Yala den sugunɛ tɛ baara kɛ ka ɲɛ wa? An k'an janto nin Potter Syndrome in na!

N’i ​​ye denba ye, n’a sɔrɔ i bɛ hami kosɛbɛ i den ka kɛnɛyako la, tiɲɛ tɛ? A ka ca a la ka i yɛrɛ ɲininka ni den bɛ ka bonya ka ɲɛ kɔnɔbara la ani ni fɛn bɛɛ bɛ taa ɲɛ. Bi an bɛna kuma bana dɔ kan min man ca kosɛbɛ, bana min bɛ se ka denw minɛ. A bɛ fɔ a ma ko Potter Syndrome. Aw bɛ se ka hami ni aw ye nin kuma mɛn, nka a nafa ka bon kosɛbɛ aw ka aw janto o la.

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

Okey, an k'a tiɲɛ. Potter syndrome, n’a bɛ wele tuma dɔw la ko Potter sequence , o ye bana ye min man teli ka sɔrɔ, min bɛ nɔ bila den ka yiriwali la k’a sɔrɔ u bɛ kɔnɔbara la. o sababuba ye den sugunɛw tɛ yiriwa ka ɲɛ walima u ka baara bɛ tiɲɛ . Yala aw b’a dɔn ko ni den bɛ kɔnɔbara la, kɔnɔbara basigilen caman bɛ u lamini na wa. Sugunɛ jɔyɔrɔ ka bon nin kɔnɔbara basigilen in hakɛ kɔlɔsili la. O la ni sugunɛw ma baara kɛ ka ɲɛ, o kɔnɔbara basigilen in hakɛ bɛ dɔgɔya. Dɔgɔtɔrɔw b’o wele ko oligohydramnios.

A fɔ man di nka tuma dɔw la den bɛ bange ni sugunɛ fila tɛ a la, bana min bɛ wele ko ``Bilateral Renal Agenesis``, o bɛ se ka mɔgɔ faga. Nka, den dɔw bɛ se ka kisi ni u ka bana taamasiɲɛw man jugu walima ni ji bɔli ma juguya. Nka, o denw bɛ se ka fogonfogon ni sugunɛbaralabana basigilenw sɔrɔ ni u bɛ kɔrɔbaya.

A ka c’a la, o ko bɛna nɔ bila jɔn de la kosɛbɛ?

Tiɲɛ na, nin bana in min bɛ wele ko Potter syndrome, o bɛ se ka den bɛɛ minɛ. Sabula a bɛ tali kɛ kɔnɔbara basigilen na. Nka, sɛgɛsɛgɛli dɔw y’a jira ko den cɛmanw ka teli ka nin bana in sɔrɔ dɔɔni .

Yala Potter ka bana bɛ sɔrɔ cɛya la wa?

Nin ye ko gɛlɛn ye dɔɔnin. Potter syndrome tɛ bana ye min bɛ sɔrɔ jamu fɛ. Nka, bana dɔw bɛ yen minnu bɛ se ka kɛ sababu ye. An k’a lajɛ u ye fɛn minnu ye:

• Sugunɛbana min bɛ wele ko polycystique: O bɛ se ka sɔrɔ ba walima fa fɛ (autosomal dominant) walima bangebaga fila bɛɛ fɛ (autosomal recessive). O bɛ kɛ sababu ye ka kurukuruw sɔrɔ sugunɛ na.
• Sugunɛbilenni : O ye sugunɛw ka dɛsɛ ye. Tuma dɔw la, o bɛ se ka sɔrɔ fɛn caman cili fɛ FGF20 walima GREB1L jamu kɔnɔ. Nin bana in bɛ se ka ciyɛn ta cogo la min bɛ kɛ ni otosomali dominant ye walima otosomale recessive cogo la. O kɔrɔ ye ko den ka kan ka nin jamu jiginni in ciyɛn ta bangebaga kelen walima a fila bɛɛ fɛ.
• Yɛlɛma donna mɔgɔw la tuma dɔw la: Tuma dɔw la, jamu caman yeli k’a sɔrɔ u ma kɛ cogo si la, o bɛ se ka kɛ sababu ye ka Potter syndrome (Potter syndrome) bila mɔgɔ la, hali ni o bana ma sɔrɔ denbaya kɔnɔ mɔgɔ si la fɔlɔ.

Nin bana in ka ca cogo di?

Potter syndrome ye bana ye min man teli ka sɔrɔ . A jateminɛna ko nin bana in bɛ den kelen dɔrɔn de minɛ den 4000 fo 10000 la minnu bɛ bange. O la sa, i kana siran o ko mɛnni fɛ. Nka a nafa ka bon ka kɛ mɔgɔ hakili la.

Potter syndrome bɛ nɔ bila den farikolo la cogo di?

O de ye ko ye min nafa ka bon kosɛbɛ. Potter syndrome bɛ nɔ bila den kɔnɔna yɔrɔw, kɛrɛnkɛrɛnnenya la sugunɛ, u ka yiriwali ni u ka baara kɛcogo la . I n’a fɔ aw b’a dɔn cogo min na, sugunɛ ye farikolo yɔrɔ nafamaw ye minnu bɛ fɛnɲɛnamafagalanw ni ji wɛrɛw bɔ an farikolo la. Ni den bɛ kɔnɔbara la, sugunɛ bɛ sugunɛ bɔ. O sugunɛ bɛ segin ka kɛ kɔnɔbara basigilen ye.

