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Wetin na Triploidy? As mama we gɛt bɛlɛ, yu no bɔt dis?

Wetin na Triploidy? As mama we gɛt bɛlɛ, yu no bɔt dis?

Bɛlɛ na tɛm we ɔl mama kin gɛt bɔku op ɛn bak sɔm tin dɛn we i kin fred. So, insay dis tεm, wi kin tink כltεm bכt di pikin in bεlε in hεlth. Tide wi go tɔk bɔt wan sik we nɔ kin apin so ɔltɛm we bɔku pipul dɛn nɔ yɛri bɔt, bɔt i impɔtant fɔ no. Dat na Triploidy. dis na kכndyushכn we kin afekt bitwin 1% εn 3% pan di bεlε.

Wetin na triploidy insay simpul wɔd dɛn?

Okay, lɛ wi bigin bay we wi ɛksplen dis simpul wan. Ɛvri sɛl na wi bɔdi gɛt wi jɛnɛtik infɔmeshɔn, we na smɔl smɔl tin dɛn we de sho ɔltin frɔm wi ayt to wi skin kɔlɔ to wi yay kɔlɔ. Wi kin kɔl dɛn kromozom ya .

Nɔmal wan, pɔsin we gɛt wɛlbɔdi kin gɛt 46 kromozom dɛn na in bɔdi. Dɛn arenj dɛn insay 23 tu tu. Wi kin gɛt 23 pan dɛn frɔm wi mama ɛn di ɔda 23 frɔm wi papa. Dis na di nɔmal tin we kin apin.

Bɔt insay wan kɔndishɔn we dɛn kɔl triploidy , insted ɔf dɛn 46 kromozom ya, dɛn kin ad wan ɛkstra sɛt fɔ kromozom , we kin mek di ɔl nɔmba rich 69. Imajin, i tan lɛk se yu ad wan ɛn af tɛm di nɔmal nɔmba. Dis ekstra jεnεtik infכmeshכn kin rili afekt di pikin in divεlכpmεnt.

Wetin na di rizin we mek dis kayn tin de apin?

Bɔku mama ɛn papa dɛn kin wɔnda if na dɛn fɔlt we sɔntin lɛk dis apin. Bɔt yu fɔ no se triploidy nɔto ɛnibɔdi in fɔlt. Na wan rili rare coincidence we kin apin di moment we pikin geht bɛlɛ.

nכmal wan, pikin kin fכm we wan sεl εn wan eg jɔyn. Bɔt insay triplɔi, dɛn tin ya kin apin:

  • wan nכmal eg de fεtilayz wan tεm bay tu sεl dεm .
  • fεtilayzכn fכ nכmal eg bay wan sεl we gεt εkstra sεt fכ kromozom dεm (difεktiv).
  • nכmal sεl de fεtilayz wan eg wit εkstra sεt fכ kromozom dεm (difεktiv).

Ɛnitin de we kin mek dis sik apin?

Di masta sabi pipul dɛm nɔr dɔn ebul fɔ fɛn ɛni patikyula risk factor fɔ dis yet. I nɔto sik we pɔsin kin gɛt frɔm in mama ɛn papa. Ɛn nɔto di ej we di mama ɔ papa gɛt. Risach dɔn sho se if yu dɔn gɛt am wan tɛm, di chans fɔ mek i apin bak insay yu nɛks bɛlɛ rili smɔl.

Aw triploidy kin afɛkt di pikin ɛn mama

We wi de tɔk bɔt dis sityueshɔn, wi nid fɔ pe atɛnshɔn pan tu tin dɛn: wan na di impak we i gɛt pan di pikin we nɔ bɔn yet, ɛn di ɔda wan na di impak we i gɛt pan di mama we gɛt bɛlɛ.

Prɔblɛm dɛn we kin apin to di pikin

If bɛlɛ wit dis sik go bifo ɛn bɔn pikin (we nɔ kin apin so ɔltɛm), di pikin kin gɛt siriɔs wɛlbɔdi prɔblɛm ɛn bɔku prɔblɛm dɛn we i kin bɔn.

Pat we dɛn afɛkt Prɔblɛm ɛn sayn dɛn we kin apin
Di ɔgan dɛn we de insay di bɔdi Siriɔs prɔblɛm wit di at, di bren divɛlɔpmɛnt, di kidni, di spayna, di liva, ɛn di gal blad.
Aw a luk di yay dεm we de fa fawe, wan lכw brij na di nos, di ia lכb dεm we de lכs pas nכmal εn gεt difrεn shep, sכm sכm chin, sכl lip εn palata, finga dεm εn fut dεm we fכs tכgeda, εn layn dεm we nכ kɔmɔn na di palm dεm.

