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Yala bana caman bɛ den na waati kelen na wa? An ka kuma DiGeorge Syndrome kan

Yala bana caman bɛ den na waati kelen na wa? An ka kuma DiGeorge Syndrome kan

Yala kɛnɛyako gɛlɛya ka ca ni kelen ye i denmisɛnnin na wa? N’a sɔrɔ i ye dusukun gɛlɛya dɔ kɔlɔsi, bana minnu bɛ to ka kɛ, walima minnu bɛ mɛn sen na. O gɛlɛya minnu bɛ iko u ni ɲɔgɔn cɛ tɛ kelen ye, olu caman bɛ se ka kɛ sababu kelen ye. O ye jamu cogoya kelen ye an bɛna kuma min kan bi. A bɛ fɔ a ma ko DiGeorge Syndrome.

N’an y’a fɔ cogo nɔgɔman na, DiGeorge Syndrome ye mun ye?

Nin ye bana ye min bɛ sɔrɔ jamu fɛ . An farikolo bɛ kɛ ni selilɛriw ye. Fɛn dɔ bɛ selilɛri kelen-kelen bɛɛ la min bɛ wele ko kolosinsinnan. Aw ka miiri ninnu na iko gafe belebelebaw minnu bɛ an farikolo fɛn bɛɛ dilancogo sɛbɛn. O la, nin cogoya in bɛ Kɛ ni nin gafe in yɔrɔ fitinin dɔ, i n’a fɔ ɲɛ dɔ, min bɛ Weele ko chromosome 22, o tɛ yen. Walasa ka tiɲɛ fɔ, o bɛ wele fana ko 22q11.2 deletion syndrome . O kɔrɔ ye ko yɔrɔ min bɛ Weele ko 11,2, o bɛ bolokɔni jan kan min bɛ Weele ko ‘q’, kolosinsinnan 22nan na, o tɛ yen.

Ni o jɛnɛya yɔrɔ fitinin in tununna, o bɛ nɔ bila den farikolo yɔrɔ caman falenni n’u ka baara la. Den dɔw bɛ bana dɔɔni de sɔrɔ, ka sɔrɔ dɔw fana bɛ se ka kɛ dɔɔni. A tɛ kelen ye den ni den cɛ. Hali ni fura dafalen tɛ o la, an bɛ se ka bana taamasiɲɛw kunbɛn ani ka den dɛmɛ a ka ɲɛnamaya kɛ cogo ɲuman na.

Taamasiɲɛ jumɛnw bɛ ye nin bana in na?

Nin bana in bɛ denmisɛn minnu na, olu bɛɛ tɛ kelen ye. A bɛ se ka kɛ denmisɛn dɔw tɛ bana taamasiɲɛ si jira fewu. Dɔ wɛrɛw bɛ se ka taamasiɲɛw jira minnu bɛ farikolo yɔrɔ caman minɛ. An ka gɛlɛya kunbabaw lajɛ minnu bɛ ye.

