I tɛ se ka i ɲɛw kunbɛn ka ɲɛ ani i farikolo fan kelen bɛ paralize wa? An ka kuma Weber Syndrome kan

Yala i delila ka miiri k’a sɔrɔ i tɛna i yɛrɛ minɛ yɔrɔnin kelen, ka i farikolo yɔrɔ dɔ walima i sen dɔ bɔ i fari fan dɔ la wa? Tiɲɛ na, nin ye ko ye min bɛ siran ani min tɛ se ka miiri, nka o ye fɛn ye an ka kan ka min kunbɛn tuma dɔw la an ka ɲɛnamaya kɔnɔ. Bi an bɛna kuma bana dɔ kan min man ca, bɛɛ ka kan ka min dɔn. dɔgɔtɔrɔw bɛ min wele ko Weber Syndrome , o ye nin ye .

Weber Syndrome ye mun ye tigitigi?

N’an y’a fɔ cogo nɔgɔman na, Weber Syndrome ye bana ye min bɛ sɔrɔ i cɛmancɛ-sɔgɔsɔgɔninjɛ tiɲɛni fɛ . Cɛmancɛ-sɔgɔsɔgɔninjɛ ye bɔrɔ nafama ye min bɛ cikanw ta ka bɔ i kunkolo la ka taa i kɔkolo la. O ye i kunkolo yɔrɔ ye min bɛ i kunkolo sanfɛ. Kunsɛmɛnasumaya nafama fila minnu bɛ fɛnw kɔlɔsi i n’a fɔ i ɲɛw lamagacogo ani i ɲɛkisɛw kɔrɔtacogo— ɲɛkisɛw ni ɲɛkisɛw — olu bɛ daminɛ cɛmancɛ-sɔgɔsɔgɔninjɛ la.

O la, ni nin cɛmancɛ-sɔgɔsɔgɔninjɛ in tiɲɛna cogo o cogo, aw bɛna hemiplegie , o kɔrɔ ye ko aw tɛna se ka aw farikolo fan kelen minɛ tuguni. O waati kelen na, aw bɛna gɛlɛyaw sɔrɔ ɲɛ ni yeli la fan dɔ fɛ. O de bɛ ye kosɛbɛ Weber Syndrome la. O bɛ jate bana ye min man ca kosɛbɛ .

Kunsɛmɛ cɛmancɛ tiɲɛni sababu min ka teli ka kɛ, o ye sɔgɔsɔgɔninjɛ ye , o min ye joli bɔli barika la ka taa kunsɛmɛ na. Nka, a bɛ se ka kɛ fana kun wɛrɛw la.

O taamasiɲɛw ye mun ye? An b’a dɔn cogo di?

Taamasiɲɛba caman bɛ yen minnu bɛ se ka ye Weber Syndrome la. U ye:

• Ɲɛkisɛ min bɛ jigin (ptose) ɲɛ kelen na . A bɛ i n’a fɔ ɲɛ tilalen don.
• Ɲɛ min bananen don, o bɛ se ka jigin ka taa kɛnɛma , o kɔrɔ ye ko ɲɛ tɛ se ka kunbɛn ka ɲɛ.
• Fɛn fila yecogo siɲɛ kelen (diplopie) . O bɛ wele ko yeli fila.
• Bolo ni senw farikolo fan kelen na, a yɔrɔ dɔ walima a dafalen . O bɛ kɛ ɲɛ min bananen don, o fan dɔ fɛ.

A nafa ka bon kosɛbɛ: Ni aw ye nin taamasiɲɛ kelen walima caman sɔrɔ, walima ni kirinni taamasiɲɛ caman wɛrɛw dɔ ye aw ye , i n’a fɔ kumabaliya , dusukunnataw tiɲɛni , yelibaliya , balansi koɲɛw , walima ɲɛda sɔgɔsɔgɔninjɛ , aw ka kan ka taa dɔgɔtɔrɔso la joona. O bɛ se ka kɛ ɲɛnamaya walima saya ko ye.

Tuma dɔw la, Weber Syndrome bɛ mɔgɔ minnu na, olu bɛ...Balan ni ɲɔgɔndɛmɛ gɛlɛyaw (ataxia) , o kɔrɔ ye ko taama ni fɛnw minɛni gɛlɛya, olu fana bɛ se ka sɔrɔ.

A ka ca a la, ni Weber Syndrome bɛ yen a kelen na, o tɛ nɔ bila aw ka miirili (hakilila, hakili) la . Nka, ni tiɲɛni min kɛra kunsɛmɛ yɔrɔ wɛrɛw la, o jɛnsɛnna, taamasiɲɛ wɛrɛw bɛ se ka ye. Misali la, Weber Syndrome bɛ se ka kɛ tuma dɔw la ni pons (pons) paralizi ye, o min ye kunsɛmɛnasumaya yɔrɔ dɔ ye. O cogo la, taamasiɲɛ wɛrɛw fana bɛ se ka ye.

