rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
1
|
pubmed:dateCreated |
1984-6-11
|
pubmed:abstractText |
The case of a 2-year-old boy with associated anomalies of the limbs and the urinary system is reported. Similar to cases reported earlier he presented a split hand and foot syndrome, but differed from previously reported cases by the presence of bilateral renal hypoplasia leading to end stage renal failure. Renal histology disclosed oligomeganephronia.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0340-6199
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
142
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
40-3
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:6714259-Abnormalities, Multiple,
pubmed-meshheading:6714259-Adult,
pubmed-meshheading:6714259-Foot Deformities, Congenital,
pubmed-meshheading:6714259-Growth Disorders,
pubmed-meshheading:6714259-Hand Deformities, Congenital,
pubmed-meshheading:6714259-Humans,
pubmed-meshheading:6714259-Infant, Newborn,
pubmed-meshheading:6714259-Kidney,
pubmed-meshheading:6714259-Kidney Failure, Chronic,
pubmed-meshheading:6714259-Male,
pubmed-meshheading:6714259-Nephrons,
pubmed-meshheading:6714259-Syndrome
|
pubmed:year |
1984
|
pubmed:articleTitle |
A new variant of the acrorenal syndrome associated with bilateral oligomeganephronic hypoplasia.
|
pubmed:publicationType |
Journal Article,
Case Reports
|