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An ka fɛn bɛɛ dɔn aw den ka NT scan (Nuchal Translucency Scan) kan kɔnɔbara la.

An ka fɛn bɛɛ dɔn aw den ka NT scan (Nuchal Translucency Scan) kan kɔnɔbara la.

Ni aw ye denba ye, a bɛ se ka kɛ aw ka dɔgɔtɔrɔ ye ‘NT scan’, walima ‘sɛgɛsɛgɛli min kɛra kɔnɔmaya saba fɔlɔ’ kan. Nin tɔgɔ in mɛnni bɛ se k’a to i bɛ siran dɔɔni ani ka ɲininkali kɛ. Nka tiɲɛ yɛrɛ la, o ye kɔrɔbɔli nɔgɔmanba ye, wa foyi tɛ yen min ka kan ka siran. Nin barokun in kɔnɔ, aw ka kan ka fɛn o fɛn dɔn nin NT sɛgɛsɛgɛli in kan, an bɛna kuma o bɛɛ kan.

NT scan ye mun ye tigitigi?

N’an y’a fɔ cogo nɔgɔman na, NT sɛgɛsɛgɛli ye ultrasound scan kɛrɛnkɛrɛnnen ye min bɛ kɛ i ka kɔnɔmaya kalo saba fɔlɔw la, dɔgɔkun 11 ni dɔgɔkun 14 cɛ.O tɔgɔ dafalen ye Nuchal Translucency scan ye. A bɛ a lajɛ kosɛbɛ farati min bɛ aw den na ni a bɛ se ka kɛ ni jamu bana dɔw ye, i n’a fɔ Down syndrome.

Tuma caman na, o sɛgɛsɛgɛli in bɛ kɛ ni joli sɛgɛsɛgɛli damadɔ wɛrɛw ye. Nin joli sɛgɛsɛgɛliw bɛ ɔrimɔni ni farikolojɔlifɛn dɔw hakɛ lajɛ aw joli la. I n'a fo:

O ɔrimɔni ni farikolojɔlifɛn ninnu bɛ musokɔnɔma bɛɛ farikolo la. Nka ni bana dɔ bɛ den na i n’a fɔ Down syndrome , u hakɛ bɛ se ka dɔgɔya walima ka caya ka tɛmɛ a cogo kɔrɔ kan. Ni NT sɛgɛsɛgɛli ni o joli sɛgɛsɛgɛliw kɛra ɲɔgɔn fɛ, an b’a wele ko ‘sɛgɛsɛgɛli faralen ɲɔgɔn kan kalo saba fɔlɔ kɔnɔ’ . O nɔw bɛ tiɲɛ ka tɛmɛ n’u kɛra ɲɔgɔn fɛ.

Nin sɛgɛsɛgɛli in bɛ mun de ɲini tigitigi?

Nin ye ko ye min ka di kosɛbɛ. Den o den bɛ falen kɔnɔbara la, fɛn finman dɔ bɛ a fari jukɔrɔ u kɔ kɔfɛ, a falen bɛ ji dɔɔni na. An b’o Weele ko ‘nuchal fold’. Nin ye fɛn ye den kɛnɛman bɛɛ bɛ min na.

Nka, den minnu ka jamu bana dɔw bɛ u la, ji caman bɛ lajɛ nin ‘nuchal fold’ in na ka tɛmɛ a cogo kɔrɔ kan. O kɔ, o membrane bɛ kɛ ka bonya dɔɔni. NT scan bɛ o janya suman.

Ka da o girinya kan, a bɛ se ka kɛ ka den ka jamu bana dɔ sɔrɔ farati la.