Farikolo sigicogo min bɛ nɔ bila Taamasiɲɛ minnu bɛ se ka ye
Dusukun Gɛlɛyaw
  • Dusukunnabana bangenenw (misali la, dingɛ dɔ bɛ dusukun kɔnɔna yɔrɔw ni ɲɔgɔn cɛ).
  • A ka gɛlɛn dusukun ma ka farikolo mago bɛ oksizɛni hakɛ min na, o pɔnpe.
  • Gɛlɛya minnu bɛ joli bɔcogo la ka bɔ dusukun na.
  • Aorta, n’o ye joli siraba belebeleba ye, o tɛ yiriwa ka ɲɛ.
Banakisɛfagalanw (Immune Deficiency) .
  • Banakisɛ minnu bɛ sɔrɔ tuma caman.
  • Joli kuru finman minnu bɛ banakisɛw kɛlɛ, olu hakɛ dɔgɔyali.
  • Timisi gland min nafa ka bon farikolo tangacogo la, o tɛ yiriwa ka ɲɛ walima a ka dɔgɔn kosɛbɛ.
  • Ɲɛda cogoya danfaralenw
  • Dawolo ni dawolo faralen don ɲɔgɔn kan.
  • Ɲɛkisɛw bɛ i n’a fɔ u datugulen don dɔɔni (ɲɛkisɛ minnu bɛ ni kuru ye).
  • Ɲɛda fla.
  • Nu sanfɛla bɛ bonya dɔɔni.
  • Dawolo tɛ yiriwa ka ɲɛ.
  • Yɛlɛma bɛ don tulolabanaw cogoya la.
  • Sugunɛ yiriwali ni kalan (Cognitive Issues) .
  • Kalanbaliya minnu bɛ sɔrɔ.
  • Kuma ni kanko latɛmɛni.
  • Motɛri ɲumanw ka seko ni dɔnko latɛmɛni.
  • Jateminɛ gɛlɛyaw (Attention-deficit/hyperactivity disorder - TDAH).
  • Bana minnu bɛ i n’a fɔ autizmu (Autisme spectre disorder).
  • Hakilila-kɛnɛya gɛlɛyaw.
  • Taamaʃyɛn ni taamasiɲɛ wɛrɛw
  • Kolo gɛlɛyaw (misali la, mɔgɔ janya ka surun, sɔgɔsɔgɔninjɛ).
  • Lamɛnni ni yelibaliya.
  • Ninakili gɛlɛya.
  • Kalisiyɔmu hakɛ dɔgɔyali joli la (kalisiyɔmu dɔgɔyali).
    • Gɛlɛya minnu bɛ sɔrɔ sugunɛ jɔcogo n’a baarakɛcogo la.
    • Gɛlɛya minnu bɛ sɔrɔ ɔrimɔni na.
    • Sin dili gɛlɛya denyɛrɛni waati.

    Mun na o bɛ kɛ denmisɛnnin na? O kun ye mun ye?

    I n’a fɔ an y’a ɲɛfɔ cogo min na ka tɛmɛ, o bɛ sɔrɔ kolosinsinnan 22 yɔrɔ fitinin dɔ bɔnɛni fɛ.Kunba fila bɛ yen minnu b’a to o bɛ kɛ.

    1. Ko min kɛra k’a sɔrɔ a ma kɛ k’a sɔrɔ a ma kɛ cogo si la: Nin de ka teli ka kɛ (9 10 kan) . Ni den kɔnɔma donna, o kɔrɔ ye ko siɲɛ fɔlɔ min na ba kɔnɔbara ni fa ka cɛya bɛ fara ɲɔgɔn kan, o kolosinsinnan yɔrɔ in bɛ se ka tunun bala la. Nin ye ko ye min bɛ kɛ k’a sɔrɔ a ma kɛ cogo si la.

    2. A bɛ ciyɛn sɔrɔ bangebagaw fɛ: A man ca kosɛbɛ (10 o 10 ɲɔgɔn) .Den bɛ se ka nin bana in ciyɛn ta ba walima fa fɛ min bɛ a la. A bɛ ciyɛn sɔrɔ ``autosomal dominant`` cogo la. O kɔrɔ ye ko hali ni o bana bɛ bangebaga dɔ la, a ka c’a la, den bɛna o bana sɔrɔ.

    Min nafa ka bon kosɛbɛ, o ye nin ye. A ka ca a la, nin ye ko ye min bɛ kɛ k’a sɔrɔ a ma kɛ cogo si la, o la aw kana aw dusu tiɲɛ, k’a miiri ko aw ye fɛn o fɛn kɛ walima aw ma fɛn o fɛn kɛ aw kɔnɔmaya waati, o de sababu ye. Nin tɛ i ka hakɛ ye fewu.

    Dɔgɔtɔrɔw bɛ o sɔrɔ cogo di?

    Tuma dɔw la, jiginni ɲɛfɛ sɛgɛsɛgɛliw bɛ se ka taamasiɲɛw di bana in kan. Misali la, a bɛ se ka sɔrɔ jiginni ɲɛfɛ ultrasound kɛtuma na walima sɛgɛsɛgɛli kɛrɛnkɛrɛnnen dɔ senfɛ i n’a fɔ kɔnɔbara basigilen.

    Nka, a ka ca a la, o bɛ sɔrɔ den bangenen kɔ dɔrɔn. Ni dɔgɔtɔrɔ bɛ den sɛgɛsɛgɛ, a bɛ se ka sigasiga o la ni a ye fɛn kɛrɛnkɛrɛnnenw ye den ɲɛda ni a tulo la. O kɔ, sɛgɛsɛgɛli caman bɛ kɛ walasa ka siga in dafa.