Di tin dɛn we kin apin to di mama we gɛt bɛlɛ

bכku tεm, bεlε we gεt triploidy go bכn insay di fכs mכnt dεm. bikɔs ɔf dis bad bad tin we nɔ de apin na di bɔdi, di bɔdi kin jɔs dɔn di bɛlɛ .

Bɔt i nɔ kin apin so ɔltɛm, if di bɛlɛ go bifo, di mama kin gɛt wan bad bad sik we dɛn kɔl prɛeklampsia .

Pri-ɛklamsia na siriɔs sik we de sho se yu gɛt ay blɔd prɛshɔn. Yu fɔ rili tek tɛm wit dɛn sayn ya:

  • Di an, fut, ɔ fes we de swel (ɛdima) .
  • di wet we yu de gεt wan wan we pas 3-5 paund insay sכm tεm, lεk wan wik
  • Di ed we kin at bad bad wan bɔku tɛm
  • Diziz ɛn blu yay
  • I nɔ kin izi fɔ yu fɔ blo
  • Di urine we de kɔmɔt na di bɔdi dɔn go dɔŋ
  • Di pen we de na di ɔp pat na di bɛlɛ
  • Nɔs ɔ vɔmit
  • Flash bifo di yay, blurred vision

Dɛn sayn ya kin apin bak pan ɔda mɛrɛsin, so if yu gɛt ɛni wan pan dɛn sayn ya , yu fɔ go to yu dɔktɔ wantɛm wantɛm. If dɛn nɔ trit am, prɛ-ɛklampsia kin kil di mama ɛn di pikin.

Aw fɔ no dis sik?

We dɛn de du ɔltrasɔund skan we dɛn kin du ɔltɛm we uman gɛt bɛlɛ, di dɔktɔ kin sɔprayz se dis. dis sכspεshכn kin kam bikoz di pikin de gro sloslo, lכw amniotic fluid na di uterus, כ abnכmal tin dεm na di pikin in bכdi.

Fɔ mek dɛn no di pɔsin we dɛn de tink, dɛn fɔ tɛst di pikin in kromozom dɛn. Tu tɛst dɛn de fɔ dis:

1. Amniocentesis: dis involv fכ pas wan nidul we rili tכn tru yu bכdi, tek sכm sכm sכm sεmpl fכ di amniotic fluid we de rawnd di pikin, εn tεst di pikin in kromozom dεm na di sεl dεm.

2. Chorionic villus sampling (CVS): dis involv fכ tek wan sכm pat pan di plasεnta εn egzamin am.

Bikɔs i nɔ kin izi fɔ mek uman gɛt bɛlɛ wit dɛn tu tɛst ya, i impɔtant fɔ tɔk gud gud wan wit yu dɔktɔ bɔt di gud ɛn bad tin dɛn bifo yu disayd fɔ du sɔntin.

afta dεn bכn pikin, dεn kin kכnfכm dis bay we dεn tek sεmpl fכ di pikin in skin εn tεst di kromozom dεm.

Aw di tritmɛnt ɛn aw fɔ si am tan lɛk?

Bɔt i sɔri fɔ no se, no mɛrɛsin nɔ de fɔ mek pɔsin gɛt triplɔyd. I nɔ go ebul fɔ mɛn am. If dɛn bɔn pikin wit dis sik, di mɛdikal tim go jɔs gi sɔpɔt kia we dɛn de trit di pikin in sik dɛn.

bikɔs ɔf dis, bɔku pan di pikin dɛn we dɛn bɔn wit triplɔdi kin day insay sɔm dez ɔ mɔnt afta dɛn bɔn dɛn.

Bɔt, dɛn nɔ kin rili ripɔt bɔt pipul dɛn we dɔn liv te dɛn big. Dɛn gɛt wan spɛshal sik we dɛn kɔl mosaic triploidy . dis min se sכm sεl dεm na dεn bכdi gεt di nכmal 46 kromozom dεm, we כda wan dεm gεt כnli 69. bכt dεn kin gεt siriכs prכblεm dεm bak lεk fכ divεlכpmεnt delay, disabiliti fכ lan, εn sεiz.

Triploidy ɛn Trisomy na di sem tin?

Yɛs. Pan ɔl we dɛn tu nem ya kin tan lɛk di sem we we yu yɛri dɛn, dɛn tu nem ya na tu difrɛn tin dɛn.

