Cachexia R64 ICD-10-CM Diagnosis Code R64 Cachexia[icd10data.com] […] enemas or sodas, etidronate sodium) High Calcium levels Causes of Decreased Intracellular phosphorus shift Alkalosis or recovery from acidosis (COPD, Diabetic ketoacidosis[drkaslow.com] R62 Lack of expected normal physiological development in childhood and adults 2016 2017 2018 2019 Non-Billable/Non-Specific Code Type 1 Excludes delayed puberty ( E30.0 ) gonadal[icd10data.com]

    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.[ncbi.nlm.nih.gov] Generalized aminoaciduria and decreased tubular reabsorption of phosphate were also present.[ncbi.nlm.nih.gov] There may be increased or normal excretion of calcium, citrate, or phosphate in urine, while there may be decreased or normal excretion of NH 4 in the urine.[lecturio.com]

    Missing: Abnormal Corticomedullary Differentiation
  • Hypogonadism

    (primary hypogonadism) in females include the following: Turner syndrome Inactivating mutations XX and XY gonadal dysgenesis Premature menopause Radiation therapy Chemotherapy[emedicine.medscape.com] Myotonin (transfers phosphate to ATP) 10 11.[slideshare.net] Congenital causes include the following:[1][3][4] Chromosomal abnormalities (resulting in gonadal dysgenesis) - Turner's syndrome, Klinefelter's syndrome, Swyer's syndrome[en.wikipedia.org]

    Missing: Abnormal Corticomedullary Differentiation
  • Tumor Lysis Syndrome

    Another common feature of Turner syndrome is the failure of the ovaries to develop properly (gonadal dysgenesis).[rarediseases.org] […] binders, but HD or CVVHD is often used in refractory cases --caution of treating hypocalcemia before decreasing hyperphosphatemia as you can precipitate calcium phosphate[errolozdalga.com] 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]

  • Renal Transplant Rejection

    Renal parenchyma The superficial location of the renal transplant allows for normal corticomedullary differentiation of the renal parenchyma, with the medullary pyramids being[appliedradiology.com] Unfortunately, the sonographic appearance of many diffuse renal parenchymal abnormalities is nonspecific, including acute tubular necrosis (ATN), acute or chronic rejection[appliedradiology.com]

    Missing: female gonadal dysgenesis

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