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Triple X Syndrome ye mun ye? An ka kuma nin bana in kan min man teli ka sɔrɔ

Triple X Syndrome ye mun ye? An ka kuma nin bana in kan min man teli ka sɔrɔ

Fɛn dɔ bɛ an bɛɛ la min bɛ wele ko ‘chromosomes’ an farikolo yɔrɔw kɔnɔ. Aw k’a miiri k’u ye an farikolo bolodalenw ye. Fɛn bɛɛ, k’a ta an janya la ka taa a bila an ɲɛ kulɛri la ka taa a bila an kunsigi cogoya la, o bɛɛ bɛ dɔn ni o kolosinsinnanw ka jɛnɛya ye. A ka c’a la, muso bɛ ni ‘X’ kolosinsinnan fila ye, cɛ dɔ bɛ ni ‘X’ kelen ye ani ‘Y’ kelen. Nka a man teli kosɛbɛ, npogotiginin dɔw bɛ bange ni ‘X’ kolosinsinnan wɛrɛ ye. O ye jamu bana ye an bɛ min wele ko Triple X Syndrome, walima 47,XXX. Aw kana siran ni aw ye nin mɛn, a ka ca a la a tɛ kojugu ye. An ka kuma o kan ka ɲɛ.

Mun na o bɛ ka kɛ? O kun ye mun ye?

N’an y’a fɔ cogo nɔgɔman na, triple X syndrome ye ko ye min bɛ kɛ k’a sɔrɔ a ma kɛ cogo si la pewu . A tɛ sɔrɔ mɔgɔ si ka hakɛ la. X kolosinsinnan wɛrɛ bɛ fara a kan ka da fili fitinin dɔ kan ba kɔnɔbara walima fa ka cɛya selilɛri tilali la ni den kɔnɔma don. Walima a bɛ se ka kɛ selilu tilali waati la denso yiriwali daminɛ na.

Min nafa ka bon, o ye ko nin tɛ fɛn ye min bɛ se ka bali. Ani fana, hali ni nin bana in bɛ denba la, a ka ca a la a bɛ se ka a lase a denw ma, o ka dɔgɔn kosɛbɛ.

Hali ni a jirala ko nin bana in farati ka bon dɔɔni npogotigininw na minnu bangera denba minnu si tɛmɛna san 35 kan, a jatera ko a man teli ka kɛ denba minnu si hakɛ bɛ se ka kɛ denbaw la minnu si bɛ san suguya bɛɛ la.

Tuma dɔw la, o X kolosinsinnan wɛrɛ tɛ sɔrɔ farikolo yɔrɔw bɛɛ la. A bɛ sɔrɔ seli dɔw dɔrɔn de la. O kɔrɔ ye ko seli dɔw bɛ kɛ cogoya la (XX), ka sɔrɔ selilu dɔw bɛ (XXX). Furakɛcogo la, an b’o wele ko ‘mozayika’ bana.

Nin bana in taamasiɲɛw ye jumɛnw ye?

O yɔrɔ de la mɔgɔ caman bɛ kabakoya. A ka ca a la, npogotigininw ni musow minnu bɛ ni triple X syndrome ye, taamasiɲɛ jɛlen tɛ olu la , walima taamasiɲɛ nɔgɔmanw dɔrɔn de bɛ u la . O de kama a bɛ fɔ ko bana in bɛ mɔgɔ tan o tan na, kelen dɔrɔn de bɛ sɔrɔ. Mɔgɔ caman bɛ ɲɛnamaya kɛ cogo bɛnnen na, kɛnɛya la, k’a sɔrɔ u yɛrɛ t’a dɔn ko bana in bɛ u la.

Nka, mɔgɔ dɔw bɛ se ka taamasiɲɛ dɔw sɔrɔ. Nin taamasiɲɛ ninnu bɛ se ka ɲɔgɔn ta mɔgɔ kelen-kelen bɛɛ la. An k’o taamasiɲɛw tila-tila kuluw ye.

