Uyichonga njani kwaye uyinyanga njani i-Klinefelter Syndrome

Umxholo

• Iimpawu eziphambili
• Kutheni iKlinefelter's syndrome isenzeka
• Indlela yokuqinisekisa ukuxilongwa
• Unyango lwenziwa njani

I-Klinefelter's syndrome yinto enqabileyo yemfuza echaphazela kuphela amakhwenkwe kwaye ivele ngenxa yobukho be-X chromosome eyongezelelweyo kwisibini sesini. Le chromosomal anomaly, ebonakaliswa yi-XXY, ibangela utshintsho kuphuhliso lomzimba kunye nokuqonda, ukuvelisa iimpawu ezibonakalayo ezinje ngokukhulisa isifuba, ukungabikho kweenwele emzimbeni okanye ukulibaziseka kuphuhliso lobudoda, umzekelo.

Nangona kungekho lunyango kwesi sifo, kunokwenzeka ukuba uqale unyango lwe-testosterone endaweni yokufikisa, evumela amakhwenkwe amaninzi ukuba akhule ngokufanayo kubahlobo bawo.

Iimpawu eziphambili

Amanye amakhwenkwe ane-Klinefelter's syndrome angangabonakalisi naluphi na utshintsho, nangona kunjalo, abanye banokuba neempawu ezithile zomzimba ezinje:

• Amasende amancinci kakhulu;
• Kancinci amabele amakhulu;
• Iinqe ezinkulu;
• Zimbalwa iinwele zobuso;
• Ubungakanani bepenisi encinci;
• Ilizwi liphezulu kunesiqhelo;
• Ukungachumi.

Ezi mpawu kulula ukuba zichongwe ngexesha lokufikisa, njengoko kuxa ukukhula kwamakhwenkwe kulindeleke ukuba kwenzeke. Nangona kunjalo, zikho ezinye izinto ezinokuthi zichongwe ukusukela ebuntwaneni, ngakumbi ezinxulumene nokukhula kwengqondo, njengokufumana ubunzima ekuthetheni, ukulibaziseka ekurhubuluzeni, iingxaki ekugxileni okanye ekubonakaliseni ubunzima.

Kutheni iKlinefelter's syndrome isenzeka

I-Klinefelter's syndrome yenzeka ngenxa yotshintsho kwimfuza ebangela ukuba i-X chromosome eyongezelelweyo ibekho kwi-karyotype yenkwenkwe, ibe yi-XXY endaweni ye-XY.

Nangona sisifo semfuza, esi sifo sivela kuphela kubazali siye ebantwaneni kwaye, ke, akukho thuba likhulu lokuba nesi sifo, nokuba sele kukho ezinye iimeko kusapho.

Indlela yokuqinisekisa ukuxilongwa

Ngokubanzi, urhano lokuba inkwenkwe inokuba nesifo sikaKlinefelter sivela ngexesha lokufikisa xa amalungu esini engakhuli kakuhle. Ke, ukuze kuqinisekiswe ukuxilongwa, kuyacetyiswa ukuba ubonane nogqirha wabantwana ukuba enze uvavanyo lwekaryotype, apho kuvavanywa khona ii-chromosomes zesini, ukuqinisekisa ukuba akukho zibini ze-XXY na.

Ukongeza kolu vavanyo, kumadoda amadala, ugqirha unokuyalela ezinye iimvavanyo ezinje ngovavanyo lwehomoni okanye umgangatho wesidoda, ukunceda ukuqinisekisa isifo.

Unyango lwenziwa njani

Akukho lunyango lwe-Klinefelter's syndrome, kodwa ugqirha unokukucebisa ukuba ubuyisele i-testosterone ngenaliti kulusu okanye ngokufaka ii-patches, ezithi zikhuphe i-hormone ngokuthe ngcembe ngokuhamba kwexesha.

Kwiimeko ezininzi, olu nyango luneziphumo ezingcono xa luqala kwinqanaba lokufikisa, njengoko ilixesha apho amakhwenkwe ephuhlisa khona iimpawu zawo zesini, kodwa inokwenziwa nakwabantu abadala, ikakhulu ukunciphisa ezinye zeempawu ezinje ngobungakanani beebele okanye ukuphakama kwelizwi.

Kwiimeko apho kukho ukulibaziseka kwengqondo, kuyacetyiswa ukuba unyango lube neengcali ezifanelekileyo. Umzekelo, ukuba kukho ubunzima ekuthetheni, kuyacetyiswa ukuba udibane nengcali yezentetho, kodwa olu hlobo lokulandela lungaxoxwa kugqirha wabantwana.