Condition (Sɔrɔcogo) Screened (Sɛgɛsɛgɛli).Ɲɛfɔli nɔgɔman
Down syndrome (Syndrome de down / Trisomie 21) . Cogo min na an ka seliluw bɛ ni kolosinsinnan 21 kopi wɛrɛ ye, walima kopi saba, sanni ka kɛ fila ye, an bɛ minnu sɔrɔ an ka selilu kɔnɔ cogoya la. O bɛ se ka nɔ bila hakili ni farikolo yiriwali la.
Trisomie 13 ani 18. Bamako, Mali O ni Down syndrome bɛ tali kɛ ɲɔgɔn na. Yan, kolosinsinnan 13 walima 18 kopi wɛrɛ bɛ yen.O ye banaw ye minnu bɛ bangekɔlɔsi fɛɛrɛw lase mɔgɔ ma minnu ka jugu kosɛbɛ.
Turner ka banakisɛfagalanw Bana min bɛ den musomanw dɔrɔn de minɛ minnu bɛ X kolosinsinnan ta. O cogo la, X kolosinsinnan yɔrɔ dɔ walima a bɛɛ tɛ yen. O bɛ se ka kɛ sababu ye ka yiriwali gɛlɛyaw ni dusukun gɛlɛyaw lase mɔgɔ ma.
Dusukunnabana min bɛ sɔrɔ bangekɔlɔsi fɛ Dusukunnabana dɔw bɛ yen bange waati. Dɔw bɛ se ka mɔgɔ ka ɲɛnamaya bila farati la, k’a sɔrɔ dɔw tɛ se ka gɛlɛya foyi lase mɔgɔ ma.

Nka a nafa ka bon ka aw hakili to nin na: NT scan ye sɛgɛsɛgɛli ye , a tɛ sɛgɛsɛgɛli ye min bɛ kɛ ka bana sɛgɛsɛgɛ . O kɔrɔ ye ko a tɛ a jira 100% ko nin bana ninnu bɛ den na. A b’a jira dɔrɔn ni o bana sugu sɔrɔli farati ka bon walima ni a ka dɔgɔn.

Ka fara nin kumaba in kan, dɔgɔtɔrɔ bɛna a janto fɛn damadɔ wɛrɛw la ni a bɛ nin sɛgɛsɛgɛli in kɛ.

  • Yala aw den bɛ ka bonya ka ɲɛ wa?
  • Den joli bɛ kɔnɔbara la?
  • Ni u ye filaninw ye, yala u bɛ denso kelen de ta wa?
  • aw bɛ aw jija ka kɔnɔmaya waati hakɛ dɔn tigitigi .

Mun bɛ kɛ NT sɛgɛsɛgɛli senfɛ?

Nin ye sɛgɛsɛgɛli ye min bɛ kɛ cogo la i n’a fɔ sɛgɛsɛgɛli wɛrɛw i ye minnu kɛ ka kɔrɔ. Foyi kɛrɛnkɛrɛnnen tɛ. A bɛna ɲini aw fɛ aw ka jifilen 2 fo 3 min lɛri kelen ɲɔgɔn sani aw ka sɛgɛsɛgɛli kɛ. O kun ye ko a ka nɔgɔn ka den ye ka ɲɛ ni aw ka sugunɛ falen don. O la, aw kana koli kɛ sani aw ka sɛgɛsɛgɛli kɛ. Hali ni a bɛ se ka kɛ ko a tɛ diya dɔɔni, o bɛna a dɛmɛ ka sɛgɛsɛgɛli kɛ ka ɲɛ.

Ni aw donna sɛgɛsɛgɛlikɛyɔrɔ la, a bɛna ɲini aw fɛ aw ka aw da dilan kan. O kɔfɛ, fɛɛrɛtigi bɛna jeli dɔɔni kɛ aw kɔnɔbara dugumayanfan na ka minɛn fitinin dɔ (bere/sonda) tɛmɛ a fɛ walasa ka ja ta. Aw bɛna degun dɔɔni ye nin waati in na, nka a tɛna kɛ dimi ye . Ni ja wajibiyalenw tara ka ban, sɛgɛsɛgɛli bɛ ban. Aw bɛ se ka taa so i n’a fɔ a bɛ kɛ cogo min na.

Yala a ka kan ka nin sɛgɛsɛgɛli in kɛ wa?

Ayi, NT sɛgɛsɛgɛli tɛ sɛgɛsɛgɛli wajibiyalen ye. A ye ŋaniyataama ye pewu. O kɔrɔ ye ko jo dafalen b’i bolo k’a latigɛ ni i bɛna a sɔrɔ walima ni i tɛna a sɔrɔ.

A ka di bangebaga dɔw ye ka nin sɛgɛsɛgɛli in kɛ ani ka kɔn ka u den ka kɛnɛyako gɛlɛyaw dɔn. O cogo la, ni den dɔ bɛ yen mago kɛrɛnkɛrɛnnen bɛ min na, u bɛ waati sɔrɔ k’u labɛn hakili ta fan fɛ ani cogo wɛrɛ bɛɛ la walasa k’o den ladon.