Jogo suguya Fɛn minnu ka kan ka ye
Farikolo Taamaʃyɛnw

  • Ka janya ka tɛmɛ mɔgɔ hakɛ danma kan (kɛrɛnkɛrɛnnenya la ni sen janw) .
  • Ɲɛw ni ɲɔgɔn cɛ janya bɛ bonya dɔɔni
  • Ɲɛ kɔnɔna bɛ datugu ni fari ye (Epicanthal folds) .
  • Senw fla ye
  • Tuma dɔw la, bolokɔnincinin bɛ kɔrɔta dɔɔni.
  • Yɛlɛma misɛnniw bɛ kɛ barajuru cogoya la
  • A man teli, kirinni
  • Gɛlɛya minnu bɛ sɔrɔ sugunɛ walima kɔnɔbara la
  • Dusukun tantanni misɛnniw

Jogo minnu bɛ tali kɛ bonya, kalan ani hakili kɛnɛya la

  • Kuma ni kanko latɛmɛni
  • Kalanbaliya walima IQ ka dɔgɔn dɔɔni ka tɛmɛ balimakɛw kan
  • Jateminɛ-dɛsɛbana
  • Sosiyete ka sekow ni gɛlɛyaw ka ɲɛsin mɔgɔ wɛrɛw ma
  • Dɔ farala a ka teli ka bana dɔw sɔrɔ i n’a fɔ jɔrɔnanko ni degun
  • Yɛrɛbonya dɔgɔyali

K’a sɔrɔ nin taamasiɲɛ kelen walima caman bɛ aw den na, o kɔrɔ tɛ ko triple X syndrome bɛ a la. U bɛ se ka sɔrɔ fɛn caman wɛrɛw fɛ, o la ni haminanko dɔw bɛ aw la, a ka fisa aw ka kuma dɔgɔtɔrɔ dɔ fɛ.

Aw bɛ nin bana in dɔn cogo di?

Tuma caman na, o bana in bɛ sɔrɔ a danma. Misali la, a bɛ se ka sɔrɔ ni muso bɛ fura ɲini gɛlɛya dɔ la i n’a fɔ bange gɛlɛya walima kalolabɔ joona.

Fɛɛrɛ wɛrɛw ye:

  • Sɛgɛsɛgɛli minnu bɛ kɛ kɔnɔmaya waati : Jɛnɛya sɛgɛsɛgɛli i n’a fɔ NIPT (Non-Invasive Prenatal Testing) , Amniocentesis , walima CVS (Chorionic Villus Sampling) minnu bɛ kɛ denba kɔnɔma kan, olu bɛ se ka nin bana in dɔn sani den ka bange.
  • Joli sɛgɛsɛgɛliw : Den bangenen kɔfɛ, ni dɔgɔtɔrɔ bɛ sigasiga, kariyotipi sɛgɛsɛgɛli bɛ se ka kɛ walasa ka o dafa. Nin sɛgɛsɛgɛli in bɛ se k’a dɔn ni X kolosinsinnan wɛrɛ bɛ yen ani ni a bɛ farikolokisɛ kɛmɛsarada la joli la.

O furakɛcogo jumɛnw bɛ yen?

Fɛn fɔlɔ min ka kan ka to an hakili la, o ye ko jamu bana min bɛ wele ko Triple X Syndrome , o tɛ se ka kɛnɛya pewu.Sabula o ye fɛn ye min bɛ na ni an ka jeninida ye. Nka, ni a bɛ se ka gɛlɛyaw ni taamasiɲɛ minnu lase i ma, ni olu dɛmɛna ani k’u ɲɛnabɔ, i bɛ se ka ɲɛnamaya kɛ cogo la min bɛ bɛn pewu, ani ka ɲɛnamaya kɛ nisɔndiya la .

Furakɛli bɛ latigɛ ka kɛɲɛ ni mɔgɔ kelen-kelen bɛɛ ka bana taamasiɲɛw ni a magow ye.

  • Dɔgɔtɔrɔso lajɛw kɛli tuma bɛɛ: Dɔgɔtɔrɔ bɛ se ka sɛgɛsɛgɛliw kɛ i n’a fɔ ultrasound scan ani echocardiogramme (EKG) walasa ka gɛlɛya o gɛlɛya sɔrɔ sugunɛ, kɔnɔbara ani dusukun na.
  • Dɛmɛ baaradaw ni furakɛlicogo: Nin ye yɔrɔ ye min nafa ka bon kosɛbɛ.
  • Kuma ni kan furakɛli : O nafa ka bon kosɛbɛ denmisɛn minnu ka kuma bɛ mɛn.
  • Farikoloɲɛnajɛ furakɛcogo : A bɛ se ka dɛmɛ don ni farikolo fanga dɔgɔyara walima ni balansi gɛlɛyaw bɛ aw la.
  • Kalan dɛmɛni: Kalan gɛlɛya bɛ denmisɛn minnu na, olu bɛ se ka dɛmɛ kɛrɛnkɛrɛnnen sɔrɔ lakɔliso la.
  • Ladilikan: Ladilikan nafa ka bon kosɛbɛ jɔrɔnanko, degun, walima gɛlɛyaw ɲɛnabɔli la sigidamɔgɔw ni ɲɔgɔn cɛ jɛɲɔgɔnyaw la.
  • Ɔrimɔni furakɛli : Tuma dɔw la, dɔgɔtɔrɔ bɛ se ka fɛnw fɔ i n’a fɔ ɔrimɔni furakɛli walasa ka gɛlɛyaw furakɛ minnu bɛ sɔrɔ kɔnɔbara baara dɔgɔyali fɛ walima ka den janya kunbɛn.

