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Acrorenal Syndrome

 
National Institutes of Health

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2017
2017
У статті автори аналізують дані літератури, а також результати власного багаторічного досвіду діагностики генетично детермінованих захворювань нирок, що супроводжувалися розвитком хронічної ниркової недостатності. Викладено основні причини захворювань, принципи їх діагностики та лікування. Наведено клінічне спостереження за пацієнтом з акроренальним синдромом, ускладненим розвитком хронічної ниркової недостатності. 
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2006
2006
This case reports a delivery of a child with limb and renal malformations following intracytoplasmic sperm injection. A 29-year… Expand
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2004
2004
Dieker and Opitz in 1969 described the simultaneous occurrence of limb deficiencies (LDs) and renal anomalies (RAs) in three… Expand
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2004
2004
The case of a 2-year-old boy with associated anomalies of the limbs and the urinary system is reported. Similar to cases reported… Expand
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1999
1999
  • M. Zeier, E. Ritz
  • Nephrology, dialysis, transplantation : official…
  • 1999
  • Corpus ID: 28264006
 
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1996
1996
Abstract.The clinical, biochemical, radiological, and histological data of a 5-year-old boy with severe limb deformities and… Expand
  • figure 1
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1996
1996
The clinical biochemical, radiological, and histological data of a 5-year-old boy with severe limb deformities and renal failure… Expand
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Review
1992
Review
1992
A 23-year-old female patient with the acrorenal syndrome is described. In addition to acral and renal malformations, she had… Expand
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1989
1989
Acrorenal syndrome is characterized by central longitudinal axis defects of the limbs, ie, split hand and/or foot. Associated… Expand
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1988
1988
This paper describes an 18‐year‐old patient with Rokitansky‐Küster‐Hauser (R‐K‐H) syndrome. In this case, apart from the usual… Expand
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