  • triploidy na di adishכn fכ wan komplit εkstra sεt fכ kromozom dεm (23+23+23 = 69).
  • Trisomy na we yu ad jכs wan kromozom to wan nכmal pe kromozom. fכ egzampl, Down syndrome na wan kכndyushכn we dεn kכl ‘trisomy 21’. dis min se dεn ad εkstra kromozom to di 21st pe, we de mek di pe tri.

We ɛni mama ɔ papa lan bɔt dis kayn tin we kin mek i fil bad. So, i rili impɔtant fɔ gɛt di mɛrɛsin advays ɛn sɔpɔt we yu nid fɔ gɛt pan yu maynd.

Mɛsej we dɛn kin kɛr go na os

  • triploidy na di kromozom abnכmaliti we de apin randomly we uman de bכn. Nɔto ɛnibɔdi in fɔlt.
  • Dis sik kin dɔn bɔku tɛm we uman kin gɛt bɛlɛ we i bigin.
  • If yu gɛt ɛni ɔda tin we nɔ kɔmɔn we yu gɛt bɛlɛ (espɛshali di sayn dɛm we de sho se yu gɛt prɛ-ɛklampsia) , go to yu dɔktɔ wantɛm wantɛm.
  • No mɛrɛsin nɔ de fɔ dis sik, ɛn we dɛn dɔn bɔn pikin, na di kia nɔmɔ dɛn kin gi di pɔsin we gɛt di sik.
  • Saikɔlɔjik sɔpɔt rili impɔtant fɔ mama ɛn papa dɛm wae de go tru dis ɛkspiriɛns, so nɔr frayd fɔ tɔk bɔt am wit yu dɔktɔ, fambul, ɛn pipul dɛm wae yu lɛk.

Triploidy, bεlε, kromozom, miskεri, prεeklampsia, bכn difεkt, jεnεtik sik dεm

Frequently Asked Questions (FAQ)

Triploidy ɛn Trisomy na di sem tin?

Yɛs. Pan ɔl we dɛn tu nem ya kin tan lɛk di sem we we yu yɛri dɛn, dɛn tu nem ya na tu difrɛn tin dɛn.

⚠️ Important: The medical articles and information on Nirogi Lanka are for general awareness only, and are by no means a substitute for professional medical advice, diagnosis, or treatment. For any medical problem you have, consult a qualified physician immediately.

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Wetin na Triploidy? As mama we gɛt bɛlɛ, yu no bɔt dis?

Wetin na Triploidy? As mama we gɛt bɛlɛ, yu no bɔt dis?

Bɛlɛ na tɛm we ɔl mama kin gɛt bɔku op ɛn bak sɔm tin dɛn we i kin fred. So, insay dis tεm, wi kin tink כltεm bכt di pikin in bεlε in hεlth. Tide wi go tɔk bɔt wan sik we nɔ kin apin so ɔltɛm we bɔku pipul dɛn nɔ yɛri bɔt, bɔt i impɔtant fɔ no. Dat na Triploidy. dis na kכndyushכn we kin afekt bitwin 1% εn 3% pan di bεlε.

Wetin na triploidy insay simpul wɔd dɛn?

Okay, lɛ wi bigin bay we wi ɛksplen dis simpul wan. Ɛvri sɛl na wi bɔdi gɛt wi jɛnɛtik infɔmeshɔn, we na smɔl smɔl tin dɛn we de sho ɔltin frɔm wi ayt to wi skin kɔlɔ to wi yay kɔlɔ. Wi kin kɔl dɛn kromozom ya .

Nɔmal wan, pɔsin we gɛt wɛlbɔdi kin gɛt 46 kromozom dɛn na in bɔdi. Dɛn arenj dɛn insay 23 tu tu. Wi kin gɛt 23 pan dɛn frɔm wi mama ɛn di ɔda 23 frɔm wi papa. Dis na di nɔmal tin we kin apin.

Bɔt insay wan kɔndishɔn we dɛn kɔl triploidy , insted ɔf dɛn 46 kromozom ya, dɛn kin ad wan ɛkstra sɛt fɔ kromozom , we kin mek di ɔl nɔmba rich 69. Imajin, i tan lɛk se yu ad wan ɛn af tɛm di nɔmal nɔmba. Dis ekstra jεnεtik infכmeshכn kin rili afekt di pikin in divεlכpmεnt.

Wetin na di rizin we mek dis kayn tin de apin?