Min nafa ka bon kosɛbɛ, o ye ka bana in dɔn joona ani ka dɛmɛ ni furakɛli wajibiyalenw kɛ walasa den ka se ka se a seko bɛɛ la.

Take-Home cikan

  • Triple X syndrome ye bana ye min bɛ sɔrɔ jamu fɛ, a bɛ npogotigininw dɔrɔn de minɛ, wa a bɛ kɛ k’a sɔrɔ a ma kɛ cogo si la. O tɛ mɔgɔ si ka jalaki ye.
  • Nin bana in bɛ musow ni npogotigi caman na, taamasiɲɛ foyi tɛ u la, wa u bɛ ɲɛnamaya kɛ cogo la min bɛ kɛnɛya pewu, min bɛ kɛ cogo la.
  • Hali ni fura kɛrɛnkɛrɛnnen tɛ o la, taamasiɲɛ o taamasiɲɛ bɛ sɔrɔ (kuma gɛlɛya, kalan gɛlɛya, hakili gɛlɛya) bɛ se ka ɲɛnabɔ ka ɲɛ ni furakɛli ni dɛmɛ ye.
  • Ni haminanko walima ɲininkali dɔw bɛ aw den ka yiriwali, a kɛcogo, walima a ka kalan kan, aw kana siran ka kuma aw ka dɔgɔtɔrɔ fɛ. K’a dɔn joona ani ka dɛmɛ don, o de ye fɛn ɲumanw ye minnu bɛ se ka kɛ.

Triple X Syndrome, 47,XXX, bana minnu bɛ sɔrɔ jamu fɛ, kolosinsinnanw, npogotigininw ka kɛnɛya, yiriwali gɛlɛyaw, kalanbaliya
⚠️ 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: 7 + 1 =
Triple X Syndrome ye mun ye? An ka kuma nin bana in kan min man teli ka sɔrɔ

Triple X Syndrome ye mun ye? An ka kuma nin bana in kan min man teli ka sɔrɔ

Fɛn dɔ bɛ an bɛɛ la min bɛ wele ko ‘chromosomes’ an farikolo yɔrɔw kɔnɔ. Aw k’a miiri k’u ye an farikolo bolodalenw ye. Fɛn bɛɛ, k’a ta an janya la ka taa a bila an ɲɛ kulɛri la ka taa a bila an kunsigi cogoya la, o bɛɛ bɛ dɔn ni o kolosinsinnanw ka jɛnɛya ye. A ka c’a la, muso bɛ ni ‘X’ kolosinsinnan fila ye, cɛ dɔ bɛ ni ‘X’ kelen ye ani ‘Y’ kelen. Nka a man teli kosɛbɛ, npogotiginin dɔw bɛ bange ni ‘X’ kolosinsinnan wɛrɛ ye. O ye jamu bana ye an bɛ min wele ko Triple X Syndrome, walima 47,XXX. Aw kana siran ni aw ye nin mɛn, a ka ca a la a tɛ kojugu ye. An ka kuma o kan ka ɲɛ.

Mun na o bɛ ka kɛ? O kun ye mun ye?

N’an y’a fɔ cogo nɔgɔman na, triple X syndrome ye ko ye min bɛ kɛ k’a sɔrɔ a ma kɛ cogo si la pewu . A tɛ sɔrɔ mɔgɔ si ka hakɛ la. X kolosinsinnan wɛrɛ bɛ fara a kan ka da fili fitinin dɔ kan ba kɔnɔbara walima fa ka cɛya selilɛri tilali la ni den kɔnɔma don. Walima a bɛ se ka kɛ selilu tilali waati la denso yiriwali daminɛ na.

Min nafa ka bon, o ye ko nin tɛ fɛn ye min bɛ se ka bali. Ani fana, hali ni nin bana in bɛ denba la, a ka ca a la a bɛ se ka a lase a denw ma, o ka dɔgɔn kosɛbɛ.