Ani fana, bangebaga dɔw b’a miiri ko o sɛgɛsɛgɛli sugu bɛ se ka degun kunntanw lase mɔgɔ ma. U bɛ se k’a latigɛ ko u tɛna sɛgɛsɛgɛli kɛ ni o jaabiw ma fɛn caman Changé u ka den ladoncogo la. O desizɔn fila bɛɛ ye tiɲɛ ye. Min nafa ka bon, o ye ko aw ni aw jɛɲɔgɔn ka desizɔn ta min ka fisa aw ma, aw ni aw ka dɔgɔtɔrɔ faralen ɲɔgɔn kan ni a mago bɛ a la.

Scan jaabiw faamuya cogo di?

Ni den bɛ ka bonya kɔnɔbara la, an ye kuma min fɔ ka tɛmɛ nuchal fold min kan, o fana bɛ bonya dɔɔni dɔɔni. O la, sumanikɛlan min bɛ sɔrɔ sɛgɛsɛgɛli kɛtuma na, o bɛ suma ni den kɛnɛman tɔw ka sumanikɛlan cɛmancɛ ye minnu si hakɛ ye kelen ye.

Jaabi Cogojirali
O kɔlɔlɔ cɛmancɛ (Rasque dɔgɔman) . A bɛ jate ko a bɛnnen don ni sumanikɛlan ka se milimɛtɛrɛ 2 ma dɔgɔkun 11 kɔnɔ ani ka se milimɛtɛrɛ 2,8 ma dɔgɔkun 13 ni tile 6 kɔnɔ. O kɔrɔ ye ko den ka farati ka dɔgɔn ka kɛ sababu ye ka bana dɔ sɔrɔ min bɛ bɔ a la.
Résultat abnormal (Faraba) . Ni sumanikɛlan bɛ tɛmɛ hakɛ danmadɔ kan min kofɔlen don sanfɛ, o bɛ jate "faratiba" nɔ ye. O kɔrɔ tɛ ko bana dɔ bɛ den na, nka a bɛ kɛ dɔrɔn ko a farati ka bon ka tɛmɛ a cogo kɔrɔ kan.

Aw ka dɔgɔtɔrɔ tɛna baara kɛ ni nin sɛgɛsɛgɛli sumanikɛlan in dɔrɔn ye, nka a tɛna aw si hakɛ ni aw joli sɛgɛsɛgɛli jaabiw fana kɛ walasa ka bana sɛgɛsɛgɛli laban kɛ. Ni u farala ɲɔgɔn kan, NT sɛgɛsɛgɛli ni joli sɛgɛsɛgɛli bɛ se ka farati fɔ jamu cogoyaw la ni 85% ɲɔgɔn ye .

Nka, "false positive" sɔrɔli bɛ se ka kɛ 5% ye. O kɔrɔ ye ko den bɛ se ka kɛ faratiba ye, hali ni gɛlɛya foyi tɛ a la.

Ni NT scan jaabiw ma kɛ cogo la, aw ka kan ka mun kɛ?

Fɔlɔ, i kana siran . Ni ‘faratiba’ kɔlɔlɔ tɛ a la, o kɔrɔ tɛ ko gɛlɛya bɛ den na. O kɔrɔ dɔrɔn ye ko sɛgɛsɛgɛli wɛrɛw ka kan ka kɛ.

Aw ka dɔgɔtɔrɔ bɛna sɛgɛsɛgɛli wɛrɛw fɔ aw ye minnu bɛ se ka kɛ. Nin sɛgɛsɛgɛli ninnu bɛ se ka kɛ sababu ye ka bana sɛgɛsɛgɛli kɛ ka ɲɛ 100%.

  • Chorionic Villus Sampling (CVS): Nin yɔrɔ in na, farikolo yɔrɔ fitinin dɔ bɛ bɔ denso kɔnɔ ka a lajɛ.
  • Amniocentesis : O ye ka denso kɔnɔji dɔ ta ka a sɛgɛsɛgɛ.
  • ADN min tɛ bangekɔlɔsi kɔnɔ (cfDNA) sɛgɛsɛgɛli : Nin ye joli sɛgɛsɛgɛli nɔgɔman ye min bɛ den ka ADN yɔrɔ dɔw sɛgɛsɛgɛ aw joli la walasa ka jamu cogoyaw sɛgɛsɛgɛ. ( Nin ye joli sɛgɛsɛgɛli nɔgɔman ye min bɛ i den ka ADN yɔrɔ dɔw sɛgɛsɛgɛ i joli la walasa ka jamu cogoyaw sɛgɛsɛgɛ).

