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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2001-6-6
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pubmed:abstractText |
Kallmann's syndrome is characterized by anosmia and hypogonadotrophic hypogonadism. Radiographic studies of teenagers and older subjects with the X-linked form of the syndrome have shown that up to 40% have an absent kidney unilaterally. Although this has been attributed to renal "agenesis", a condition in which the kidney fails to form, little is known about the appearance of the developing urinary tract either pre- or post-natally in individuals with Kallmann's syndrome.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0931-0509
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1170-5
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11390716-Child, Preschool,
pubmed-meshheading:11390716-Female,
pubmed-meshheading:11390716-Fetus,
pubmed-meshheading:11390716-Gestational Age,
pubmed-meshheading:11390716-Humans,
pubmed-meshheading:11390716-Infant,
pubmed-meshheading:11390716-Kallmann Syndrome,
pubmed-meshheading:11390716-Male,
pubmed-meshheading:11390716-Multicystic Dysplastic Kidney,
pubmed-meshheading:11390716-Nephrectomy,
pubmed-meshheading:11390716-Nuclear Family,
pubmed-meshheading:11390716-Pedigree,
pubmed-meshheading:11390716-Pregnancy,
pubmed-meshheading:11390716-Ultrasonography, Prenatal,
pubmed-meshheading:11390716-X Chromosome
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pubmed:year |
2001
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pubmed:articleTitle |
Multicystic dysplastic kidney and Kallmann's syndrome: a new association?
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pubmed:affiliation |
Department of Child Health, The Royal Victoria Infirmary, Newcastle-upon-Tyne NE1 4LP, UK.
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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