    Kɔrɔbɔliw bɛ kɛ o ko la

    • Echocardiogramme (Echocardiogramme): Sɛgɛsɛgɛli min bɛ kɛ walasa ka dusukun baaracogo n’a jɔcogo lajɛ.
    • Joli sɛgɛsɛgɛliw : Aw bɛ kalisiyɔmu hakɛ lajɛ joli la, ka joli jate dafalen kɛ (CBC) ani ka joli kuru finmanw hakɛ lajɛ.
    • Disi lajɛ : Aw bɛ thymus gland bonya lajɛ.
    • Sugunɛ ultrasound (Sugunɛ ka ultrasound).
    • Sɛgɛsɛgɛli kɛrɛnkɛrɛnnen minnu bɛ tali kɛ farikolo tangacogo la: Misali la, `Immunophenotyping` ani `Flow cytometry`.
    • Jɛnkulu sɛgɛsɛgɛli : O de bɛ a jira kɛrɛnkɛrɛnnenya la ni kolosinsinnan 22 yɔrɔ dɔ tɛ yen.

    O bɛ furakɛ cogo di?

    Jamu nafama min bɛ nin bana in bila mɔgɔ la, o tɛ se ka ban. Nka, taamasiɲɛw ni gɛlɛya minnu bɛ sɔrɔ a la , olu bɛ se ka furakɛ ka ɲɛ kosɛbɛ . Nin tɛ ko ye min bɛ se ka kɛ dɔgɔtɔrɔ kelen dɔrɔn fɛ. Fɛn suguya caman dɔnbagaw ka jɛkulu dɔ bɛ baara kɛ ɲɔgɔn fɛ walasa ka den furakɛ.

    Furakɛli kɛcogo tɛ kelen ye ka kɛɲɛ ni den ka bana taamasiɲɛw ye.

    • Banakisɛfagalanw bɛ di banakisɛw ma minnu bɛ to ka sɔrɔ.
    • Ni joli la kalisiyɔmu hakɛ ka dɔgɔn , kalisiyɔmu faralenw bɛ di a ma.
    • Lamɛnni gɛlɛyaw bɛ furakɛ ni tulolanɛgɛw walima mɛnnikɛminɛnw ye.
    • Kuma, farikoloɲɛnajɛ ani baara furakɛli bɛ kuma, taama ani baara wɛrɛw latɛmɛni furakɛ.
    • Ɔrimɔni sinsinni furakɛli bɛ kɛ ka ɔrimɔni gɛlɛyaw furakɛ .
    • Opereli bɛ se ka kɛ dusukun gɛlɛyaw walima dawolo faralen ɲɔgɔn kan.
    • Kalanbaliya bɛ denmisɛn minnu na, olu bɛ bila kalan kɛrɛnkɛrɛnnenw bolodalenw na lakɔliso la.

    Aw ka kan ka taa ni aw den ye dɔgɔtɔrɔso la tuma jumɛn?

    A ka ca a la, dɔgɔtɔrɔ bɛna o bana in dɔn bange waati walima sɛgɛsɛgɛli kɛcogo kɔrɔw senfɛ denmisɛnya waati. Nka, ni aw bɛ sigasiga ko an ye baro kɛ bana taamasiɲɛ minnu kan, olu dɔ bɛ aw den na, aw bɛ kuma aw ka dɔgɔtɔrɔ fɛ o yɔrɔnin bɛɛ.

    Kɛrɛnkɛrɛnnenya la, ni ninakili gɛlɛya dɔ bɛ aw den na, aw bɛ taa n’a ye dɔgɔtɔrɔso la min ka surun aw la, o yɔrɔ la, kɔrɔtɔko ɲɛmɔgɔso (ETU) la joona.

