Yu no bɔt Triple X Syndrome? Lɛ wi tɔk bɔt am simpul wan.

Sɔntɛnde yu kin fil lɛk se yu gyal pikin lɔng pas ɔda pikin dɛn we in ej? Ɔ i tan lɛk se i de biɛn smɔl pan skul wok, ɔ i gɛt sɔm prɔblɛm fɔ pe atɛnshɔn? Sɔmtɛm, i kin bi se wan jenɛtik kɔndishɔn de biɛn dis we wi nɔ kin tɔk bɔt bɔku, bɔt i rili impɔtant fɔ no bɔt. Na dat na Triple X Syndrome. Nɔ fred we yu yɛri dis nem. I nɔto siriɔs sik. Tide, wi go tɔk bɔt ɔltin insay wan rili simpul we we yu go ɔndastand.

Fɔ tɔk am simpul wan, wetin na Triple X Syndrome?

Fɔ ɔndastand dis, wi fɔs nid fɔ no smɔl bɔt di kromozom dɛn we de na wi bɔdi. Tink bɔt wi bɔdi lɛk big buk we de tich wi. Dɛn rayt ɔl di tin dɛn we wi no, lɛk wi ayt, wi skin kɔlɔ, wi yay kɔlɔ, ɛn aw wi ia tan, na dis buk. Kromozom na di chapta dɛn na dis buk.

Nɔmal wan, ɛvri sɛl na mɔtalman bɔdi we gɛt wɛlbɔdi kin gɛt 23 pe pan dɛn kromozom ya, ɔ 46 kromozom dɛn. Wan pe pan dɛn tin ya de sho wi man ɔ uman.

• Uman dɛn gɛt tu X kromozom dɛn. Wi kɔl dat (XX) .
• Man dεm gεt wan X kromozom εn wan Y kromozom. Wi de kɔl am (XY) .

Naw yu ɔndastand? Ok. Triple X syndrome na wan sik we de afɛkt uman dɛn nɔmɔ. uman we gεt dis kכndyushכn gεt εkstra X kromozom insay כl in sεl dεm, כ insay sכm pan in sεl dεm, apat frכm di tu X kromozom dεm we nכmal fכ de (XX). dis min se dεn sεks kromozom dεm dεn arenj lεk (XXX) . Na dat mek dɛn kɔl am ‘triple X’.

sכmtεm, dis εkstra X kromozom kin de insay sכm sεl dεm nכmכ, nכto כl dεm. Insay mɛrɛsin, wi kin kɔl dis mosayk kɔndishɔn.

Aw dis sik kin kɔmɔn?

Dis na rili wan sik we nɔ kin apin so ɔltɛm. Risach dɔn sho se i kin afɛkt lɛk wan pan ɛvri 900 to 1,000 gyal pikin dɛn we dɛn jɔs bɔn.

Bɔt de impɔtant tin ya na dat bɔrku pipul dɛm wae gɛt dis sik nɔr kin sho ɛni sayn. Dɛn de liv nɔmal, wɛlbɔdi layf. So, dɛn nɔ kin ɛva ivin no se dɛn gɛt dis chenj na dɛn jɛnɛtiks. Fɔ dis rizin, dɔktɔ dɛn biliv se di rial nɔmba fɔ pipul dɛn we gɛt dis sik kin bɔku pasmak.

Wetin na di sayn dɛm fɔ Triple X syndrome?

Dis na sɔntin we bɔku mama ɛn papa dɛn want fɔ no. Mɛmba se, de sayn dɛm kin difrɛn frɔm wan pɔrsin to ɔda pɔrsin wae gɛt dis sik. Sɔm pipul dɛn nɔ kin fil natin atɔl. Ɔda pipul dɛn kin sho smɔl smɔl sayn dɛm fɔ wan ɔr mɔr pan dɛn tin ya:

Lɛ wi sheb dɛn tin ya to pat dɛn fɔ mek i izi fɔ ɔndastand.

Wetin na di rizin fɔ dis? Dis na sɔntin we pipul dɛn kin pas fɔ lɔng lɔng tɛm?

Dis na prɔblɛm we bɔku pipul dɛn gɛt. Triple X syndrome na wan sik wae de kam wit jεnεtiks, bɔt nɔr kin gɛt am frɔm di mama ɛn papa. I kin apin klos to ɔltin bay chans.

Fɔ tɔk am simpul wan, we dɛn mek pikin frɔm in mama in eg sɛl ɛn in papa in swɛlin sɛl, smɔl mistek kin apin na di kromozom dɛn we dɛn sɛl dɛn de sheb. dis mistek de mek dεn ad wan εkstra X kromozom. Dis nɔto bikɔs ɔf ɛnibɔdi in fɔlt.

Risach dɔn sho se di risk fɔ dis sik kin go ɔp smɔl if di mama dɔn pas 35 ia di tɛm we i gɛt bɛlɛ. Bɔt dis nɔ min se ɔlman we pas 35 ia gɛt dis prɔblɛm.

