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pubmed-article:11390716pubmed:dateCreated2001-6-6lld:pubmed
pubmed-article:11390716pubmed:abstractTextKallmann'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.lld:pubmed
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pubmed-article:11390716pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:11390716pubmed:year2001lld:pubmed
pubmed-article:11390716pubmed:articleTitleMulticystic dysplastic kidney and Kallmann's syndrome: a new association?lld:pubmed
pubmed-article:11390716pubmed:affiliationDepartment of Child Health, The Royal Victoria Infirmary, Newcastle-upon-Tyne NE1 4LP, UK.lld:pubmed
pubmed-article:11390716pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11390716pubmed:publicationTypeCase Reportslld:pubmed
pubmed-article:11390716pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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