    I n’a fɔ bangebaga, i bɛ se ka dusukasi kosɛbɛ ani ka jɔrɔ kosɛbɛ ni i y’a dɔn ko bana dɔ bɛ i den ka jamu la i n’a fɔ DiGeorge Syndrome. O ye ko ye min tɛ kojugu ye. Nka aw hakili to a la ko ni furakɛli ni dɛmɛ ɲuman kɛra o denmisɛnw na, u bɛ se ka ɲɛnamaya kɛ ni timinandiya ye, ka ɲɛnamaya kɛ nisɔndiya la. Ni banaw ma kɛ minnu bɛ mɔgɔ ka ɲɛnamaya bila farati la i n’a fɔ dusukunnabana jugumanw, denmisɛn fanba bɛ se ka ɲɛnamaya kɛ cogo bɛnnen na.

    Take-Home cikan

    • DiGeorge ka bana ye bana ye min bɛ sɔrɔ jamu fɛ, min bɛ sɔrɔ kolosinsinnan 22 yɔrɔ fitinin dɔ bɔnɛni fɛ.
    • Tuma caman na, o ye ko ye min bɛ kɛ k’a sɔrɔ a ma kɛ cogo si la. O tɛ i ka hakɛ ye.
    • A taamasiɲɛw tɛ kelen ye kosɛbɛ den ni den cɛ. Dɔw bɛ se ka nɔ nɔgɔmanba bila, ka sɔrɔ dɔw bɛ se ka bana jugumanw sɔrɔ i n’a fɔ dusukunnabana.
    • Hali ni fura kɛrɛnkɛrɛnnen tɛ o la, bana taamasiɲɛw furakɛli bɛ se ka den dɛmɛ ka ɲɛnamaya kɛ kɛnɛya la, min bɛ baara kɛ.
    • Dɔgɔtɔrɔ kɛrɛnkɛrɛnnenw ka kulu dɔ ka dɛmɛ nafa ka bon o la. Aw bɛ kuma aw ka dɔgɔtɔrɔ fɛ k’a jɛya o ko la.

    DiGeorge Syndrome, 22q11.2 deletion syndrome, bana minnu bɛ sɔrɔ jamu fɛ, denmisɛnniw ka banaw, kolosinsinnan 22, dusukunnabana bangenen, farikolo tangalanw, yiriwali kɔtigɛ
    ⚠️ 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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    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: 3 + 8 =
    Yala bana caman bɛ den na waati kelen na wa? An ka kuma DiGeorge Syndrome kan

    Yala bana caman bɛ den na waati kelen na wa? An ka kuma DiGeorge Syndrome kan

    Yala kɛnɛyako gɛlɛya ka ca ni kelen ye i denmisɛnnin na wa? N’a sɔrɔ i ye dusukun gɛlɛya dɔ kɔlɔsi, bana minnu bɛ to ka kɛ, walima minnu bɛ mɛn sen na. O gɛlɛya minnu bɛ iko u ni ɲɔgɔn cɛ tɛ kelen ye, olu caman bɛ se ka kɛ sababu kelen ye. O ye jamu cogoya kelen ye an bɛna kuma min kan bi. A bɛ fɔ a ma ko DiGeorge Syndrome.

    N’an y’a fɔ cogo nɔgɔman na, DiGeorge Syndrome ye mun ye?

    Nin ye bana ye min bɛ sɔrɔ jamu fɛ . An farikolo bɛ kɛ ni selilɛriw ye. Fɛn dɔ bɛ selilɛri kelen-kelen bɛɛ la min bɛ wele ko kolosinsinnan. Aw ka miiri ninnu na iko gafe belebelebaw minnu bɛ an farikolo fɛn bɛɛ dilancogo sɛbɛn. O la, nin cogoya in bɛ Kɛ ni nin gafe in yɔrɔ fitinin dɔ, i n’a fɔ ɲɛ dɔ, min bɛ Weele ko chromosome 22, o tɛ yen. Walasa ka tiɲɛ fɔ, o bɛ wele fana ko 22q11.2 deletion syndrome . O kɔrɔ ye ko yɔrɔ min bɛ Weele ko 11,2, o bɛ bolokɔni jan kan min bɛ Weele ko ‘q’, kolosinsinnan 22nan na, o tɛ yen.

