Wetin na di sik we dɛn kɔl Klinefelter Syndrome? Lɛ wi tɔk bɔt am simpul wan.

As mama ɔ papa, sɔntɛnde yu kin gɛt sɔm kwɛstyɔn ɔ wɔri bɔt aw yu bɔy pikin de gro. I tan lɛk se i lɔng pas ɔda pikin dɛn fa fawe? Ɔ i tan lɛk se i dɔn let fɔ bɔn? Ɔ i gɛt sɔm prɔblɛm dɛn fɔ lan? Di tin we kin mek dɛn tin ya apin kin bi wan sik we yu gɛt we yu nɔ ɛva yɛri bɔt bifo. Wan pan dɛn kayn sik ya, bɔt nɔr kin bɔku, dɛn kɔl am Klinefelter Syndrome.

Fɔ tɔk am simpul wan, wetin na Klinefelter Syndrome?

Okay, mek wi tek smɔl ɛgzampul fɔ ɔndastand dis. Imajin se wi bɔdi tan lɛk big buk we gɛt bɔku instrɔkshɔn dɛn. Di chapta dɛn na dis buk na wetin wi kɔl kromozom. Insay dɛn kromozom ya, wi gɛt wi jin dɛn, we na di instrɔkshɔn dɛn we de sho ɔltin frɔm wi ayt, kɔlɔ, ɛn aw wi ia tan.

nכmal wan, εvri sεl na man in bכdi gεt 46 pan dεn kromozom dεm ya. Tu pan dɛn tin ya de sho mami ɛn dadi biznɛs. Dɛn na wan X kromozom ɛn wan Y kromozom. Wi de kol dis 46, XY fo shot.

Naw, dis patɛn difrɛn smɔl fɔ pɔrsin wae gɛt Klinefelter Syndrome. Dɛn sɛl dɛn kin gɛt ɛkstra X kromozom . Dat min se dɛn jenɛtik mek-ap na 47, XXY . Dis na wan sik we dɛn bɔn wit. Dat min se dɛn bɔn pɔsin wit dis sik.

Wetin na di sayn dɛm fɔ dis sik?

De sayn dɛm fɔ Klinefelter Syndrome kin difrɛn frɔm pɔrsin to ɔda pɔrsin. Sɔm pipul kin gɛt bɔrku sayn dɛm, ɛn ɔda wan dɛm nɔr kin gɛt ɛni sik wae de sho klia wan. Dis na di rizin we mek bɔku pipul dɛn nɔ kin no am. In jɛnɛral, dɛn kin sheb dɛn sik ya to tu men kategori.

Wetin mek dis de apin? Na ɛnibɔdi in fɔlt dis?

Dis na di kwɛstyɔn we impɔtant pas ɔl. Klinefelter Syndrome nɔto ɛni we na di mama ɔ di papa in fɔlt. Na wan chenj we kin apin na di jɛnɛtiks we nɔ kin apin ɔltɛm. i kin kכz fכ wan mistek we dεn kin mek we dεn de sheb di sεl dεm we kin apin we dεn bכn pikin.

Fɔ tɔk am simpul wan, tri men we dɛn de we dis kin apin:

• di prεsεns fכ wan εkstra X kromozom insay wan sεl sεl.
• di prεsεns fכ wan εkstra X kromozom insay wan eg.
• mistek kin apin we di sεl dεm divayd ali insay di εmbrayo. Dɛn kɔl dis `(mosaic Klinefelter syndrome)`. wetin de apin ya na dat na sכm pan di sεl dεm na di bכdi nכmכ gεt di εkstra X kromozom.

Aw fɔ no dis sik?

Bɔrku tɛm, dɛn kin no dis sik pan sɔm kayn kes dɛm.

• di tεm we di pikin de stej: dεn kin no dis insidεnt wan we dεn de du jεnεtik tεst (lεk amniocentesis) fכ כda rizin.
• We i smɔl: Dɔktɔ kin sɔprayz ɛn rifer di pikin fɔ tɛst bikɔs i nɔ de gro fayn (we i de tɔk, i nɔ ebul fɔ waka) ɔ i nɔ kin izi fɔ lan.
• we i yכng: dεn kin no am bikoz fכ כda abnכmal tin dεm (e.g. di brεst divεlכpmεnt, rεdכks di ia dεm we de gro) we i de bכn.
• We yu dɔn big:Bɔku tɛm dɛn kin no dis sik we pɔsin big we dɛn kin du tɛst fɔ no if pɔsin nɔ ebul fɔ bɔn pikin .

di men tεst fכ kכnfכm dis na karyotayp tεst . Dis na simpul blɔd tɛst. I kin chɛk di rayt nɔmba ɛn di kayn kromozom dɛn we de na yu ɔ yu pikin in sɛl dɛn.