Hali ni a jirala ko nin bana in farati ka bon dɔɔni npogotigininw na minnu bangera denba minnu si tɛmɛna san 35 kan, a jatera ko a man teli ka kɛ denba minnu si hakɛ bɛ se ka kɛ denbaw la minnu si bɛ san suguya bɛɛ la.

Tuma dɔw la, o X kolosinsinnan wɛrɛ tɛ sɔrɔ farikolo yɔrɔw bɛɛ la. A bɛ sɔrɔ seli dɔw dɔrɔn de la. O kɔrɔ ye ko seli dɔw bɛ kɛ cogoya la (XX), ka sɔrɔ selilu dɔw bɛ (XXX). Furakɛcogo la, an b’o wele ko ‘mozayika’ bana.

Nin bana in taamasiɲɛw ye jumɛnw ye?

O yɔrɔ de la mɔgɔ caman bɛ kabakoya. A ka ca a la, npogotigininw ni musow minnu bɛ ni triple X syndrome ye, taamasiɲɛ jɛlen tɛ olu la , walima taamasiɲɛ nɔgɔmanw dɔrɔn de bɛ u la . O de kama a bɛ fɔ ko bana in bɛ mɔgɔ tan o tan na, kelen dɔrɔn de bɛ sɔrɔ. Mɔgɔ caman bɛ ɲɛnamaya kɛ cogo bɛnnen na, kɛnɛya la, k’a sɔrɔ u yɛrɛ t’a dɔn ko bana in bɛ u la.

Nka, mɔgɔ dɔw bɛ se ka taamasiɲɛ dɔw sɔrɔ. Nin taamasiɲɛ ninnu bɛ se ka ɲɔgɔn ta mɔgɔ kelen-kelen bɛɛ la. An k’o taamasiɲɛw tila-tila kuluw ye.

Jogo suguya Fɛn minnu ka kan ka ye
Farikolo Taamaʃyɛnw

  • Ka janya ka tɛmɛ mɔgɔ hakɛ danma kan (kɛrɛnkɛrɛnnenya la ni sen janw) .
  • Ɲɛw ni ɲɔgɔn cɛ janya bɛ bonya dɔɔni
  • Ɲɛ kɔnɔna bɛ datugu ni fari ye (Epicanthal folds) .
  • Senw fla ye
  • Tuma dɔw la, bolokɔnincinin bɛ kɔrɔta dɔɔni.
  • Yɛlɛma misɛnniw bɛ kɛ barajuru cogoya la
  • A man teli, kirinni
  • Gɛlɛya minnu bɛ sɔrɔ sugunɛ walima kɔnɔbara la
  • Dusukun tantanni misɛnniw

Jogo minnu bɛ tali kɛ bonya, kalan ani hakili kɛnɛya la

  • Kuma ni kanko latɛmɛni
  • Kalanbaliya walima IQ ka dɔgɔn dɔɔni ka tɛmɛ balimakɛw kan
  • Jateminɛ-dɛsɛbana
  • Sosiyete ka sekow ni gɛlɛyaw ka ɲɛsin mɔgɔ wɛrɛw ma
  • Dɔ farala a ka teli ka bana dɔw sɔrɔ i n’a fɔ jɔrɔnanko ni degun
  • Yɛrɛbonya dɔgɔyali

K’a sɔrɔ nin taamasiɲɛ kelen walima caman bɛ aw den na, o kɔrɔ tɛ ko triple X syndrome bɛ a la. U bɛ se ka sɔrɔ fɛn caman wɛrɛw fɛ, o la ni haminanko dɔw bɛ aw la, a ka fisa aw ka kuma dɔgɔtɔrɔ dɔ fɛ.

Aw bɛ nin bana in dɔn cogo di?

Tuma caman na, o bana in bɛ sɔrɔ a danma. Misali la, a bɛ se ka sɔrɔ ni muso bɛ fura ɲini gɛlɛya dɔ la i n’a fɔ bange gɛlɛya walima kalolabɔ joona.

Fɛɛrɛ wɛrɛw ye:

  • Sɛgɛsɛgɛli minnu bɛ kɛ kɔnɔmaya waati : Jɛnɛya sɛgɛsɛgɛli i n’a fɔ NIPT (Non-Invasive Prenatal Testing) , Amniocentesis , walima CVS (Chorionic Villus Sampling) minnu bɛ kɛ denba kɔnɔma kan, olu bɛ se ka nin bana in dɔn sani den ka bange.
  • Joli sɛgɛsɛgɛliw : Den bangenen kɔfɛ, ni dɔgɔtɔrɔ bɛ sigasiga, kariyotipi sɛgɛsɛgɛli bɛ se ka kɛ walasa ka o dafa. Nin sɛgɛsɛgɛli in bɛ se k’a dɔn ni X kolosinsinnan wɛrɛ bɛ yen ani ni a bɛ farikolokisɛ kɛmɛsarada la joli la.