    Ni o jɛnɛya yɔrɔ fitinin in tununna, o bɛ nɔ bila den farikolo yɔrɔ caman falenni n’u ka baara la. Den dɔw bɛ bana dɔɔni de sɔrɔ, ka sɔrɔ dɔw fana bɛ se ka kɛ dɔɔni. A tɛ kelen ye den ni den cɛ. Hali ni fura dafalen tɛ o la, an bɛ se ka bana taamasiɲɛw kunbɛn ani ka den dɛmɛ a ka ɲɛnamaya kɛ cogo ɲuman na.

    Taamasiɲɛ jumɛnw bɛ ye nin bana in na?

    Nin bana in bɛ denmisɛn minnu na, olu bɛɛ tɛ kelen ye. A bɛ se ka kɛ denmisɛn dɔw tɛ bana taamasiɲɛ si jira fewu. Dɔ wɛrɛw bɛ se ka taamasiɲɛw jira minnu bɛ farikolo yɔrɔ caman minɛ. An ka gɛlɛya kunbabaw lajɛ minnu bɛ ye.

    Farikolo sigicogo min bɛ nɔ bila Taamasiɲɛ minnu bɛ se ka ye
    Dusukun Gɛlɛyaw
    • Dusukunnabana bangenenw (misali la, dingɛ dɔ bɛ dusukun kɔnɔna yɔrɔw ni ɲɔgɔn cɛ).
    • A ka gɛlɛn dusukun ma ka farikolo mago bɛ oksizɛni hakɛ min na, o pɔnpe.
    • Gɛlɛya minnu bɛ joli bɔcogo la ka bɔ dusukun na.
    • Aorta, n’o ye joli siraba belebeleba ye, o tɛ yiriwa ka ɲɛ.
    Banakisɛfagalanw (Immune Deficiency) .
  • Banakisɛ minnu bɛ sɔrɔ tuma caman.
  • Joli kuru finman minnu bɛ banakisɛw kɛlɛ, olu hakɛ dɔgɔyali.
  • Timisi gland min nafa ka bon farikolo tangacogo la, o tɛ yiriwa ka ɲɛ walima a ka dɔgɔn kosɛbɛ.
  • Ɲɛda cogoya danfaralenw
  • Dawolo ni dawolo faralen don ɲɔgɔn kan.
  • Ɲɛkisɛw bɛ i n’a fɔ u datugulen don dɔɔni (ɲɛkisɛ minnu bɛ ni kuru ye).
  • Ɲɛda fla.
  • Nu sanfɛla bɛ bonya dɔɔni.
  • Dawolo tɛ yiriwa ka ɲɛ.
  • Yɛlɛma bɛ don tulolabanaw cogoya la.
  • Sugunɛ yiriwali ni kalan (Cognitive Issues) .
  • Kalanbaliya minnu bɛ sɔrɔ.
  • Kuma ni kanko latɛmɛni.
  • Motɛri ɲumanw ka seko ni dɔnko latɛmɛni.
  • Jateminɛ gɛlɛyaw (Attention-deficit/hyperactivity disorder - TDAH).
  • Bana minnu bɛ i n’a fɔ autizmu (Autisme spectre disorder).
  • Hakilila-kɛnɛya gɛlɛyaw.
  • Taamaʃyɛn ni taamasiɲɛ wɛrɛw
  • Kolo gɛlɛyaw (misali la, mɔgɔ janya ka surun, sɔgɔsɔgɔninjɛ).
  • Lamɛnni ni yelibaliya.
  • Ninakili gɛlɛya.
  • Kalisiyɔmu hakɛ dɔgɔyali joli la (kalisiyɔmu dɔgɔyali).
    • Gɛlɛya minnu bɛ sɔrɔ sugunɛ jɔcogo n’a baarakɛcogo la.
    • Gɛlɛya minnu bɛ sɔrɔ ɔrimɔni na.
    • Sin dili gɛlɛya denyɛrɛni waati.

    Mun na o bɛ kɛ denmisɛnnin na? O kun ye mun ye?

    I n’a fɔ an y’a ɲɛfɔ cogo min na ka tɛmɛ, o bɛ sɔrɔ kolosinsinnan 22 yɔrɔ fitinin dɔ bɔnɛni fɛ.Kunba fila bɛ yen minnu b’a to o bɛ kɛ.

