Matches in SemOpenAlex for { <https://semopenalex.org/work/W2071488315> ?p ?o ?g. }
Showing items 1 to 69 of
69
with 100 items per page.
- W2071488315 endingPage "130s" @default.
- W2071488315 startingPage "125s" @default.
- W2071488315 abstract "La puberté correspond à un ensemble de phénomènes complexes de maturation neuroendocrinienne qui amènent un individu à un stade de développement permettant la reproduction. Le retard pubertaire (RP) est défini chez le garçon par l'absence de développement testiculaire au-delà de l'âge de 14 ans (< 4 ml), et chez la fille par l'absence de développement mammaire au-delà de 13 ans. La prévalence du RP est estimée à environ 3 %. Dans la majorité des cas, il s'agit d'un RP fonctionnel, notamment d'un retard simple (le plus souvent familial), de bon pronostic. Mais le RP peut être dû à un hypogonadisme hypogonadotrope, d'origine haute, ou à un hypogonadisme hypergonadotrope, d'origine périphérique. Le syndrome de Turner doit être évoqué devant tout retard pubertaire chez la fille. Grâce à la biologie moléculaire, de nouvelles avancées ont permis d'expliquer certaines formes d'hypogonadisme hypogonadotrope et devraient aboutir à une meilleure compréhension des mécanismes neuroendocriniens de l'initiation de la puberté. Le retard pubertaire simple doit rester un diagnostic d'élimination. Outre la prise en charge de la cause si elle est possible, le traitement repose sur l'administration des stéroïdes sexuels.Puberty is the phenomenon that conducts once to reproductive maturation. Delayed puberty (DP) is defined by the absence of testicular development in boys beyond 14 years old (or a testicular volume lower than 4 ml) and by the absence of breast development in girls beyond 13 years old. DP occurs in approximatively 3% of cases. Most cases are functional DP, with a large amount of constitutional delay of puberty. Others etiologies are hypogonadotrophic hypogonadism like Kallmann syndrome, or hypergonadotrophic hypogonadism. Turner syndrome is a diagnostic one should not forget by its frequency. Treatment is hormonal replacement therapy and of the etiology. During the last decade, many genes have been identified and elucidated the etiological diagnosis of some hypogonadotrophic hypogonadism syndrome. Further studies are required in collaboration with molecular biologists to better understand the mechanism of hypothalamic pituitary gonadal axis abnormalities and of the neuroendocrine physiology of the onset of puberty." @default.
- W2071488315 created "2016-06-24" @default.
- W2071488315 creator A5084364519 @default.
- W2071488315 date "1997-01-01" @default.
- W2071488315 modified "2023-09-26" @default.
- W2071488315 title "Lémpreinte génomique parentale et ses implications dans la croissance" @default.
- W2071488315 cites W1502331465 @default.
- W2071488315 cites W1515636671 @default.
- W2071488315 cites W1552460297 @default.
- W2071488315 cites W1565038541 @default.
- W2071488315 cites W1588409425 @default.
- W2071488315 cites W1812913066 @default.
- W2071488315 cites W1972779402 @default.
- W2071488315 cites W2000488799 @default.
- W2071488315 cites W2007214149 @default.
- W2071488315 cites W2017278367 @default.
- W2071488315 cites W2043882061 @default.
- W2071488315 cites W2044894134 @default.
- W2071488315 cites W2046241907 @default.
- W2071488315 cites W2050384177 @default.
- W2071488315 cites W2059267677 @default.
- W2071488315 cites W2069169829 @default.
- W2071488315 cites W2071701929 @default.
- W2071488315 cites W2075942120 @default.
- W2071488315 cites W2078594244 @default.
- W2071488315 cites W2083813589 @default.
- W2071488315 cites W2088118447 @default.
- W2071488315 cites W2102277969 @default.
- W2071488315 cites W2102749853 @default.
- W2071488315 cites W2124500141 @default.
- W2071488315 cites W2139454112 @default.
- W2071488315 cites W2144750978 @default.
- W2071488315 cites W2163035954 @default.
- W2071488315 cites W2163679869 @default.
- W2071488315 cites W2404239634 @default.
- W2071488315 cites W2405908223 @default.
- W2071488315 doi "https://doi.org/10.1016/s0929-693x(97)86478-0" @default.
- W2071488315 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9246319" @default.
- W2071488315 hasPublicationYear "1997" @default.
- W2071488315 type Work @default.
- W2071488315 sameAs 2071488315 @default.
- W2071488315 citedByCount "0" @default.
- W2071488315 crossrefType "journal-article" @default.
- W2071488315 hasAuthorship W2071488315A5084364519 @default.
- W2071488315 hasConcept C29456083 @default.
- W2071488315 hasConcept C71924100 @default.
- W2071488315 hasConceptScore W2071488315C29456083 @default.
- W2071488315 hasConceptScore W2071488315C71924100 @default.
- W2071488315 hasLocation W20714883151 @default.
- W2071488315 hasLocation W20714883152 @default.
- W2071488315 hasOpenAccess W2071488315 @default.
- W2071488315 hasPrimaryLocation W20714883151 @default.
- W2071488315 hasRelatedWork W1995515455 @default.
- W2071488315 hasRelatedWork W1999344589 @default.
- W2071488315 hasRelatedWork W2039318446 @default.
- W2071488315 hasRelatedWork W2080531066 @default.
- W2071488315 hasRelatedWork W2748952813 @default.
- W2071488315 hasRelatedWork W2789448498 @default.
- W2071488315 hasRelatedWork W2899084033 @default.
- W2071488315 hasRelatedWork W3031052312 @default.
- W2071488315 hasRelatedWork W3032375762 @default.
- W2071488315 hasRelatedWork W3108674512 @default.
- W2071488315 hasVolume "4" @default.
- W2071488315 isParatext "false" @default.
- W2071488315 isRetracted "false" @default.
- W2071488315 magId "2071488315" @default.
- W2071488315 workType "article" @default.