Wetin na Tripul X Sindrom? Lɛ wi tɔk bɔt dis sik we nɔ kin apin so ɔltɛm

Wi ɔl gɛt sɔntin we dɛn kɔl ‘kromozom’ insay di sɛl dɛn na wi bɔdi. Tink bɔt dɛn as di bluprint fɔ wi bɔdi. כltin frכm wi ayt to wi yay kכla to di tεkschכr fכ wi ia, na di jin dεm we de na dεn kromozom dεm ya de sho. nכmal wan, uman gεt tu ‘X’ kromozom dεm, εn man gεt wan ‘X’ εn wan ‘Y’. bכt rili sכmtεm dεn kin bכn sכm gyal pikin dεm wit εkstra ‘X’ kromozom. Dat na di jεnεtik kכndishכn we wi kכl Triple X Syndrome, כ 47,XXX. Nɔr de ala wae yu yɛri dis, bɔrku tɛm i nɔr kin siriɔs. Lɛ wi tɔk bɔt dis ditayli.

Wetin mek dis de apin? Wetin na di rizin fɔ dis?

Fɔ tɔk am simpul wan, triplɛ X sindrom na tin we kin apin ɔltɛm . Nɔto ɛnibɔdi in fɔlt. di ekstra X kromozom dεn de ad biכs fכ sכm mistek we de na di sεl divεlכpmεnt na di mama in eg כ di papa in sεl dεm we dεn bכn pikin. כ i kin apin we di sεl dεm de divεlכp ali we di εmbrayo de divεlכp.

Pan ɔl we dɛn dɔn si se di risk fɔ dis sik kin bɔku smɔl pan gyal pikin dɛn we mama dɛn we dɔn pas 35 ia bɔn, dɛn kin tek am se i nɔ kin apin so ɔltɛm we kin apin to mama dɛn we ol ɛni ej.

sכmtεm, dis εkstra X kromozom nכ de insay כl di sεl dεm na di bכdi. Na sɔm sɛl dɛn nɔmɔ i de insay. dis min se sכm sεl dεm na nכmal (XX), we כda sεl dεm na (XXX). Insay mɛrɛsin, wi kin kɔl dis ‘mosaic’ kɔndishɔn.

Wetin na di sayn dɛm fɔ dis sik?

Na dis ples bɔku pipul dɛn kin sɔprayz. Bɔrku tɛm, gyal pikin ɛn uman dɛm wae gɛt triple X syndrome nɔr kin gɛt ɛni klia simptom , ɔr kin gɛt sɔm kayn sik wae nɔr kin pasmak. Na dat mek dɛn kin se na wan pan ɛvri tɛn pipul dɛm wae gɛt dis sik kin gɛt dis sik. Bɔrku pipul dɛn kin liv nɔrmal, wɛl bɔdi layf ɛn nɔr kin ivin no se dɛn gɛt dis sik.

Bɔt sɔm pipul dɛn kin gɛt sɔm sayn dɛn. Dɛn sayn ya kin difrɛn frɔm wan pɔrsin to ɔda pɔrsin. Lɛ wi put dɛn sayn dɛn de na difrɛn difrɛn say dɛn.

Jɔs bikɔs yu pikin gɛt wan ɔ mɔ pan dɛn sik ya nɔ min se i gɛt triplɛ X sindrom. Bɔrku ɔda tin kin kam wit dɛn, so if yu gɛt ɛnitin fɔ wɔri bɔt, i go fayn fɔ mek yu tɔk to dɔktɔ.

Aw yu no dis sik?

Bɔrku tɛm, dɛn kin no dis sik bay wan. fכ egzampl, dεn kin no we uman de go fכ tritmεnt fכ wan prכblεm lεk fכ fεtiliti prכblεm כ fכ mεnopos kwik.

Ɔda we dɛn we dɛn kin du am na:

• Tεst dεm we dεn kin du we uman bεlε: Jεnεtik tεst dεm lεk NIPT (Non-Invasive Prenatal Testing) , Amniocentesis , כ CVS (Chorionic Villus Sampling) we dεn du pan mama we gεt bεlε kin no dis kכndyushכn bifo dεn bכn di pikin.
• Blɔd tɛst: Afta dɛn bɔn di pikin, if di dɔktɔ gɛt ɛni dawt, dɛn kin du karyotayp tɛst fɔ kɔnfirm dis. dis tεst kin no if di εkstra X kromozom de εn us pasεnshכn pan di sεl dεm i de insay.

Wetin na di tritmɛnt dɛm fɔ dis?

Di fɔs tin fɔ mɛmba na dat di jenɛtik kɔndishɔn we dɛn kɔl Triple X Syndrome nɔ go ebul fɔ wɛl ɔl.Na bikɔs na sɔntin we kin kam wit wi jin. Bɔt if yu sɔpɔt ɛn manej di prɔblɛm ɛn sayn dɛm we i kin kam wit, yu kin liv nɔmal layf ɛn gladi at .

Dɛn kin no aw fɔ trit ɛnibɔdi in sayn ɛn wetin i nid.

• Yu fɔ chɛk yu dɔktɔ ɔltɛm: Yu dɔktɔ kin tɛl yu fɔ du tɛst lɛk ɔltra saund skan ɛn ɛkokadiogram (EKG) fɔ chɛk if yu gɛt ɛni prɔblɛm wit yu kidni, ovaria, ɛn at.
• Sɔpɔt savis ɛn tritmɛnt dɛm: Dis na di pat we impɔtant pas ɔl.
• Tɛrapi fɔ tɔk ɛn langwej: Dis rili impɔtant fɔ pikin dɛn we nɔ de tɔk fayn.
• Fɔ trit yu bɔdi: I kin ɛp if yu gɛt mɔsul dɛn we wik ɔ yu gɛt prɔblɛm wit yu balans.
• Ɛdyukeshɔn sɔpɔt: Dɛn kin gi pikin dɛn we gɛt disabiliti fɔ lan spɛshal sɔpɔt na skul.
• Kɔnsul: Kɔnsul kin rili fayn fɔ dil wit wɔri, pwɛl hat, ɔr prɔblɛm wit sɔshal rileshɔnship.
• Ɔmon tɛrapi: Sɔntɛnde, di dɔktɔ kin tɛl am tin dɛn lɛk ɛstrojen tɛrapi fɔ trit prɔblɛm dɛn we kin kam bikɔs di ovarian nɔ de wok fayn ɔ fɔ kɔntrol di pikin in ayt.

Di tin we impɔtant pas ɔl na fɔ no dis sik kwik kwik wan ɛn gi di pikin di sɔpɔt ɛn tritmɛnt we i nid so dat di pikin go ebul fɔ du ɔl wetin i ebul fɔ du.