Aw ka dɔgɔtɔrɔ bɛna o sɛgɛsɛgɛli kelen-kelen bɛɛ nafa, a dɛsɛ ani a faratiw ɲɛfɔ aw ye, ka kɛɲɛ ni aw ka ko ye. O kɔ, aw bɛ se k’a latigɛ ni aw bɛna u sɔrɔ walima ni aw tɛna u sɔrɔ.

Take-Home cikan

  • NT scan ye ultrasound sɛgɛsɛgɛli ye min tɛ mɔgɔ tɔɔrɔ pewu, wa dimi tɛ a la, min bɛ kɛ kɔnɔmaya kɔnɔmaya kalo saba fɔlɔ kɔnɔ.
  • Wajibi tɛ ka o kɛ. O bɛɛ bɛ i yɛrɛ de bolo.
  • O bɛ sɛgɛsɛgɛli kɛ jamu banaw farati la i n’a fɔ Down syndrome, nka a tɛ bana in sɔrɔli dafa.
  • Ni aw ye ‘faratiba’ jaabi sɔrɔ, aw kana siran, nka aw bɛ kuma aw ka dɔgɔtɔrɔ fɛ walasa ka sɛgɛsɛgɛli wɛrɛw kɛ.
  • Aw kana sigasiga abada ka baro kɛ aw ka gɛlɛyaw ni aw ka sigasigaw bɛɛ kan ani ka u ɲɛfɔ aw ka dɔgɔtɔrɔ ye.

NT Scan, Nuchal Translucency Scan, Kɔnɔmaya, Down Syndrome, Down syndrome, Genetic Diseases, Sɛgɛsɛgɛli kalo saba fɔlɔ, Denw ka Scan
⚠️ 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)

Ko foyi ma bila fɔlɔ. Aw ka kuma fɔlen fara a kan yan a siɲɛ fɔlɔ la.

Aw ka kuma fɔlen fara a kan

Aw ye jatebɔ kɛ: 2 + 4 =
An ka fɛn bɛɛ dɔn aw den ka NT scan (Nuchal Translucency Scan) kan kɔnɔbara la.

An ka fɛn bɛɛ dɔn aw den ka NT scan (Nuchal Translucency Scan) kan kɔnɔbara la.

Ni aw ye denba ye, a bɛ se ka kɛ aw ka dɔgɔtɔrɔ ye ‘NT scan’, walima ‘sɛgɛsɛgɛli min kɛra kɔnɔmaya saba fɔlɔ’ kan. Nin tɔgɔ in mɛnni bɛ se k’a to i bɛ siran dɔɔni ani ka ɲininkali kɛ. Nka tiɲɛ yɛrɛ la, o ye kɔrɔbɔli nɔgɔmanba ye, wa foyi tɛ yen min ka kan ka siran. Nin barokun in kɔnɔ, aw ka kan ka fɛn o fɛn dɔn nin NT sɛgɛsɛgɛli in kan, an bɛna kuma o bɛɛ kan.

NT scan ye mun ye tigitigi?

N’an y’a fɔ cogo nɔgɔman na, NT sɛgɛsɛgɛli ye ultrasound scan kɛrɛnkɛrɛnnen ye min bɛ kɛ i ka kɔnɔmaya kalo saba fɔlɔw la, dɔgɔkun 11 ni dɔgɔkun 14 cɛ.O tɔgɔ dafalen ye Nuchal Translucency scan ye. A bɛ a lajɛ kosɛbɛ farati min bɛ aw den na ni a bɛ se ka kɛ ni jamu bana dɔw ye, i n’a fɔ Down syndrome.