Bɔku mama ɛn papa dɛn kin wɔnda if na dɛn fɔlt we sɔntin lɛk dis apin. Bɔt yu fɔ no se triploidy nɔto ɛnibɔdi in fɔlt. Na wan rili rare coincidence we kin apin di moment we pikin geht bɛlɛ.

nכmal wan, pikin kin fכm we wan sεl εn wan eg jɔyn. Bɔt insay triplɔi, dɛn tin ya kin apin:

  • wan nכmal eg de fεtilayz wan tεm bay tu sεl dεm .
  • fεtilayzכn fכ nכmal eg bay wan sεl we gεt εkstra sεt fכ kromozom dεm (difεktiv).
  • nכmal sεl de fεtilayz wan eg wit εkstra sεt fכ kromozom dεm (difεktiv).

Ɛnitin de we kin mek dis sik apin?

Di masta sabi pipul dɛm nɔr dɔn ebul fɔ fɛn ɛni patikyula risk factor fɔ dis yet. I nɔto sik we pɔsin kin gɛt frɔm in mama ɛn papa. Ɛn nɔto di ej we di mama ɔ papa gɛt. Risach dɔn sho se if yu dɔn gɛt am wan tɛm, di chans fɔ mek i apin bak insay yu nɛks bɛlɛ rili smɔl.

Aw triploidy kin afɛkt di pikin ɛn mama

We wi de tɔk bɔt dis sityueshɔn, wi nid fɔ pe atɛnshɔn pan tu tin dɛn: wan na di impak we i gɛt pan di pikin we nɔ bɔn yet, ɛn di ɔda wan na di impak we i gɛt pan di mama we gɛt bɛlɛ.

Prɔblɛm dɛn we kin apin to di pikin

If bɛlɛ wit dis sik go bifo ɛn bɔn pikin (we nɔ kin apin so ɔltɛm), di pikin kin gɛt siriɔs wɛlbɔdi prɔblɛm ɛn bɔku prɔblɛm dɛn we i kin bɔn.

Pat we dɛn afɛkt Prɔblɛm ɛn sayn dɛn we kin apin
Di ɔgan dɛn we de insay di bɔdi Siriɔs prɔblɛm wit di at, di bren divɛlɔpmɛnt, di kidni, di spayna, di liva, ɛn di gal blad.
Aw a luk di yay dεm we de fa fawe, wan lכw brij na di nos, di ia lכb dεm we de lכs pas nכmal εn gεt difrεn shep, sכm sכm chin, sכl lip εn palata, finga dεm εn fut dεm we fכs tכgeda, εn layn dεm we nכ kɔmɔn na di palm dεm.

Di tin dɛn we kin apin to di mama we gɛt bɛlɛ

bכku tεm, bεlε we gεt triploidy go bכn insay di fכs mכnt dεm. bikɔs ɔf dis bad bad tin we nɔ de apin na di bɔdi, di bɔdi kin jɔs dɔn di bɛlɛ .

Bɔt i nɔ kin apin so ɔltɛm, if di bɛlɛ go bifo, di mama kin gɛt wan bad bad sik we dɛn kɔl prɛeklampsia .

Pri-ɛklamsia na siriɔs sik we de sho se yu gɛt ay blɔd prɛshɔn. Yu fɔ rili tek tɛm wit dɛn sayn ya:

  • Di an, fut, ɔ fes we de swel (ɛdima) .
  • di wet we yu de gεt wan wan we pas 3-5 paund insay sכm tεm, lεk wan wik
  • Di ed we kin at bad bad wan bɔku tɛm
  • Diziz ɛn blu yay
  • I nɔ kin izi fɔ yu fɔ blo
  • Di urine we de kɔmɔt na di bɔdi dɔn go dɔŋ
  • Di pen we de na di ɔp pat na di bɛlɛ
  • Nɔs ɔ vɔmit
  • Flash bifo di yay, blurred vision

Dɛn sayn ya kin apin bak pan ɔda mɛrɛsin, so if yu gɛt ɛni wan pan dɛn sayn ya , yu fɔ go to yu dɔktɔ wantɛm wantɛm. If dɛn nɔ trit am, prɛ-ɛklampsia kin kil di mama ɛn di pikin.

Aw fɔ no dis sik?

We dɛn de du ɔltrasɔund skan we dɛn kin du ɔltɛm we uman gɛt bɛlɛ, di dɔktɔ kin sɔprayz se dis. dis sכspεshכn kin kam bikoz di pikin de gro sloslo, lכw amniotic fluid na di uterus, כ abnכmal tin dεm na di pikin in bכdi.

Fɔ mek dɛn no di pɔsin we dɛn de tink, dɛn fɔ tɛst di pikin in kromozom dɛn. Tu tɛst dɛn de fɔ dis:

1. Amniocentesis: dis involv fכ pas wan nidul we rili tכn tru yu bכdi, tek sכm sכm sכm sεmpl fכ di amniotic fluid we de rawnd di pikin, εn tεst di pikin in kromozom dεm na di sεl dεm.