Weber Syndrome sababuw ye mun ye?

Weber Syndrome bɛ sɔrɔ joginda fɛ min bɛ aw cɛmancɛ kunsɛmɛ yɔrɔ kɛrɛnkɛrɛnnen dɔ la, min bɛ kɛ kɔnɔbara cɛmancɛ la. Nin tiɲɛni suguya in sababuba ye :

• Sɔgɔsɔgɔninjɛ: O de ka teli ka kɛ a sababu ye. A bɛ se ka sɔrɔ joli sira dɔ datugulen walima a karilen fɛ min bɛ joli lase o kunsɛmɛ yɔrɔ ma.
• Sugunɛbilenni (joli sira dɔ wulicogo ni a pɛrɛnni kunsɛmɛ na).
• Joli bɔli kunsɛmɛ na.
• Sugunɛbilenni.
• Bana minnu bɛ miyɛlini bɔ , i n’a fɔ Sklerose Multiple, olu bɛ miyɛlini dawolo tiɲɛ farikolo yɔrɔw lamini na.

Jɔn de ka teli ka nin ko in sɔrɔ? (Fara minnu bɛ a la) .

I n’a fɔ an y’a ɲɛfɔ cogo min na ka tɛmɛ, Weber Syndrome sababuba ye sɔgɔsɔgɔninjɛ ye, o la, farati kelen minnu bɛ kirinni nɔ bila, olu fana bɛ nɔ bila a la. Nin don:

• Tansiyɔn jiginni (Tansiyɔn jiginni / Tansiyɔn jiginni).
• Kɔlɔsili hakɛ caya joli la (Kɔlɔsili hakɛ caman / Hyperlipidemia).
• Jabɛti.
• Sigarɛtimin.

Ni nin farati ninnu dɔ walima u caman bɛ aw la, a nafa ka bon kosɛbɛ ka dɔgɔtɔrɔw ka ladilikanw sɔrɔ tuma bɛɛ ani ka u kunbɛn. O kɛli bɛ se ka dɔ bɔ bana dɔw sɔrɔli la i n’a fɔ farikolojidɛsɛ ani Weber Syndrome.

Dɔgɔtɔrɔw bɛ o sɛgɛsɛgɛ cogo di? (Sɛgɛsɛgɛli) .

Ni taamasiɲɛw bɛ aw la minnu bɛ tali kɛ Weber Syndrome la, dɔgɔtɔrɔw bɛna a ɲini fɔlɔ ka a dɔn ni kirinni bɛ aw la. O bɛ kɛ barisa furakɛli teliya de nafa ka bon kosɛbɛ. Walisa k’o kɛ:

• hakililata sɛgɛsɛgɛli dafalen bɛna kɛ i farikolo la .
• Sugunɛ CT scan bɛ kɛ o yɔrɔnin bɛɛ.
• Tuma dɔw la, a bɛ se ka kɛ fana ko sɛgɛsɛgɛli wɛrɛ ka kɛ walasa ka joli siraw sɛgɛsɛgɛ kunkolo ni kɔ la ani ka MRI sɛgɛsɛgɛli kɛ kunsɛmɛ na.

Ni aw ka bana taamasiɲɛw ni o sɛgɛsɛgɛliw y’a jira ko tiɲɛni kɛra aw cɛmancɛ la, dɔgɔtɔrɔw bɛna a fɔ ko Weber Syndrome bɛ aw la.

O furakɛcogo ye mun ye?

Ni aw bɛ Weber Syndrome furakɛ, aw bɛ sinsin fɔlɔ kɛ a sababu basigilen furakɛli kan (a ka ca a la a bɛ kɛ jolida ye). Aw ka dɔgɔtɔrɔso jɛkulu bɛna aw ka fiɲɛbɔyɔrɔw ɲɛnabɔ joona ani ka joli lasegin aw hakili la. Tuma dɔw la , kunsɛmɛ opereli (sɔgɔsɔgɔninjɛ) fana bɛ se ka kɛ wajibi ye.

Labɛnni fɛɛrɛw ye furakɛli kunbaba ye min bɛ kɛ kɛrɛnkɛrɛnnenya la Weber Syndrome la.

Rehabilitation ye mun ye? O nafa ka bon cogo di?

Labɛnni ye kɛnɛyako yɔrɔ nafamaba ye mɔgɔ caman bolo minnu ye sɔgɔsɔgɔninjɛ sɔrɔ. O ye ka i dɛmɛ ka seko minnu bɔnɛ i hakili la, i ka olu sɔrɔ kokura, walima k’i dɛmɛ ka ɲɛnamaya kɛ ni fɛn caman yeli ye. AVC furakɛli jɛkulu walima farikoloɲɛnajɛla min kalanna kɛrɛnkɛrɛnnenya la, o bɛ se k’aw dɛmɛ o la. A ka fisa ka nin kɛnɛyako porogaramu in daminɛ joona.

