- A Case of Anterior Lenticonus in Alport's Syndrome
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Lee HL, Rhee MR, Shim YB, Kim BC
- KMID: 1949303
- J Korean Ophthalmol Soc.
- 1989 Apr;30(2):305-309.
Alport's syndrome, first described by Alport in 1927, is a clinical entity which consists of lens abnormalities, hereditary hemorrhagic nephritis and nerve deafness. Anterior lenticonus is a rare structual anomaly... -
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- A Case of Epstein's Syndrome
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Choi SY, Chae HC, Cho HY, Kim HB, Oh JS
- KMID: 2208423
- J Korean Pediatr Soc.
- 1994 Nov;37(11):1610-1614.
Epstein's syndrome is a rare disease whish is characterized by the association of thrombocytopenia, macrothrombocytopathia, nephritis and deafness. We experienced a case of Epstein's syndrome in a 12 years old... -
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- A Case of Alport's Syndrome
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Lee JB, Lee JK, Kim PK, Jeong HJ, Choi IJ
- KMID: 1677120
- J Korean Pediatr Soc.
- 1987 Sep;30(9):1040-1048.
No abstract available. -
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- Familial diffuse gastroesophageal leiomyomatosis: A presentation in a mother and her son with Alport syndrome
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Moon SM, Chang YW, Jang JY, Kim YW, Kim HJ, Kim BH, Chang R
- KMID: 2259119
- Korean J Med.
- 2010 Aug;79(2):171-176.
Diffuse gastroesophageal leiomyomatosis is a rare, benign neoplastic condition characterized by thickening of the esophageal wall as a result ofaberrant smooth muscle proliferation. Gastroesophageal leiomyomatosis may occur in isolation or... -
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- Alport's syndrome: A case report
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Kim JH, Kim HC, Kim SJ, Park KK
- KMID: 1684599
- Korean J Otolaryngol-Head Neck Surg.
- 1993 Feb;36(1):156-163.
No abstract available. -
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- Anterior Lens Capsule Abnormalities in Alport Syndrome
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Choi JH, Na KS, Bae SH, Roh GH
- KMID: 1099092
- Korean J Ophthalmol.
- 2005 Mar;19(1):84-89.
- doi: 10.3341/kjo.2005.19.1.84
Alport syndrome is a hereditary, progressive disease characterized by progressive nephritis, sensorineural deafness, and ocular abnormalities, including anterior lenticonus. The ultrastructure of the lens capsule abnormalities in Alport syndrome is... -
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- Clinical studies of 12 cases on alport's syndrome
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Lee JS, Park IJ, Pai KS, Lee JS, Kim PK, Choi YJ, Jeong HJ, Choi IJ
- KMID: 1694559
- Korean J Nephrol.
- 1993 Sep;12(3):440-451.
No abstract available. -
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- Alport Syndrome Associated with Poststreptococcal Glomerulonephritis in Brothers
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Shin HK, Kim JH, Yoo KH, Hong YS, Lee JW, Kim SK, Won NH, Cheong HI
- KMID: 2197720
- J Korean Soc Pediatr Nephrol.
- 2003 Apr;7(1):67-72.
Alport syndrome is the most common type of hereditary nephritis, and acute poststreptococcal glomerulonephritis(APSGN) is a common disease in children. We experienced the clinical and pathologic findings of Alport syndrome... -
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- Genetic diagnosis of Alport syndrome
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Cheong HI
- KMID: 2451965
- Korean J Pediatr.
- 2019 May;62(5):164-165.
- doi: 10.3345/kjp.2018.07339
No abstract available. -
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- Two cases of Alport syndrome developed in sister
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Park VH, Park J, Cho SY, Cha SH, Cho BS, Ahn CI, Hong SD, Yang MH
- KMID: 1690983
- J Korean Pediatr Soc.
- 1992 Sep;35(9):1314-1319.
No abstract available. -
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- A Case of Alport's Syndrome in an Adult
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Kim HS, Rho YH, An M, Jun JG, Cha YH, Ahn HS, Kim YJ, Park BY, Kim YK, Oh YH
- KMID: 1990088
- Korean J Nephrol.
- 1999 Mar;18(2):329-333.
