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Oligomeganephronia
Congenital renal hypoplasia characterized by small kidneys; reduced nephron number; tubular and glomerular hypertrophy.(NICHD)
National Institutes of Health
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5 relations
Broader (1)
Congenital hypoplasia of kidney
Kidney
Kidney Diseases
Renal cysts and diabetes syndrome
Urinary system
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
A Novel Mutation of the HNF1B Gene Associated With Hypoplastic Glomerulocystic Kidney Disease and Neonatal Renal Failure
M. I. Alvelos
,
Magda Rodrigues
,
+4 authors
M. Lemos
Medicine
2015
Corpus ID: 16816375
AbstractHepatocyte nuclear factor 1 beta (HNF1B) plays an important role in embryonic development, namely in the kidney, pancreas…
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2013
2013
Congenital Oligomeganephronia: Computed Tomography Appearance
K. Hopkins
,
J. Mowry
,
D. Houghton
Clinics and Practice
2013
Corpus ID: 18245469
We report a case of congenital oligomeganephronia unexpectedly imaged with computed tomography (CT). Oligomeganephronia is a form…
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Review
2002
Review
2002
Oligonephropathy: from a rare childhood disorder to a possible health problem in the adult.
A. Drukker
The Israel Medical Association journal : IMAJ
2002
Corpus ID: 24641036
Recent data have shed significant new light on the structural and functional development of the kidneys, as well as on a rare…
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1997
1997
Ring chromosome 4 mosaicism coincidence of oligomeganephronia and signs of Seckel syndrome.
Carol E Anderson
,
Robert Wallerstein
,
+4 authors
Laird G. Jackson
American journal of medical genetics
1997
Corpus ID: 36940608
We present a patient with features suggestive of Seckel syndrome who was found to be mosaic for ring 4 chromosome. Seckel…
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1993
1993
Oligomeganephronia associated with 4p deletion type chromosomal anomaly.
Sung-Hye Park
,
Je G. Chi
Pediatric Pathology
1993
Corpus ID: 20518081
Oligomeganephronia is a rare congenital renal hypoplasia that is characterized histologically by a reduction in the number of…
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1990
1990
Focal glomerular sclerotic lesions in a patient with unilateral oligomeganephronia and agenesis of the contralateral kidney: a case report.
S. Nomura
,
G. Osawa
Clinical Nephrology
1990
Corpus ID: 22061076
An open renal biopsy specimen from a twelve-year-old boy with a congenital solitary kidney was studied with light, electron, and…
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1989
1989
Acrorenal syndrome in an adult--presentation with proteinuria, hypertension, and glomerular lesions.
M. Zeier
,
G. Tariverdian
,
R. Waldherr
,
K. Andrassy
,
E. Ritz
American Journal of Kidney Diseases
1989
Corpus ID: 10275004
1985
1985
FAMILIAL OCCURRENCE OF OLIGOMEGANEPHRONIA
Y. Kusuyama
,
R. Tsukino
,
+4 authors
Koji Saito
Acta pathologica japonica
1985
Corpus ID: 38738068
Oligomeganephronia (OMN) is a rare, renal hypoplasia, consisting of reduced number of hypertrophied nephrons. This disorder has…
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1973
1973
Bilateral renal hypoplasia with oligomeganephronia: quantitative and electron microsopic study.
T. Morita
,
J. Wenzl
,
J. McCoy
,
J. Porch
,
P. Kimmelstiel
American Journal of Clinical Pathology
1973
Corpus ID: 19170289
The case of a 12-year-old boy with oligomeganephronic renal hypoplasia is reported. On light microscopy the histologic findings…
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1970
1970
Bilateral renal hypoplasia with oligomeganephronia. Oligomeganephronic renal hypoplasia.
J. E. Carter
,
D. Lirenman
A M A Journal of Diseases of Children
1970
Corpus ID: 38606640
The syndrome of congenital bilateral renal hypoplasia with hypertrophy of nephrons has been well documented in the French…
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