Tuma caman na, o sɛgɛsɛgɛli in bɛ kɛ ni joli sɛgɛsɛgɛli damadɔ wɛrɛw ye. Nin joli sɛgɛsɛgɛliw bɛ ɔrimɔni ni farikolojɔlifɛn dɔw hakɛ lajɛ aw joli la. I n'a fo:

O ɔrimɔni ni farikolojɔlifɛn ninnu bɛ musokɔnɔma bɛɛ farikolo la. Nka ni bana dɔ bɛ den na i n’a fɔ Down syndrome , u hakɛ bɛ se ka dɔgɔya walima ka caya ka tɛmɛ a cogo kɔrɔ kan. Ni NT sɛgɛsɛgɛli ni o joli sɛgɛsɛgɛliw kɛra ɲɔgɔn fɛ, an b’a wele ko ‘sɛgɛsɛgɛli faralen ɲɔgɔn kan kalo saba fɔlɔ kɔnɔ’ . O nɔw bɛ tiɲɛ ka tɛmɛ n’u kɛra ɲɔgɔn fɛ.

Nin sɛgɛsɛgɛli in bɛ mun de ɲini tigitigi?

Nin ye ko ye min ka di kosɛbɛ. Den o den bɛ falen kɔnɔbara la, fɛn finman dɔ bɛ a fari jukɔrɔ u kɔ kɔfɛ, a falen bɛ ji dɔɔni na. An b’o Weele ko ‘nuchal fold’. Nin ye fɛn ye den kɛnɛman bɛɛ bɛ min na.

Nka, den minnu ka jamu bana dɔw bɛ u la, ji caman bɛ lajɛ nin ‘nuchal fold’ in na ka tɛmɛ a cogo kɔrɔ kan. O kɔ, o membrane bɛ kɛ ka bonya dɔɔni. NT scan bɛ o janya suman.

Ka da o girinya kan, a bɛ se ka kɛ ka den ka jamu bana dɔ sɔrɔ farati la.

Condition (Sɔrɔcogo) Screened (Sɛgɛsɛgɛli).Ɲɛfɔli nɔgɔman
Down syndrome (Syndrome de down / Trisomie 21) . Cogo min na an ka seliluw bɛ ni kolosinsinnan 21 kopi wɛrɛ ye, walima kopi saba, sanni ka kɛ fila ye, an bɛ minnu sɔrɔ an ka selilu kɔnɔ cogoya la. O bɛ se ka nɔ bila hakili ni farikolo yiriwali la.
Trisomie 13 ani 18. Bamako, Mali O ni Down syndrome bɛ tali kɛ ɲɔgɔn na. Yan, kolosinsinnan 13 walima 18 kopi wɛrɛ bɛ yen.O ye banaw ye minnu bɛ bangekɔlɔsi fɛɛrɛw lase mɔgɔ ma minnu ka jugu kosɛbɛ.
Turner ka banakisɛfagalanw Bana min bɛ den musomanw dɔrɔn de minɛ minnu bɛ X kolosinsinnan ta. O cogo la, X kolosinsinnan yɔrɔ dɔ walima a bɛɛ tɛ yen. O bɛ se ka kɛ sababu ye ka yiriwali gɛlɛyaw ni dusukun gɛlɛyaw lase mɔgɔ ma.
Dusukunnabana min bɛ sɔrɔ bangekɔlɔsi fɛ Dusukunnabana dɔw bɛ yen bange waati. Dɔw bɛ se ka mɔgɔ ka ɲɛnamaya bila farati la, k’a sɔrɔ dɔw tɛ se ka gɛlɛya foyi lase mɔgɔ ma.

Nka a nafa ka bon ka aw hakili to nin na: NT scan ye sɛgɛsɛgɛli ye , a tɛ sɛgɛsɛgɛli ye min bɛ kɛ ka bana sɛgɛsɛgɛ . O kɔrɔ ye ko a tɛ a jira 100% ko nin bana ninnu bɛ den na. A b’a jira dɔrɔn ni o bana sugu sɔrɔli farati ka bon walima ni a ka dɔgɔn.

Ka fara nin kumaba in kan, dɔgɔtɔrɔ bɛna a janto fɛn damadɔ wɛrɛw la ni a bɛ nin sɛgɛsɛgɛli in kɛ.

  • Yala aw den bɛ ka bonya ka ɲɛ wa?
  • Den joli bɛ kɔnɔbara la?
  • Ni u ye filaninw ye, yala u bɛ denso kelen de ta wa?
  • aw bɛ aw jija ka kɔnɔmaya waati hakɛ dɔn tigitigi .

Mun bɛ kɛ NT sɛgɛsɛgɛli senfɛ?