2. Chorionic villus sampling (CVS): dis involv fכ tek wan sכm pat pan di plasεnta εn egzamin am.

Bikɔs i nɔ kin izi fɔ mek uman gɛt bɛlɛ wit dɛn tu tɛst ya, i impɔtant fɔ tɔk gud gud wan wit yu dɔktɔ bɔt di gud ɛn bad tin dɛn bifo yu disayd fɔ du sɔntin.

afta dεn bכn pikin, dεn kin kכnfכm dis bay we dεn tek sεmpl fכ di pikin in skin εn tεst di kromozom dεm.

Aw di tritmɛnt ɛn aw fɔ si am tan lɛk?

Bɔt i sɔri fɔ no se, no mɛrɛsin nɔ de fɔ mek pɔsin gɛt triplɔyd. I nɔ go ebul fɔ mɛn am. If dɛn bɔn pikin wit dis sik, di mɛdikal tim go jɔs gi sɔpɔt kia we dɛn de trit di pikin in sik dɛn.

bikɔs ɔf dis, bɔku pan di pikin dɛn we dɛn bɔn wit triplɔdi kin day insay sɔm dez ɔ mɔnt afta dɛn bɔn dɛn.

Bɔt, dɛn nɔ kin rili ripɔt bɔt pipul dɛn we dɔn liv te dɛn big. Dɛn gɛt wan spɛshal sik we dɛn kɔl mosaic triploidy . dis min se sכm sεl dεm na dεn bכdi gεt di nכmal 46 kromozom dεm, we כda wan dεm gεt כnli 69. bכt dεn kin gεt siriכs prכblεm dεm bak lεk fכ divεlכpmεnt delay, disabiliti fכ lan, εn sεiz.

Triploidy ɛn Trisomy na di sem tin?

Yɛs. Pan ɔl we dɛn tu nem ya kin tan lɛk di sem we we yu yɛri dɛn, dɛn tu nem ya na tu difrɛn tin dɛn.

  • triploidy na di adishכn fכ wan komplit εkstra sεt fכ kromozom dεm (23+23+23 = 69).
  • Trisomy na we yu ad jכs wan kromozom to wan nכmal pe kromozom. fכ egzampl, Down syndrome na wan kכndyushכn we dεn kכl ‘trisomy 21’. dis min se dεn ad εkstra kromozom to di 21st pe, we de mek di pe tri.

We ɛni mama ɔ papa lan bɔt dis kayn tin we kin mek i fil bad. So, i rili impɔtant fɔ gɛt di mɛrɛsin advays ɛn sɔpɔt we yu nid fɔ gɛt pan yu maynd.

Mɛsej we dɛn kin kɛr go na os

  • triploidy na di kromozom abnכmaliti we de apin randomly we uman de bכn. Nɔto ɛnibɔdi in fɔlt.
  • Dis sik kin dɔn bɔku tɛm we uman kin gɛt bɛlɛ we i bigin.
  • If yu gɛt ɛni ɔda tin we nɔ kɔmɔn we yu gɛt bɛlɛ (espɛshali di sayn dɛm we de sho se yu gɛt prɛ-ɛklampsia) , go to yu dɔktɔ wantɛm wantɛm.
  • No mɛrɛsin nɔ de fɔ dis sik, ɛn we dɛn dɔn bɔn pikin, na di kia nɔmɔ dɛn kin gi di pɔsin we gɛt di sik.
  • Saikɔlɔjik sɔpɔt rili impɔtant fɔ mama ɛn papa dɛm wae de go tru dis ɛkspiriɛns, so nɔr frayd fɔ tɔk bɔt am wit yu dɔktɔ, fambul, ɛn pipul dɛm wae yu lɛk.

Triploidy, bεlε, kromozom, miskεri, prεeklampsia, bכn difεkt, jεnεtik sik dεm

Frequently Asked Questions (FAQ)

Triploidy ɛn Trisomy na di sem tin?

Yɛs. Pan ɔl we dɛn tu nem ya kin tan lɛk di sem we we yu yɛri dɛn, dɛn tu nem ya na tu difrɛn tin dɛn.

⚠️ Important: The medical articles and information on Nirogi Lanka are for general awareness only, and are by no means a substitute for professional medical advice, diagnosis, or treatment. For any medical problem you have, consult a qualified physician immediately.

💬 Comments (0)

No kɔmɛnt nɔ de yet. Ad yu kɔmɛnt ya fɔ di fɔs tɛm.

Ad yu kɔmɛnt

Duya kɔlkul: 9 + 5 =