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1,572 Possible Causes for Cystic Kidney

  • Fabry Disease

    Frequency United States Fabry disease is one of the more common lysosomal storage disorders, affecting approximately 1 in 40,000-60,000 males. Mortality/Morbidity Prior to the availability of renal transplant, dialysis, and, more recently, enzyme replacement therapy (ERT), the average age at death in men with classic[…][emedicine.com]

  • Cystic Kidney

    SUMMARY: At present, there are no specific treatments available for patients with cystic kidney disease.[ncbi.nlm.nih.gov] Abstract Cystic kidney disease is an important cause of chronic renal failure.[ncbi.nlm.nih.gov] In this Review we discuss a clinical approach to the diagnosis of cystic kidney diseases in adults, for use by nephrologists.[ncbi.nlm.nih.gov]

  • Meckel-Gruber Syndrome

    MGS, consisting of an occipital encephalocele, bilateral cystic kidneys and postaxial polydactyly, is a rare autosomal recessive disorder, with a recurrence risk of 25%.[ncbi.nlm.nih.gov] Meckel-Gruber syndrome (MKS) is an autosomal recessive, lethal multisystemic disorder characterized by meningooccipital encephalocele, cystic kidney dysplasia, hepatobiliary[ncbi.nlm.nih.gov] kidney dysplasia, hepatobiliary ductal plate malformation, and postaxial polydactyly.[ncbi.nlm.nih.gov]

  • Tuberous Sclerosis

    The association between cystic kidney disease and the tuberous sclerosis complex (TSC) is well known, but its presentation as a unilateral mass with glomerulocystic pattern[ncbi.nlm.nih.gov] Kidneys: Angiomyolipomas, cystic lesions. Angiomyolipomas are constituted of blood vessels, adipose tissue and connective tissue.[symptoma.com] False positives/negatives Cystic lesions of tuberous sclerosis may mimic simple renal cysts, as well as the cysts of autosomal-dominant polycystic kidney disease.[emedicine.com]

  • Medullary Sponge Kidney

    We observed a 30-year-old woman in whom a large mass in the right lower quadrant and bilaterally enlarged cystic kidneys with markedly distorted collecting systems by excretory[ncbi.nlm.nih.gov] […] by cystic dilatation of the medullary collecting ducts, resulting in a spongy gross appearance of the kidney.[icd9data.com] Codes ICD10CM: Q61.5 – Medullary cystic kidney SNOMEDCT: 236443009 – Medullary sponge kidney Differential Diagnosis & Pitfalls Differential diagnosis of medullary cystic lesions[visualdx.com]

  • Conn Syndrome

    This document is available in Spanish Treatment The best treatment for primary hyperaldosteronism Primary hyperaldosteronism - a disease where too much aldosterone is being made depends on the cause of the disease. Patients with unilateral disease should have an adrenalectomy Adrenalectomy - an operation to[…][web.archive.org]

  • Solitary Renal Cyst

    Over the past two decades, endoscopic surgery for cystic kidney disease minimize surgical trauma so that they became comparable to puncture techniques, and surpass them in[kazan-medjournal.ru] If your child has been diagnosed with kidney cystic disease, you may need to be tested. Some of the cystic kidney diseases in children are passed down from a parent.[urologyhealth.org] NIH: National Institute of Diabetes and Digestive and Kidney Diseases Acquired Cystic Kidney Disease - NIH (National Institute of Diabetes and Digestive and Kidney Diseases[icdlist.com]

  • Polycystic Kidney Disease

    Summary At present, there are no specific treatments available for patients with cystic kidney disease.[doi.org] These proteins, and many others associated with cystic kidney disease, localize to primary cilia, which may act as flow sensors in the kidney; cystic kidney diseases have[ncbi.nlm.nih.gov] […] disorders associated with kidney cysts, for example, tuberous sclerosis complex; and nongenetic forms of renal cystic disease, for example, simple kidney cysts.[ncbi.nlm.nih.gov]

  • Bilateral Multicystic Dysplastic Kidney

    Q61.8 Other cystic kidney diseases Q61.9 Cystic kidney disease, unspecified Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter Q62.0[icd10data.com] NIH: National Institute of Diabetes and Digestive and Kidney Diseases Acquired Cystic Kidney Disease - NIH (National Institute of Diabetes and Digestive and Kidney Diseases[icdlist.com] Cystic renal dysplasia, defined by microscopic features, is an anomaly of differentiation of the fetal kidney.[medhelp.org]

  • Medullary Cystic Kidney Disease

    CYSTIC KIDNEY DISEASE 2; MCKD2 Medullary Cystic Kidney Disease type 2 MCKD2 Medullary Cystic Kidney Disease 2, Autosomal Dominant MEDULLARY CYSTIC KIDNEY DISEASE 2 Medullary[wikidata.org] The diagnosis of medullary cystic kidney disease can be done via a physical exam.[en.wikipedia.org] Medullary cystic kidney disease is characterized by multiple renal cysts at the corticomedullary boundary area, by autosomal dominant inheritance, and by onset of chronic[ncbi.nlm.nih.gov]

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