Weber Syndrome ni cɛmancɛ-sɔgɔsɔgɔninjɛ furakɛcogo bɛ se ka kɛ ninnu ye:

• Farikoloɲɛnajɛ minnu bɛ dɛmɛ ka farikolo yɔrɔ dɔ lamaga (Range-of-motion exercises) .
• Degeli minnu bɛ kɛ walasa ka balansi ni ɲɔgɔndɛmɛ ɲɛ.
• Aw bɛ aw ɲɛw lajɛ ani ka farikoloɲɛnajɛ ɲumanw kɛ walasa ka yeli fila dɔgɔya.
• A bɛ se ka kɛ mɔgɔ dɔw tɛ se ka u ka sugunɛ kunbɛn (sugunɛbaliya). Kalan kɛrɛnkɛrɛnnen ka kan ka kɛ o kama (Sugunɛbilenni kalan) .
• Fura ni fɛɛrɛ wɛrɛw ka kan ka kɛ walasa ka kirinni farati minnu bɛ yen, olu kɔlɔsi ani ka kirinni nataw bali.

A bɛna waati joli ta walasa ka kɛnɛya ka bɔ nin bana in na? (Aw ka kɛnɛyako jigiya) .

Fɛn caman bɛ nɔ bila Weber Syndrome bɛ mɔgɔ min na, o ka ɲɛnamaya ɲɛfɔcogo la, i n’a fɔ:

• O kun ye mun ye?
• Aw ye furakɛli sɔrɔ joona cogo min na .
• Yala Weber Syndrome dɔrɔn de bɛ aw la wa, walima aw kunkolo yɔrɔ wɛrɛw fana tiɲɛna wa ?
• aw bɛ ka baara kɛ ka ɲɛ cogo min na walasa ka paralizi nataw bali .

Weber Syndrome kelen bɛ mɔgɔ minnu na, ni u kunkolo tiɲɛni wɛrɛw tɛ, a ka ca a la, u ka ɲɛnamaya ɲɛfɔcogo ka ɲi . Ani fana, ka kɛnɛyako daminɛ joona , o nafa ka bon kosɛbɛ kɛnɛyako la.

Ni mɔgɔ dɔw labɛnna kokura, u bɛ se ka baara dɔw sɔrɔ kokura u farikolo yɔrɔw ni u ɲɛw la minnu bananen don. Nka, dɔw bɛ se ka gɛlɛya banbali sɔrɔ u lamagacogo la ani hakili gɛlɛya wɛrɛw.

Aw ka dɔgɔtɔrɔso jɛkulu bɛna se ka hakilina jɛlen di aw ma aw bɛ se ka min makɔnɔ ka da aw ka bana kan.

Gɛlɛya wɛrɛ jumɛnw bɛ se ka sɔrɔ ka a sababu kɛ Weber Syndrome ye?

Weber Syndrome ka teli ka gɛlɛyaw lase mɔgɔ ma, kɛrɛnkɛrɛnnenya la ni aw bɛ dilan kan. O de kama aw ka dɔgɔtɔrɔso jɛkulu bɛna a ɲini ka aw bila ka taa teliya la ani lafiya la. Gɛlɛya minnu bɛ se ka sɔrɔ olu dɔw ye:

• farikolo gɛlɛyali ni a sɔgɔsɔgɔninjɛ .
• Dilanw .
• Sɔgɔsɔgɔninjɛ bɛ sɔrɔ ni dumuni walima minfɛn donna fiɲɛbɔyɔrɔ la ka fogonfogonlabana bila mɔgɔ la.
• Joli bɛ kɛ senw ka jolisira jugumanw na (Trombose de la veine profonde - DVT) .
• O joli kurulen bɛ taa fogonfogon la (fogonfogon la sɔgɔsɔgɔninjɛ) .
• Sugunɛbilenniw (UTI) .

A laban na, fɛn min nafa ka bon kosɛbɛ, an ka kan ka to an hakili la

Atɛki bɛ se k’i ka ɲɛnamaya wuli yɔrɔnin kelen. O la, a nafa ka bon kosɛbɛ ka a taamasiɲɛw dɔn kosɛbɛ ani ka taa dɔgɔtɔrɔso la joona ni o taamasiɲɛ suguw ye aw walima aw gɛrɛgɛrɛ mɔgɔ dɔ la. Weber Syndrome bɛ se ka kɛ bana ye min man teli ka sɔrɔ, wa aw bɛ siran ani ka hami ni aw ye o ko mɛn. Nka aw hakili to fɛn kelen na, aw ka dɔgɔtɔrɔso jɛkulu labɛnnen don tuma bɛɛ k’aw dɛmɛ ani ka kɛ aw fɛ aw ka kɛnɛya taama na. O la sa, i hakili ka sabati ani ka laadilikan dilenw labato.

` Weber Syndrome, paralysie, cerebral palsy, cɛmancɛ-sɔgɔsɔgɔninjɛ, ɲɛ taamasiɲɛw, hakilibanaw, kɛnɛya sabatili