Nin ye sɛgɛsɛgɛli ye min bɛ kɛ cogo la i n’a fɔ sɛgɛsɛgɛli wɛrɛw i ye minnu kɛ ka kɔrɔ. Foyi kɛrɛnkɛrɛnnen tɛ. A bɛna ɲini aw fɛ aw ka jifilen 2 fo 3 min lɛri kelen ɲɔgɔn sani aw ka sɛgɛsɛgɛli kɛ. O kun ye ko a ka nɔgɔn ka den ye ka ɲɛ ni aw ka sugunɛ falen don. O la, aw kana koli kɛ sani aw ka sɛgɛsɛgɛli kɛ. Hali ni a bɛ se ka kɛ ko a tɛ diya dɔɔni, o bɛna a dɛmɛ ka sɛgɛsɛgɛli kɛ ka ɲɛ.

Ni aw donna sɛgɛsɛgɛlikɛyɔrɔ la, a bɛna ɲini aw fɛ aw ka aw da dilan kan. O kɔfɛ, fɛɛrɛtigi bɛna jeli dɔɔni kɛ aw kɔnɔbara dugumayanfan na ka minɛn fitinin dɔ (bere/sonda) tɛmɛ a fɛ walasa ka ja ta. Aw bɛna degun dɔɔni ye nin waati in na, nka a tɛna kɛ dimi ye . Ni ja wajibiyalenw tara ka ban, sɛgɛsɛgɛli bɛ ban. Aw bɛ se ka taa so i n’a fɔ a bɛ kɛ cogo min na.

Yala a ka kan ka nin sɛgɛsɛgɛli in kɛ wa?

Ayi, NT sɛgɛsɛgɛli tɛ sɛgɛsɛgɛli wajibiyalen ye. A ye ŋaniyataama ye pewu. O kɔrɔ ye ko jo dafalen b’i bolo k’a latigɛ ni i bɛna a sɔrɔ walima ni i tɛna a sɔrɔ.

A ka di bangebaga dɔw ye ka nin sɛgɛsɛgɛli in kɛ ani ka kɔn ka u den ka kɛnɛyako gɛlɛyaw dɔn. O cogo la, ni den dɔ bɛ yen mago kɛrɛnkɛrɛnnen bɛ min na, u bɛ waati sɔrɔ k’u labɛn hakili ta fan fɛ ani cogo wɛrɛ bɛɛ la walasa k’o den ladon.

Ani fana, bangebaga dɔw b’a miiri ko o sɛgɛsɛgɛli sugu bɛ se ka degun kunntanw lase mɔgɔ ma. U bɛ se k’a latigɛ ko u tɛna sɛgɛsɛgɛli kɛ ni o jaabiw ma fɛn caman Changé u ka den ladoncogo la. O desizɔn fila bɛɛ ye tiɲɛ ye. Min nafa ka bon, o ye ko aw ni aw jɛɲɔgɔn ka desizɔn ta min ka fisa aw ma, aw ni aw ka dɔgɔtɔrɔ faralen ɲɔgɔn kan ni a mago bɛ a la.

Scan jaabiw faamuya cogo di?

Ni den bɛ ka bonya kɔnɔbara la, an ye kuma min fɔ ka tɛmɛ nuchal fold min kan, o fana bɛ bonya dɔɔni dɔɔni. O la, sumanikɛlan min bɛ sɔrɔ sɛgɛsɛgɛli kɛtuma na, o bɛ suma ni den kɛnɛman tɔw ka sumanikɛlan cɛmancɛ ye minnu si hakɛ ye kelen ye.

Jaabi Cogojirali
O kɔlɔlɔ cɛmancɛ (Rasque dɔgɔman) . A bɛ jate ko a bɛnnen don ni sumanikɛlan ka se milimɛtɛrɛ 2 ma dɔgɔkun 11 kɔnɔ ani ka se milimɛtɛrɛ 2,8 ma dɔgɔkun 13 ni tile 6 kɔnɔ. O kɔrɔ ye ko den ka farati ka dɔgɔn ka kɛ sababu ye ka bana dɔ sɔrɔ min bɛ bɔ a la.
Résultat abnormal (Faraba) . Ni sumanikɛlan bɛ tɛmɛ hakɛ danmadɔ kan min kofɔlen don sanfɛ, o bɛ jate "faratiba" nɔ ye. O kɔrɔ tɛ ko bana dɔ bɛ den na, nka a bɛ kɛ dɔrɔn ko a farati ka bon ka tɛmɛ a cogo kɔrɔ kan.