    1. Ko min kɛra k’a sɔrɔ a ma kɛ k’a sɔrɔ a ma kɛ cogo si la: Nin de ka teli ka kɛ (9 10 kan) . Ni den kɔnɔma donna, o kɔrɔ ye ko siɲɛ fɔlɔ min na ba kɔnɔbara ni fa ka cɛya bɛ fara ɲɔgɔn kan, o kolosinsinnan yɔrɔ in bɛ se ka tunun bala la. Nin ye ko ye min bɛ kɛ k’a sɔrɔ a ma kɛ cogo si la.

    2. A bɛ ciyɛn sɔrɔ bangebagaw fɛ: A man ca kosɛbɛ (10 o 10 ɲɔgɔn) .Den bɛ se ka nin bana in ciyɛn ta ba walima fa fɛ min bɛ a la. A bɛ ciyɛn sɔrɔ ``autosomal dominant`` cogo la. O kɔrɔ ye ko hali ni o bana bɛ bangebaga dɔ la, a ka c’a la, den bɛna o bana sɔrɔ.

    Min nafa ka bon kosɛbɛ, o ye nin ye. A ka ca a la, nin ye ko ye min bɛ kɛ k’a sɔrɔ a ma kɛ cogo si la, o la aw kana aw dusu tiɲɛ, k’a miiri ko aw ye fɛn o fɛn kɛ walima aw ma fɛn o fɛn kɛ aw kɔnɔmaya waati, o de sababu ye. Nin tɛ i ka hakɛ ye fewu.

    Dɔgɔtɔrɔw bɛ o sɔrɔ cogo di?

    Tuma dɔw la, jiginni ɲɛfɛ sɛgɛsɛgɛliw bɛ se ka taamasiɲɛw di bana in kan. Misali la, a bɛ se ka sɔrɔ jiginni ɲɛfɛ ultrasound kɛtuma na walima sɛgɛsɛgɛli kɛrɛnkɛrɛnnen dɔ senfɛ i n’a fɔ kɔnɔbara basigilen.

    Nka, a ka ca a la, o bɛ sɔrɔ den bangenen kɔ dɔrɔn. Ni dɔgɔtɔrɔ bɛ den sɛgɛsɛgɛ, a bɛ se ka sigasiga o la ni a ye fɛn kɛrɛnkɛrɛnnenw ye den ɲɛda ni a tulo la. O kɔ, sɛgɛsɛgɛli caman bɛ kɛ walasa ka siga in dafa.

    Kɔrɔbɔliw bɛ kɛ o ko la

    • Echocardiogramme (Echocardiogramme): Sɛgɛsɛgɛli min bɛ kɛ walasa ka dusukun baaracogo n’a jɔcogo lajɛ.
    • Joli sɛgɛsɛgɛliw : Aw bɛ kalisiyɔmu hakɛ lajɛ joli la, ka joli jate dafalen kɛ (CBC) ani ka joli kuru finmanw hakɛ lajɛ.
    • Disi lajɛ : Aw bɛ thymus gland bonya lajɛ.
    • Sugunɛ ultrasound (Sugunɛ ka ultrasound).
    • Sɛgɛsɛgɛli kɛrɛnkɛrɛnnen minnu bɛ tali kɛ farikolo tangacogo la: Misali la, `Immunophenotyping` ani `Flow cytometry`.
    • Jɛnkulu sɛgɛsɛgɛli : O de bɛ a jira kɛrɛnkɛrɛnnenya la ni kolosinsinnan 22 yɔrɔ dɔ tɛ yen.

    O bɛ furakɛ cogo di?

    Jamu nafama min bɛ nin bana in bila mɔgɔ la, o tɛ se ka ban. Nka, taamasiɲɛw ni gɛlɛya minnu bɛ sɔrɔ a la , olu bɛ se ka furakɛ ka ɲɛ kosɛbɛ . Nin tɛ ko ye min bɛ se ka kɛ dɔgɔtɔrɔ kelen dɔrɔn fɛ. Fɛn suguya caman dɔnbagaw ka jɛkulu dɔ bɛ baara kɛ ɲɔgɔn fɛ walasa ka den furakɛ.

    Furakɛli kɛcogo tɛ kelen ye ka kɛɲɛ ni den ka bana taamasiɲɛw ye.

