Ungayibona kanjani futhi uyiphathe kanjani i-Aase-Smith syndrome

-Delile

• Yelashwa kanjani
• Yini engadala le syndrome
• Ukuxilongwa kwenziwa kanjani

I-Aase syndrome, eyaziwa nangokuthi i-Aase-Smith syndrome, yisifo esingajwayelekile esidala izinkinga ezifana nokushoda kwegazi njalo nokungasebenzi kahle emajoyintini nasemathanjeni ezingxenye ezahlukahlukene zomzimba.

Okunye kokukhubazeka okuvame kakhulu kufaka:

• Amalunga, iminwe noma izinzwane, okuncane noma okungekho;
• Ulwanga olucwebile;
• Izindlebe ezikhubazekile;
• Ukujikisa izinkophe;
• Kunzima ukwelula ngokugcwele amalunga;
• Amahlombe amancane;
• Isikhumba esikhanyayo kakhulu;
• Ilunga lihlangane izithupha.

Le syndrome ivela ekuzalweni futhi yenzeka ngenxa yokuguquka okungahleliwe kwezakhi zofuzo ngesikhathi sokukhulelwa, yingakho, ezimweni eziningi, kuyisifo esingelona ifa. Kodwa-ke, kunezimo ezithile lapho lesi sifo singadlula sisuke kubazali siye ezinganeni.

Yelashwa kanjani

Ukwelashwa kuvame ukukhonjiswa ngudokotela wezingane futhi kufaka ukumpontshelwa igazi ngonyaka wokuqala wokuphila ukusiza ukulawula i-anemia. Kuyo yonke le minyaka, i-anemia isinciphile kakhulu, ngakho-ke, ukumpontshelwa igazi kungabe kungasadingeki, kepha kuyalulekwa ukuthi kuhlolwe igazi kaningi ukuhlola amazinga amaseli abomvu egazi.

Ezimweni ezinzima kakhulu, lapho kungenzeki khona ukulinganisela amazinga abomvu egazi nokumpontshelwa igazi, kungahle kudingeke ukufakelwa umnkantsha wethambo. Bona ukuthi kwenziwa kanjani lokhu kwelashwa nokuthi ziyini izingozi.

Ukukhubazeka akuvamile kudinga ukwelashwa, ngoba kungaphazamisi imisebenzi yansuku zonke. Kepha uma lokhu kwenzeka, udokotela wezingane angancoma ukuhlinzwa ukuzama ukwakha kabusha indawo ethintekile nokubuyisela ukusebenza.

Yini engadala le syndrome

I-Aase-Smith syndrome ibangelwa ushintsho kwesinye sezakhi zofuzo ezibaluleke kakhulu ekwakheni amaprotheni emzimbeni. Lolu shintsho luvame ukwenzeka ngokungahleliwe, kepha ezimweni ezingavamile kakhulu lungadlula lusuke kubazali luye ezinganeni.

Ngakho-ke, lapho kunezimo zalesi sifo, kuhlala kunconywa ukuthi uthintane nokwelulekwa ngezakhi zofuzo ngaphambi kokukhulelwa, ukuthola ukuthi iyini ingozi yokuba nezingane ezinesifo.

Ukuxilongwa kwenziwa kanjani

Ukuxilongwa kwalesi sifo kungenziwa udokotela wezingane kuphela ngokubheka ukungasebenzi kahle, noma kunjalo, ukuqinisekisa ukuxilongwa, udokotela anga-oda i-bone marrow biopsy.

Ukuhlonza uma kune-anemia ehambisana ne-syndrome, kuyadingeka ukuthi kuhlolwe igazi ukuhlola inani lamaseli abomvu egazi.