If dɛn no se pikin gɛt dis sik, dɔktɔ dɛn kin tɛl am bak fɔ du nyurosaykolojik tɛst fɔ ɔndastand aw i de lan ɛn aw i de tink.

Wetin na di tritmɛnt dɛn? Yu tink se dɛn go ebul fɔ mɛn dis?

Bikɔs Klinefelter Syndrome na wan jɛnɛtik kɔndishɔn, i nɔ kin ebul fɔ "krɔs." Bɔt , i pɔsibul fɔ mek yu ebul fɔ kɔntrol di sik dɛn fayn fayn wan ɛn liv layf we nɔmal, gladi, ɛn gɛt wɛlbɔdi. Di men gol fɔ tritmɛnt na fɔ kɔntrol di sayn dɛm.

1. Ɔmon tɛrapi (Tɛstostɛron Riplesmɛnt Tɛrapi) .

Pipul dεm wae gεt dis kכndyushכn gεt lכw lεvεl כf di man כmon tεstostεron na dεn bכdi. So, dɔktɔ dɛn se yu fɔ gi yu tɛstostɛron na do we yu ol di rayt ej. Dɛn kin gɛt dis bay we dɛn de injɛkshɔn, jel, ɔ pat.

Di bɛnifit dɛn we dis tritmɛnt de gi:

• Fɔ mek di bon dɛn strɔng.
• Di mɔsul dɛn we de gro.
• Di ia we de gro na di fes ɛn bɔdi.
• Dip we di vɔys de dip.
• Impruv mental stet ɛn fɔ gɛt kɔnfidɛns pan insɛf.
• Di want fɔ du mami ɛn dadi biznɛs mɔ ɛn mɔ.

2. Difrɛn tritmɛnt tritmɛnt dɛm (Therapies) .

Dipen pan wetin di pikin nid, dɛn kin aks fɔ ɛp frɔm difrɛn tritmɛnt pipul dɛn.

• Speech-language pathologists: Ɛp wit di prɔblɛm dɛn we pɔsin kin tɔk.
• Di wan dɛn we de mɛn yu bɔdi: Ɛp fɔ mek yu mɔsul dɛn strɔng ɛn fɔ mek yu balans fayn fayn wan.
• Ɔkupeshɔn thɛrapist dɛm: Ɛp fɔ divɛlɔp di skil dɛm we yu nid fɔ du ɛvride wok izi wan.
• Saykolojik advays: De gi sɔpɔt to di pikin ɛn in famili fɔ bia wit strɛs ɛn wɔri we kin kam.

3. Ɔpreshɔn

Dis nɔ kin nid fɔ apin bɔku tɛm. Bɔt if pɔsin de gɛt bɔku prɔblɛm bikɔs in bɔdi de gro (gaynecomastia) afta i dɔn big, dɛn kin du ɔpreshɔn we i dɔn big fɔ pul di ɛkstra tisu.

Ustɛm yu fɔ go to yu dɔktɔ?

If yu na mama ɔ papa ɛn yu notis ɛnitin we de mek yu pikin de delay ɔ we nɔ de gro, tɔk to yu dɔktɔ we de mɛn pikin dɛn bɔt dat.

• If yu pikin de kray, waka, ɔ tɔk leta pas ɔda pikin dɛn we gɛt di sem ej.
• If yu yɔŋ bɔy pikin sho se in bɔdi nɔ de wok fayn (i leg lɔng, i de ay pasmak), ɔ i gɛt prɔblɛm wit aw i de lan ɔ aw i de biev.

If yu na big pɔsin ɛn i nɔ izi fɔ yu fɔ gɛt bɛlɛ ɔ yu gɛt ɛni ɔda sayn dɛn we wi dɔn tɔk bɔt, mek shɔ se yu tɔk to yu dɔktɔ bɔt am. No rizin nɔ de fɔ mek wi fred ɔ shem.

Na nɔmal tin fɔ fil frayd ɛn shɔk we yu lan bɔt wan jenɛtik kɔndishɔn lɛk Klinefelter Syndrome. Bɔt mɛmba se, if yu gi yu di rayt advays ɛn tritmɛnt, yu go ebul fɔ liv fayn fayn wan wit dis sik.