Growth and pubertal development in five boys with Noonan's syndrome.
Identifieur interne : 004596 ( Pmc/Checkpoint ); précédent : 004595; suivant : 004597Growth and pubertal development in five boys with Noonan's syndrome.
Auteurs : G. Theintz ; M. O. SavageSource :
- Archives of Disease in Childhood [ 0003-9888 ] ; 1982.
Abstract
Five boys, each with at least 4 features characteristic of Noonan's syndrome, were studied throughout childhood. In each the height was on or below the 3rd centile. Height velocity was essentially normal during the prepubertal period whereas bone age and pubertal development were delayed. Four boys had cryptorchidism and in 2 no testicular enlargement or spontaneous puberty occurred, necessitating testosterone replacement. Plasma concentrations of luteinising hormone and follicle-stimulating hormone before and after stimulation with luteinising hormone-releasing hormone were increased in 4 of the boys. These findings are consistent with primary gonadal failure associated with impaired spermatogenesis.
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PubMed: 6121534
PubMed Central: 2863270
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<front><journal-meta><journal-id journal-id-type="nlm-ta">Arch Dis Child</journal-id><journal-id journal-id-type="pmc">archdisch</journal-id><journal-title>Archives of Disease in Childhood</journal-title><issn pub-type="ppub">0003-9888</issn><issn pub-type="epub">1468-2044</issn><publisher><publisher-name>BMJ Group</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">6121534</article-id><article-id pub-id-type="pmc">2863270</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title>Growth and pubertal development in five boys with Noonan's syndrome.</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Theintz</surname><given-names>G.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Savage</surname><given-names>M. O.</given-names></name></contrib></contrib-group><pub-date pub-type="ppub"><month>1</month><year>1982</year></pub-date><volume>57</volume><issue>1</issue><fpage>13</fpage><lpage>17</lpage><abstract><p>Five boys, each with at least 4 features characteristic of Noonan's syndrome, were studied throughout childhood. In each the height was on or below the 3rd centile. Height velocity was essentially normal during the prepubertal period whereas bone age and pubertal development were delayed. Four boys had cryptorchidism and in 2 no testicular enlargement or spontaneous puberty occurred, necessitating testosterone replacement. Plasma concentrations of luteinising hormone and follicle-stimulating hormone before and after stimulation with luteinising hormone-releasing hormone were increased in 4 of the boys. These findings are consistent with primary gonadal failure associated with impaired spermatogenesis.</p></abstract></article-meta></front></pmc><affiliations><list></list><tree><noCountry><name sortKey="Savage, M O" sort="Savage, M O" uniqKey="Savage M" first="M. O." last="Savage">M. O. Savage</name><name sortKey="Theintz, G" sort="Theintz, G" uniqKey="Theintz G" first="G." last="Theintz">G. Theintz</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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