Ungayibona Kanjani futhi Uyiphathe Klinefelter Syndrome

-Delile

• Izici eziyinhloko
• Kungani kwenzeka i-Klinefelter syndrome
• Ungakuqinisekisa kanjani ukuxilongwa
• Yelashwa kanjani

I-Klinefelter syndrome isifo esingajwayelekile sezakhi zofuzo esithinta kuphela abafana futhi sivele ngenxa yokuba khona kwe-X chromosome eyengeziwe kubhangqwana bezocansi. Lokhu kwe-chromosomal anomaly, okubonakala nge-XXY, kubangela ushintsho ekukhuleni ngokomzimba nangokwengqondo, okwenza izici ezibalulekile njengokukhuliswa kwamabele, ukungabikho kwezinwele emzimbeni noma ukubambezeleka ekukhuleni kwepenisi, ngokwesibonelo.

Yize lungekho ikhambi lalesi sifo, kungenzeka ukuqala ukwelashwa okufaka esikhundleni se-testosterone ngesikhathi sobusha, okuvumela abafana abaningi ukuthi bakhule ngokufana kakhulu nabangane babo.

Izici eziyinhloko

Abanye abafana abane-Klinefelter's syndrome kungenzeka bangakhombisi izinguquko, kepha abanye bangaba nezici ezithile zomzimba ezinjenge:

• Amasende amancane kakhulu;
• Amabele amancane kakhulu;
• Okhalweni ezinkulu;
• Zimbalwa izinwele zobuso;
• Usayizi wepipi omncane;
• Izwi eliphakeme kunokujwayelekile;
• Ukungabi nenzalo.

Lezi zici kulula ukuzibona ngesikhathi sobusha, njengoba kulindeleke ukuthi ukukhula kwabafana kwezocansi kulindeleke ukuthi kwenzeke. Kodwa-ke, kunezinye izici ezingabonakala kusukela ebuntwaneni, ikakhulukazi ezihlobene nokukhula kwengqondo, njengokuthola ubunzima ekukhulumeni, ukubambezeleka ekukhasheni, izinkinga ekugxileni noma ebunzimeni bokuveza imizwa.

Kungani kwenzeka i-Klinefelter syndrome

I-Klinefelter syndrome yenzeka ngenxa yokuguqulwa kwezakhi zofuzo okwenza i-X chromosome eyengeziwe ibe khona ku-karyotype yomfana, eyi-XXY esikhundleni se-XY.

Yize kuyinkinga yezofuzo, lesi sifo sivela kubazali kuphela ezinganeni futhi, ngakho-ke, alikho ithuba elikhulu lokuba nalesi sifo, noma ngabe kukhona amanye amacala emndenini.

Ungakuqinisekisa kanjani ukuxilongwa

Ngokuvamile, izinsolo zokuthi umfana angaba ne-Klinefelter's syndrome zivela ngesikhathi sobusha lapho izitho zocansi zingakhuli kahle. Ngakho-ke, ukuqinisekisa ukuxilongwa, kungakuhle uthintane nodokotela wezingane ukuze wenze ukuhlolwa kwe-karyotype, lapho kuhlolwa khona ama-chromosomes ocansi, ukuqinisekisa ukuthi kukhona yini i-XXY pair noma cha.

Ngaphezu kwalokhu kuhlolwa, emadodeni amadala, udokotela futhi anga-oda ezinye izivivinyo ezinjengokuhlolwa kwamahomoni noma ikhwalithi yesidoda, ukusiza ukuqinisekisa ukuxilongwa.

Yelashwa kanjani

Alikho ikhambi le-Klinefelter syndrome, kepha udokotela wakho angakweluleka ukuthi ungene esikhundleni se-testosterone ngemijovo esikhunjeni noma ngokufaka amabala, akhipha i-hormone kancane ngokuhamba kwesikhathi.

Ezimweni eziningi, le ndlela yokwelashwa iba nemiphumela engcono lapho iqala ebusheni, njengoba kuyisikhathi lapho abafana bethuthukisa khona izici zabo zocansi, kepha kungenziwa nakwabantu abadala, ikakhulukazi ukunciphisa ezinye izici ezinjengosayizi wamabele noma iphimbo eliphakeme lezwi.

Ezimweni lapho kunokulibaziseka kokuqonda, kungakuhle ukuthi uthole ukwelashwa nabachwepheshe abafanele kakhulu. Isibonelo, uma kunobunzima bokukhuluma, kungakuhle uthintane nodokotela wezinkulumo, kepha lolu hlobo lokulandelela lungaxoxwa nodokotela wezingane.