Alport's syndrome is a hereditary disorder whose incidence is 1 in 10,000 in general population, and, majority are developed in childhood, so it is rare to develop in adults. This syndrome consists... -
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- Analysis of 1559 Kidney Biopsies: A Single Center Study
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Choi YS, Kim SK, Kim SD, Cho BS
- KMID: 2098848
- J Korean Soc Pediatr Nephrol.
- 2006 Oct;10(2):174-181.
PURPOSE: To analyse the results of the renal biopsies and the clinical diagnoses of patients who had undergone percutaneous kidney biopsies in the department of pediatrics at Kyunghee University Hospital... -
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- A Case of Alport's Syndrome in an Adult
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Park SI, Kim W, Park SK, Kang SK, Kang MJ
- KMID: 2079129
- Korean J Nephrol.
- 2000 Jul;19(4):760-764.
Alport's syndrome is a progressive hereditary kidney disease. The disease is primarily X chromosome- linked but autosomal forms have also been reported. The authors experienced a case of Alport's syndrome... -
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- Clinicopathological Study on Adult Nephrotic Syndrome
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Oh KH, Ahn CR, Yang JS, Hwang DY, Han JS, Kim SG, Lee JS, Lee HS
- KMID: 2254839
- Korean J Nephrol.
- 1997 Jun;16(2):254-265.
We investigated the clinical features of nephrotic syndrome in Korea according to sex, age and pathologic diagnosis under the classification system supported by WHO. Adult nephrotic patients who underwent renal... -
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- Angiotensin Converting Enzyme Gene Polymorphism in Alport Syndrome
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Kim JH, Lee JS, Kim PK
- KMID: 2197649
- J Korean Soc Pediatr Nephrol.
- 2004 Apr;8(1):18-25.
PURPOSE: Alport syndrome is clinically characterized by hereditary progressive nephritis causing ESRD with irregular thickening of the GBM and sensory neural hearing loss. The mutations of type IV collagen gene(COL4A5)... -
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- De novo mutations in COL4A5 identified by whole exome sequencing in 2 girls with Alport syndrome in Korea
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Han KH, Park JE, Ki CS
- KMID: 2451970
- Korean J Pediatr.
- 2019 May;62(5):193-197.
- doi: 10.3345/kjp.2018.06772
Alport syndrome (ATS) is an inherited glomerular disease caused by mutations in one of the type IV collagen novel chains (α3, α4, and α5). ATS is characterized by persistent microscopic... -
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- Diffuse Esophageal Leiomyomatosis in a Child with Alport Syndrome: Case Report
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Ko HS, Goo HW, Yoon CH
- KMID: 1593969
- J Korean Radiol Soc.
- 2004 May;50(5):375-378.
- doi: 10.3348/jkrs.2004.50.5.375
Diffuse esophageal leiomyomatosis is an exceedingly rare, benign, neoplastic condition occurring predominantly in children and young adults. This condition may occur as an isolated finding, or it may be associated... -
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- The Effect of Recombinant Human Growth Hormone on Growth in Children with Nephropathy Receiving Long-term Steroid Therapy
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Kim SJ, Kim SK, Kim SD, Cho BS
- KMID: 2098845
- J Korean Soc Pediatr Nephrol.
- 2006 Oct;10(2):142-151.
PURPOSE: Growth retardation is one of the serious problems in children with nephropathy requiring long-term steroid therapy. We observed the efficacy and safety of recombinant human growth hormone(rhGH) on the... -
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- Endolymphatic Hydrops: Pathophysiology and Etiology
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Nam SI
- KMID: 2074178
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2011 Aug;54(8):509-518.
- doi: 10.3342/kjorl-hns.2011.54.8.509
Endolymphatic hydrops (EH) represents a histopathologic finding in which the structures bounding the endolymphatic space are distended by an enlargement of endolymphatic volume. EH primarily involves the cochlear duct and... -
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- Two Cases of Thin Basement Membrane Nephropathy presented with Minimal Change Nephrotic Syndrome
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Seo YM, Chung JG, Yu ES, Jeong JY, Park YS
- KMID: 2335501
- J Korean Pediatr Soc.
- 2000 Jul;43(7):978-982.
Thin basement membrane nephropathy(TBMN) is defined histologically as follows: 1) By light rnicroscopy only minor abnormalities are detected in the glomeruli at most minor mesangial widening. 2) By electron microscopy, diffuse thinning... -
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