Aw dɛn kin no se pɔsin gɛt Tripul X sindrom?

As wi bin dɔn tɔk, bikɔs bɔku pipul dɛn nɔ kin gɛt ɛni sayn fɔ dis sik, dɛn nɔ kin no bɔt dis sik. Bɔt if dɔktɔ tink se di pikin nɔ de gro fayn ɔ i nɔ ebul fɔ lan, dɛn kin sɛn am fɔ mek dɛn go tɛst am in jɛnɛtiks.

• Jɛnɛtik tɛst: Di men tɛst we dɛn kin yuz fɔ dis na wan blɔd tɛst we dɛn kɔl karyotype . Dis kin mek yu si klia wan di nɔmba ɛn shep fɔ di kromozom dɛn we de na di blɔd sɛl dɛn.
• bεlε tεst: sכmtεm tεst dεm we dεn du fכ כda rizin dεm we uman bεlε (e.g. NIPT, Amniocentesis, CVS) kin gi wan klyu bכt dis kכndyushכn. Bɔt ivin if yu no sɔntin lɛk dat, i rili impɔtant fɔ mek yu du tɛst bak afta dɛn bɔn di pikin fɔ mek yu kɔnfɔm am.
• Ɔda kes dɛm: Sɔm uman dɛn kin no se dɛn gɛt dis sik tru tɛst we dɛn de fɛn tritmɛnt fɔ di prɔblɛm dɛn we gɛt fɔ du wit di we aw dɛn de bɔn pikin.

Wetin na di tritmɛnt dɛm fɔ dis?

We a yɛri dis, di fɔs tin we kin kam na mi maynd na, "Dɛn kin mɛn dis?"

Fɔ no am kwik kwik wan na di men tin. If dɛn no se pikin gɛt dis sik kwik kwik wan, dɛn kin gɛt di sɔpɔt ɛn tritmɛnt we dɛn nid kwik kwik wan.

Bɔku tɛm, di dɔktɔ kin tɔk bɔt tin dɛn lɛk:

• Renal Ultrasound: Fɔ chɛk fɔ ɛni abnɔmal tin na di kidni.
• Di advays we dɔktɔ we de mɛn di at kin gi: Chɛk aw di at de wok.
• Fizik Tɛrapi: If di mɔsul dɛn wik, mek dɛn strɔng ɛn mek dɛn ebul fɔ muv fayn fayn wan.
• Ɔkupeshɔn Tɛrapi:Divɛlɔp di skil dɛm we yu nid fɔ du ɛvride wok izi wan (lɛk fɔ drɛs, rayt, ɛn ɔda tin dɛm).
• Spich Therapy: Ɛp fɔ tɔk delay ɔ fɔ gɛt prɔblɛm wit yu langwej.
• Ɛdyukeshɔn sɔpɔt: Fɔ gi spɛshal atɛnshɔn ɛn sɔpɔt na skul to pikin dɛn we gɛt disabiliti fɔ lan.
• Saikɔlɔjik advays: If tin de lɛk fɔ wɔri ɔr nɔr gɛt kɔnfidɛns pan insɛf, ɛp dɛn fɔ bia wit dɛn.
• Masta sabi pipul dɛn advays bɔt aw fɔ bɔn pikin: Gɛt di advays we yu nid we yu de plan fɔ mek famili tumara bambay.

Aw layf de wit dis sik? Yu tink se i kin afɛkt di layf we pɔsin de liv?

Dis na di fayn tin we wi fɔ no. Bɔrku pan pipul dɛm wae gɛt triple X syndrome de liv kɔmplit nɔrmal, wɛl bɔdi, ɛn gladi layf. Dɛn kin go skul, gɛt ay edyukeshɔn, gɛt wok, mared, ɛn bɔn pikin dɛn.

Dis sik nɔr kin afɛkt pɔrsin in layf pan ɛni we. Bɔku tɛm, dɛn kin liv lɔng lɛk ɔda uman dɛn. Ɔl wetin dɛn nid na fɔ intavyu kwik ɛn gi di sɔpɔt we nid if ɛnitin de we nɔ izi fɔ yu.

As mama ɔ papa, na nɔmal tin fɔ mek yu fred ɛn wɔri we yu kam fɔ no se yu pikin gɛt dis sik. I kin bi rilif bak fɔ fɛn rizin fɔ prɔblɛm we dɔn de mɔna yu fɔ lɔng tɛm, lɛk, "Oh... na dat mek i tan lɛk dis." Ɔl dɛn filin ya na nɔmal tin. Di impɔtant tin na fɔ no se nɔto yu wangren de. Tɔk opin wan bɔt dis wit yu dɔktɔ. I kin gi yu infɔmeshɔn bak bɔt sɔpɔt grup ɛn ɔda tin dɛn we go ɛp yu.