Aw ka dɔgɔtɔrɔ tɛna baara kɛ ni nin sɛgɛsɛgɛli sumanikɛlan in dɔrɔn ye, nka a tɛna aw si hakɛ ni aw joli sɛgɛsɛgɛli jaabiw fana kɛ walasa ka bana sɛgɛsɛgɛli laban kɛ. Ni u farala ɲɔgɔn kan, NT sɛgɛsɛgɛli ni joli sɛgɛsɛgɛli bɛ se ka farati fɔ jamu cogoyaw la ni 85% ɲɔgɔn ye .

Nka, "false positive" sɔrɔli bɛ se ka kɛ 5% ye. O kɔrɔ ye ko den bɛ se ka kɛ faratiba ye, hali ni gɛlɛya foyi tɛ a la.

Ni NT scan jaabiw ma kɛ cogo la, aw ka kan ka mun kɛ?

Fɔlɔ, i kana siran . Ni ‘faratiba’ kɔlɔlɔ tɛ a la, o kɔrɔ tɛ ko gɛlɛya bɛ den na. O kɔrɔ dɔrɔn ye ko sɛgɛsɛgɛli wɛrɛw ka kan ka kɛ.

Aw ka dɔgɔtɔrɔ bɛna sɛgɛsɛgɛli wɛrɛw fɔ aw ye minnu bɛ se ka kɛ. Nin sɛgɛsɛgɛli ninnu bɛ se ka kɛ sababu ye ka bana sɛgɛsɛgɛli kɛ ka ɲɛ 100%.

  • Chorionic Villus Sampling (CVS): Nin yɔrɔ in na, farikolo yɔrɔ fitinin dɔ bɛ bɔ denso kɔnɔ ka a lajɛ.
  • Amniocentesis : O ye ka denso kɔnɔji dɔ ta ka a sɛgɛsɛgɛ.
  • ADN min tɛ bangekɔlɔsi kɔnɔ (cfDNA) sɛgɛsɛgɛli : Nin ye joli sɛgɛsɛgɛli nɔgɔman ye min bɛ den ka ADN yɔrɔ dɔw sɛgɛsɛgɛ aw joli la walasa ka jamu cogoyaw sɛgɛsɛgɛ. ( Nin ye joli sɛgɛsɛgɛli nɔgɔman ye min bɛ i den ka ADN yɔrɔ dɔw sɛgɛsɛgɛ i joli la walasa ka jamu cogoyaw sɛgɛsɛgɛ).

Aw ka dɔgɔtɔrɔ bɛna o sɛgɛsɛgɛli kelen-kelen bɛɛ nafa, a dɛsɛ ani a faratiw ɲɛfɔ aw ye, ka kɛɲɛ ni aw ka ko ye. O kɔ, aw bɛ se k’a latigɛ ni aw bɛna u sɔrɔ walima ni aw tɛna u sɔrɔ.

Take-Home cikan

  • NT scan ye ultrasound sɛgɛsɛgɛli ye min tɛ mɔgɔ tɔɔrɔ pewu, wa dimi tɛ a la, min bɛ kɛ kɔnɔmaya kɔnɔmaya kalo saba fɔlɔ kɔnɔ.
  • Wajibi tɛ ka o kɛ. O bɛɛ bɛ i yɛrɛ de bolo.
  • O bɛ sɛgɛsɛgɛli kɛ jamu banaw farati la i n’a fɔ Down syndrome, nka a tɛ bana in sɔrɔli dafa.
  • Ni aw ye ‘faratiba’ jaabi sɔrɔ, aw kana siran, nka aw bɛ kuma aw ka dɔgɔtɔrɔ fɛ walasa ka sɛgɛsɛgɛli wɛrɛw kɛ.
  • Aw kana sigasiga abada ka baro kɛ aw ka gɛlɛyaw ni aw ka sigasigaw bɛɛ kan ani ka u ɲɛfɔ aw ka dɔgɔtɔrɔ ye.

NT Scan, Nuchal Translucency Scan, Kɔnɔmaya, Down Syndrome, Down syndrome, Genetic Diseases, Sɛgɛsɛgɛli kalo saba fɔlɔ, Denw ka Scan
⚠️ 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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