    • Banakisɛfagalanw bɛ di banakisɛw ma minnu bɛ to ka sɔrɔ.
    • Ni joli la kalisiyɔmu hakɛ ka dɔgɔn , kalisiyɔmu faralenw bɛ di a ma.
    • Lamɛnni gɛlɛyaw bɛ furakɛ ni tulolanɛgɛw walima mɛnnikɛminɛnw ye.
    • Kuma, farikoloɲɛnajɛ ani baara furakɛli bɛ kuma, taama ani baara wɛrɛw latɛmɛni furakɛ.
    • Ɔrimɔni sinsinni furakɛli bɛ kɛ ka ɔrimɔni gɛlɛyaw furakɛ .
    • Opereli bɛ se ka kɛ dusukun gɛlɛyaw walima dawolo faralen ɲɔgɔn kan.
    • Kalanbaliya bɛ denmisɛn minnu na, olu bɛ bila kalan kɛrɛnkɛrɛnnenw bolodalenw na lakɔliso la.

    Aw ka kan ka taa ni aw den ye dɔgɔtɔrɔso la tuma jumɛn?

    A ka ca a la, dɔgɔtɔrɔ bɛna o bana in dɔn bange waati walima sɛgɛsɛgɛli kɛcogo kɔrɔw senfɛ denmisɛnya waati. Nka, ni aw bɛ sigasiga ko an ye baro kɛ bana taamasiɲɛ minnu kan, olu dɔ bɛ aw den na, aw bɛ kuma aw ka dɔgɔtɔrɔ fɛ o yɔrɔnin bɛɛ.

    Kɛrɛnkɛrɛnnenya la, ni ninakili gɛlɛya dɔ bɛ aw den na, aw bɛ taa n’a ye dɔgɔtɔrɔso la min ka surun aw la, o yɔrɔ la, kɔrɔtɔko ɲɛmɔgɔso (ETU) la joona.

    I n’a fɔ bangebaga, i bɛ se ka dusukasi kosɛbɛ ani ka jɔrɔ kosɛbɛ ni i y’a dɔn ko bana dɔ bɛ i den ka jamu la i n’a fɔ DiGeorge Syndrome. O ye ko ye min tɛ kojugu ye. Nka aw hakili to a la ko ni furakɛli ni dɛmɛ ɲuman kɛra o denmisɛnw na, u bɛ se ka ɲɛnamaya kɛ ni timinandiya ye, ka ɲɛnamaya kɛ nisɔndiya la. Ni banaw ma kɛ minnu bɛ mɔgɔ ka ɲɛnamaya bila farati la i n’a fɔ dusukunnabana jugumanw, denmisɛn fanba bɛ se ka ɲɛnamaya kɛ cogo bɛnnen na.

    Take-Home cikan

    • DiGeorge ka bana ye bana ye min bɛ sɔrɔ jamu fɛ, min bɛ sɔrɔ kolosinsinnan 22 yɔrɔ fitinin dɔ bɔnɛni fɛ.
    • Tuma caman na, o ye ko ye min bɛ kɛ k’a sɔrɔ a ma kɛ cogo si la. O tɛ i ka hakɛ ye.
    • A taamasiɲɛw tɛ kelen ye kosɛbɛ den ni den cɛ. Dɔw bɛ se ka nɔ nɔgɔmanba bila, ka sɔrɔ dɔw bɛ se ka bana jugumanw sɔrɔ i n’a fɔ dusukunnabana.
    • Hali ni fura kɛrɛnkɛrɛnnen tɛ o la, bana taamasiɲɛw furakɛli bɛ se ka den dɛmɛ ka ɲɛnamaya kɛ kɛnɛya la, min bɛ baara kɛ.
    • Dɔgɔtɔrɔ kɛrɛnkɛrɛnnenw ka kulu dɔ ka dɛmɛ nafa ka bon o la. Aw bɛ kuma aw ka dɔgɔtɔrɔ fɛ k’a jɛya o ko la.

    DiGeorge Syndrome, 22q11.2 deletion syndrome, bana minnu bɛ sɔrɔ jamu fɛ, denmisɛnniw ka banaw, kolosinsinnan 22, dusukunnabana bangenen, farikolo tangalanw, yiriwali kɔtigɛ
    ⚠️ 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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