O furakɛcogo jumɛnw bɛ yen?

Fɛn fɔlɔ min ka kan ka to an hakili la, o ye ko jamu bana min bɛ wele ko Triple X Syndrome , o tɛ se ka kɛnɛya pewu.Sabula o ye fɛn ye min bɛ na ni an ka jeninida ye. Nka, ni a bɛ se ka gɛlɛyaw ni taamasiɲɛ minnu lase i ma, ni olu dɛmɛna ani k’u ɲɛnabɔ, i bɛ se ka ɲɛnamaya kɛ cogo la min bɛ bɛn pewu, ani ka ɲɛnamaya kɛ nisɔndiya la .

Furakɛli bɛ latigɛ ka kɛɲɛ ni mɔgɔ kelen-kelen bɛɛ ka bana taamasiɲɛw ni a magow ye.

  • Dɔgɔtɔrɔso lajɛw kɛli tuma bɛɛ: Dɔgɔtɔrɔ bɛ se ka sɛgɛsɛgɛliw kɛ i n’a fɔ ultrasound scan ani echocardiogramme (EKG) walasa ka gɛlɛya o gɛlɛya sɔrɔ sugunɛ, kɔnɔbara ani dusukun na.
  • Dɛmɛ baaradaw ni furakɛlicogo: Nin ye yɔrɔ ye min nafa ka bon kosɛbɛ.
  • Kuma ni kan furakɛli : O nafa ka bon kosɛbɛ denmisɛn minnu ka kuma bɛ mɛn.
  • Farikoloɲɛnajɛ furakɛcogo : A bɛ se ka dɛmɛ don ni farikolo fanga dɔgɔyara walima ni balansi gɛlɛyaw bɛ aw la.
  • Kalan dɛmɛni: Kalan gɛlɛya bɛ denmisɛn minnu na, olu bɛ se ka dɛmɛ kɛrɛnkɛrɛnnen sɔrɔ lakɔliso la.
  • Ladilikan: Ladilikan nafa ka bon kosɛbɛ jɔrɔnanko, degun, walima gɛlɛyaw ɲɛnabɔli la sigidamɔgɔw ni ɲɔgɔn cɛ jɛɲɔgɔnyaw la.
  • Ɔrimɔni furakɛli : Tuma dɔw la, dɔgɔtɔrɔ bɛ se ka fɛnw fɔ i n’a fɔ ɔrimɔni furakɛli walasa ka gɛlɛyaw furakɛ minnu bɛ sɔrɔ kɔnɔbara baara dɔgɔyali fɛ walima ka den janya kunbɛn.

Min nafa ka bon kosɛbɛ, o ye ka bana in dɔn joona ani ka dɛmɛ ni furakɛli wajibiyalenw kɛ walasa den ka se ka se a seko bɛɛ la.

Take-Home cikan

  • Triple X syndrome ye bana ye min bɛ sɔrɔ jamu fɛ, a bɛ npogotigininw dɔrɔn de minɛ, wa a bɛ kɛ k’a sɔrɔ a ma kɛ cogo si la. O tɛ mɔgɔ si ka jalaki ye.
  • Nin bana in bɛ musow ni npogotigi caman na, taamasiɲɛ foyi tɛ u la, wa u bɛ ɲɛnamaya kɛ cogo la min bɛ kɛnɛya pewu, min bɛ kɛ cogo la.
  • Hali ni fura kɛrɛnkɛrɛnnen tɛ o la, taamasiɲɛ o taamasiɲɛ bɛ sɔrɔ (kuma gɛlɛya, kalan gɛlɛya, hakili gɛlɛya) bɛ se ka ɲɛnabɔ ka ɲɛ ni furakɛli ni dɛmɛ ye.
  • Ni haminanko walima ɲininkali dɔw bɛ aw den ka yiriwali, a kɛcogo, walima a ka kalan kan, aw kana siran ka kuma aw ka dɔgɔtɔrɔ fɛ. K’a dɔn joona ani ka dɛmɛ don, o de ye fɛn ɲumanw ye minnu bɛ se ka kɛ.

Triple X Syndrome, 47,XXX, bana minnu bɛ sɔrɔ jamu fɛ, kolosinsinnanw, npogotigininw ka kɛnɛya, yiriwali gɛlɛyaw, kalanbaliya
⚠️ 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: 7 + 1 =