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Sickle cell anemia

Sickle cell anemias are chronic hemolytic diseases that may induce three types of acute accidents: severe anemia, severe bacterial infections, and ischemic vasoocclusive accidents (VOA) caused by sickle-shaped red blood cells obstructing small blood vessels and capillaries. Many diverse complications can occur.

Glomerulonephritis

Inflammation of the renal glomeruli.

Total: 14

(per page)

PMID (PMCID)
29386039 (5793438)	FEMALE	Child
	Posterior reversible encephalopathy syndrome secondary to asymptomatic poststreptococcal glomerulonephritis in a child with sickle cell anemia: a case report.
	Hanafy E, Alshareef D, Osman S, Al Jabri A, Nazim F, Mahmoud G. J Med Case Rep. 2018;12(1):24.
	We report what is to our knowledge the first reported case of a 9-year-old Saudi girl with sickle cell anemia who developed posterior reversible encephalopathy syndrome secondary to asymptomatic poststreptococcal glomerulonephritis.
29386039 (5793438)	FEMALE	Child
	Posterior reversible encephalopathy syndrome secondary to asymptomatic poststreptococcal glomerulonephritis in a child with sickle cell anemia: a case report.
	Hanafy E, Alshareef D, Osman S, Al Jabri A, Nazim F, Mahmoud G. J Med Case Rep. 2018;12(1):24.
	Posterior reversible encephalopathy syndrome can be the presenting feature of postinfectious glomerulonephritis, which has been reported in approximately 5% of hospitalized children, and it has been reported in very few cases of adult patients with sickle cell anemia.
29386039 (5793438)	FEMALE	Child
	Posterior reversible encephalopathy syndrome secondary to asymptomatic poststreptococcal glomerulonephritis in a child with sickle cell anemia: a case report.
	Hanafy E, Alshareef D, Osman S, Al Jabri A, Nazim F, Mahmoud G. J Med Case Rep. 2018;12(1):24.
	Posterior reversible encephalopathy syndrome secondary to asymptomatic poststreptococcal glomerulonephritis in a child with sickle cell anemia: a case report.
25035790	OTHER
	A novel case report of sickle cell disease-associated immunoglobulin A nephropathy: the diagnostic value of erythrocyte dysmorphism evaluation.
	Silva GE, Teixeira AC, Vergna JG, Salgado-Filho N, Crivellentti LZ, Costa RS, Dantas M. Int J Clin Exp Med. 2014;7(6):1619-22.
	Despite the fact that immunoglobulin A nephropathy is the most commonly diagnosed glomerulonephritis worldwide, an association between this entity and sickle cell disease has not yet been reported, probably because all cases of hematuria in patients with sickle cell disease have been regarded as secondary to sickle cell disease.
25035790	OTHER
	A novel case report of sickle cell disease-associated immunoglobulin A nephropathy: the diagnostic value of erythrocyte dysmorphism evaluation.
	Silva GE, Teixeira AC, Vergna JG, Salgado-Filho N, Crivellentti LZ, Costa RS, Dantas M. Int J Clin Exp Med. 2014;7(6):1619-22.
	Despite the fact that immunoglobulin A nephropathy is the most commonly diagnosed glomerulonephritis worldwide, an association between this entity and sickle cell disease has not yet been reported, probably because all cases of hematuria in patients with sickle cell disease have been regarded as secondary to sickle cell disease.
25035790	OTHER
	A novel case report of sickle cell disease-associated immunoglobulin A nephropathy: the diagnostic value of erythrocyte dysmorphism evaluation.
	Silva GE, Teixeira AC, Vergna JG, Salgado-Filho N, Crivellentti LZ, Costa RS, Dantas M. Int J Clin Exp Med. 2014;7(6):1619-22.
	Despite the fact that immunoglobulin A nephropathy is the most commonly diagnosed glomerulonephritis worldwide, an association between this entity and sickle cell disease has not yet been reported, probably because all cases of hematuria in patients with sickle cell disease have been regarded as secondary to sickle cell disease.
18574127	MALE	Adult
	Focal Salmonella enteritidis infection in a patient with HIV infection and other multiple causes of immunodeficiency.
	Peppa D, Sutton JK, Bin-Reza F, Morris-Jones SD, Miller RF. Int J STD AIDS. 2008;19(7):491-2.
	An HIV-infected man receiving antiretroviral therapy-who also had lupus-like vasculitis and membranous glomerulonephritis (treated with prednisolone and azathioprine), beta-thalassaemia minor trait and post-radiotherapy functional asplenia (mimicking sickle cell disease-induced hyposplenism)-developed focal soft issue and bone infection caused by Salmonella enteritidis at the site of previous mycobacterial infection.
17973321	MALE	Child
	Sickle cell disease complicated by post-streptococcal glomerulonephritis, cerebral hemorrhage and reversible posterior leucoencephalopathy syndrome.
	Pashankar FD, Ment LR, Pearson HA. Pediatr Blood Cancer. 2008;50(4):864-6.
	Sickle cell disease complicated by post-streptococcal glomerulonephritis, cerebral hemorrhage and reversible posterior leucoencephalopathy syndrome.
9787325	FEMALE	Child
	Focal segmental glomerulosclerosis in children with acute lymphocytic leukemia: case reports and review of literature.
	Sathiapalan RK, Velez MC, McWhorter ME, Irwin K, Correa H, Baliga R, Warrier RP. J Pediatr Hematol Oncol. 1998;20(5):482-5.
	In both patients, no known etiologic factors, such as systemic lupus erythematosus, poststreptococcal glomerulonephritis, sickle cell anemia, or acquired immunodeficiency syndrome, were evident.
7637482	MIXED_SAMPLE	Child
	Glomerulonephritis after human parvovirus infection in homozygous sickle-cell disease.
	Wierenga KJ, Pattison JR, Brink N, Griffiths M, Miller M, Shah DJ, Williams W, Serjeant BE, Serjeant GR. Lancet. 1995;346(8973):475-6.
	Glomerulonephritis after human parvovirus infection in homozygous sickle-cell disease.
3252967	MALE	Child
	Acute poststreptococcal glomerulonephritis and sickle cell disease.
	Assar R, Pitel PA, Lammert NL, Tolaymat A. Child Nephrol Urol. 1988;9(3):176-9.
	Acute poststreptococcal glomerulonephritis and sickle cell disease.
3252967	MALE	Child
	Acute poststreptococcal glomerulonephritis and sickle cell disease.
	Assar R, Pitel PA, Lammert NL, Tolaymat A. Child Nephrol Urol. 1988;9(3):176-9.
	This presentation makes it difficult to differentiate acute glomerulonephritis from nephrotic syndrome associated with sickle cell disease.
3592455	FEMALE	Adult
	[Recurrent macroscopic hematuria and heterozygote drepanocytosis].
	Nedelec G, Didelot F, Giudicelli CP, Perrot S, Debord T, Brouard R, Rougier Y. Ann Med Interne (Paris). 1987;138(1):52-5.
	A proliferative mesangial glomerulonephritis with IgG, IgA, IgM and complement deposits, which has a controversial relationship with sickle cell disease, may be discovered by renal biopsy.
793378	MIXED_SAMPLE	Child
	Sickle-cell disease and poststreptococcal acute glomerulonephritis.
	Roy S, Murphy WM, Pitcock JA, Rimer RL. Am J Clin Pathol. 1976;66(6):986-90.
	Since proliferative glomerulonephritis of either poststreptococcal or non-poststreptococcal etiology may be seen in patients who have sickle-cell disease, immunofluorescence and/or electron microscopic examination is essential for accurate diagnosis.