Klinefelter Syndrome

Kukhona izifo ukuthi kunzima ukuthola bese elapha isikhathi. Omunye wabo Klinefelter syndrome. Kuyinto kofuzo kubangelwa isethi engalungile wama-chromosomes ocansini. Ngokuvamile, i-chromosome womuntu 46, emibili yayo ukucacisa XY phansi, kuyilapho iziguli extra X-chromosome futhi isakhi sofuzo simiswe ngalendlela lelandzelako: 47 XXY, nakuba zingase zibe khona ezinye ezahlukeneyo, isib, chromosome angu-48, lapho XXXY noma XXYY. Mosaicism futhi kwenzeka, kusho ukuthi abanye amaseli isethi evamile wama-chromosomes 46 XY kanti enye ingxenye yaba - washintsha ukuze 47 XXY.

X-chromosome kungowesifazane futhi luthathwe unina, futhi Y - amadoda (esivela kubaba). chromosome umama okweqile ubangela izinguquko emzimbeni womfana, ikakhulukazi okuhlobene umsebenzi zokuzala. Izibalo zibonisa ukuthi kwezinso zofuzo kuvamile ezinganeni azalelwa omama eminyakeni engu-40, kuyilapho ubudala ubaba ku nokudlondlobala awukho umphumela.

Klinefelter Syndrome, izimpawu

Sivame ukucabanga ukuthi izifo zofuzo umuntu ziyabonakala lapho ezalwa ezifana -Down syndrome. Kodwa kungenjongo Klinefelter Syndrome ukuba usakhula ukuthola kunzima usola. Duzane 14-15 iminyaka ziqala ukubonisa izimpawu zokuqala - ukukhula okungaphezu kwe-avareji, nge nemilenze uhlasela ezinde zomzimba ngohlobo besifazane kwenzeka endaweni pubic, kanti kwezinye izindawo kukhona cishe awekho izinwele. Chest ukwanda kancane kancane, ubukhulu amasende ahlale amancane.

Ngokocansi indoda ovuthiwe abakwazi ukuphila ukuphila ubulili evamile, yena wayehlushwa isifo Erectile Dysfunction ne orgasm omnene. Ngenxa yalokhu, ekuthuthukiseni nokugula ngengqondo, umuntu eba 'idla yodwa, kodwa udokotela wenqaba ukuya, osho ukuthi konke ukuze.

I degree of akahlakaniphile incike isibalo ezingadingekile X-chromosome. Ngokuvamile kukhona okuncane ukubambezeleka kwengqondo, kodwa abadala ke kungenziwa ngokuphelele ukunganakwa. Nokho, iziguli enjalo zithambekele isithuthwane.

Ngokuvamile, zonke lezi zici ehlangana ezinye izifo letindzala, ezifana nesifo samaphaphu, sikashukela mellitus, ukukhumuzeka kwamathambo noma izinkinga zendlala yegilo.

Klinefelter syndrome, uphethwe

Ngemva syndrome esolwa izici zangaphandle, indoda noma ingane iqondiswa i endocrinology. Kuthiwa ama-hormone Ukuhlaziywa ebonisa ukuthi igazi kweziguli okuqukethwe okhushuliwe hormone follicle-kuqabula futhi testosterone futhi androsterone iyohlale encishisiwe.

Uma nje ukuchitha karyotyping - ukuzimisela inani lezakhi zofuzo - nokwenza ipasipoti zofuzo, asikho esinye ukuhlolwa lwadlulela. Lolu cwaningo ihlinzeka yi-100%.

Ngokuvamile izici ezifana ukukhuluphala, gynecomastia (webele ukukhulisa) kwamathambo e intsha esikhulakhulile kwesokunxele ngaphandle usizo lwezokwelapha. Nokho, ngisho zizathu zixwaywe isifo, njengoba konke okuhlobene yokuntuleka kwe-testosterone emzimbeni. Lokhu kwakubangelwa ukukhumuzeka kwamathambo ubhekwa ukuba isifo zesifazane, futhi isifo asebekhulile.

Klinefelter Syndrome, ukwelashwa

Okuwukuphela indlela yokwelashwa yalesi sifo - the testosterone-hormone okuthiwa i replacement therapy izidakamizwa. Ukwelashwa kuyinto efiselekayo baqale ngokushesha ngangokunokwenzeka, kodwa sitholakele nobunzima ukucacisa isifo cishe akunakwenzeka nokuthomba.

Kuthiwa ama-hormone ubuyisele indoda izici zakhe zobulili, ukwandisa isifiso sobulili, kodwa awayilaphi nenzalo. Lena into kuphela ukuthi uhlala ingashintshiwe: Amadoda Klinefelter Syndrome nanini abe nezingane, abakwazi ekhiqiza isidoda njalo.

Ukwelashwa Kwenziwa ukuphila futhi ukunika ezinhle omuhle, kubuyisele ukuzethemba indoda.

Kukholakala ukuthi ekuhlonzweni (eneminyaka engu-7) uvumela isikhathi aqale ukwelashwa futhi inikeza ithuba lokuthuthukisa nokusebenzisa emasendeni ngokugcwele, okusho ukuthi umuntu angaba nezingane.