O la, ni den sugunɛw tɛ baara kɛ ka ɲɛ, u tɛna kɔnɔbara basigilen caman bɔ ka u lamini. Nin kɔnɔbara basigilen in de bɛ den kuru. Ni o ji in tununna, den farikolo yɔrɔw ni a farikolo yiriwacogo bɛ nɔ bila a la. O kɔrɔ ye ko farikolo yɔrɔw tɛ yiriwa ka dafa . O tuma na fɛ, o farikolo yɔrɔw tɛ se k’u ka baara kɛ ka ɲɛ. O de bɛ na ni bana taamasiɲɛw ye minnu bɛ se ka mɔgɔ ka ɲɛnamaya bila farati la.

Potter syndrome taamasiɲɛw ye jumɛnw ye?

Potter syndrome taamasiɲɛw bɛ se ka ɲɔgɔn ta den ni den cɛ, wa a bana juguya bɛ se ka ɲɔgɔn ta. Nin taamasiɲɛ ninnu bɛ se ka nɔ bila aw ka kɔnɔmaya fana na, o bɛ se ka kɛ sababu ye ka jiginni kɛ ka kɔn a waati ɲɛ .

Denso kɔnɔji dɛsɛ

Kɔnɔmaya waati, ji jɛlen dɔ bɛ den lamini. Nin ye kɔnɔbara basigilen ye. O bɛ den tanga ani ka yɔrɔ di a ma a ka bonya. A bɛ kɛ balilan ye denso kogo ni den cɛ. Potter syndrome bɛ denmisɛn minnu na, olu tɛ nin kɔnɔbara basigilen in sɔrɔ, o la degun min bɛ bɔ denso kogo la, o bɛ nɔ bila den ka bonya cogo la.

Ɲɛda ni farikolo yɔrɔ kɛrɛnkɛrɛnnenw

Degun min bɛ sɔrɔ denso kɔnɔji dɛsɛ fɛ, o bɛ nɔ bila den farikolo yiriwacogo la. O bɛ se ka kɛ sababu ye ka ɲɛda cogoya kɛrɛnkɛrɛnnenw bila mɔgɔ la. O bɛ Weele ko "Potter facies" . O fɛnw ye:

• Dawolo tɛ yiriwa ka ɲɛ (a bɛ i n’a fɔ a bɛ wuli ka don a kɔnɔ).
• Ka kɛ ni kurukuru ye dawolo duguma duguma.
• Ɲɛw bilalen bɛ yɔrɔ jan.
• Naha dugu ka bridge (bonda) kɛra fla ye.
• Tulo minnu bɛ sigi ka dɔgɔn ani tulo kɔnɔ kolotugudaw dɔgɔyali.
• Fari bɛ kuru ɲɛkisɛw la.

O degun in bɛ se ka nɔ bila den farikolo yɔrɔ wɛrɛw yiriwali fana na. I n'a fo:

• Bolo ni senw surunyali.
• Sebaliya ka kolotugudaw janya ani ka u tilennen to ka ɲɛ, ani ka gɛlɛya (contractures).
• Den bonya ka dɔgɔn ni i y’a suma ni kɔnɔmaya si hakɛ ye.

Farikolo yɔrɔ minnu ma yiriwa walima minnu ma ɲɛ

Taamasiɲɛ minnu bɛ farikolo yɔrɔw minɛ, olu de bɛ mɔgɔ ka ɲɛnamaya bila farati la kosɛbɛ.. Potter syndrome la, den ka yiriwali bɛ nɔ bila a la, o la kɔnɔnafɛnw tɛ cikan walima waati sɔrɔ u mago bɛ minnu na walasa u ka yiriwa ka ɲɛ. Taamasiɲɛ minnu bɛ se ka sɔrɔ o sababu la, olu ye:

• Dusukun bana minnu bɛ sɔrɔ bangekɔlɔsi fɛ.
• Ɲɛbanaw (misali la ɲɛkisɛw, ɲɛkisɛw wulicogo).
• Sugunɛbanaw (sɔgɔsɔgɔninjɛ basigilen, sugunɛbilenni, sugunɛbilenni min bɛ wele ko polycystique).
• Fogonfogonlabanaw (fogonfogonlabana basigilen, ninakilidegun).

Sugunɛ falencogo juguman fana bɛ nɔ bila den kuraw ka sugunɛ hakɛ la. Nin fana ye taamasiɲɛ ye dɔgɔtɔrɔw bɛ min ɲini ni u bɛ Potter syndrome sɛgɛsɛgɛ.

Potter syndrome sababu ye mun ye?

Fɛn damadɔ bɛ yen minnu bɛ se ka kɛ sababu ye ka Potter syndrome (Potter syndrome) bila mɔgɔ la. U ye:

• Sugunɛ minnu tɛ yiriwa ka ɲɛ walima sugunɛ tɛ minnu na.
• Sugunɛbana min bɛ wele ko polycystique.
• Kɔnɔbara basigilen (Prune belly syndrome / Eagle-Barrett syndrome) .
• Sugunɛ siraw datugucogo.
• Denso kɔnɔji bɔli ka a sababu kɛ ɲɛgɛnɛsiraw karilen ye.
• Furakɛcogo minnu tɛ se ka kunbɛn ba la, misali la, sukarodunbana suguya fɔlɔ.

Nin taamasiɲɛ ninnu, kɛrɛnkɛrɛnnenya la minnu bɛ sugunɛ de minɛ, olu bɛ sɔrɔ barisa kɔnɔbara basigilen ji bɛrɛ tɛ kɔnɔbara la walasa ka den lamini .

Mun na o kɔnɔbara basigilen in bɛ ka dɔgɔya?

An ka nin ko in lajɛ ka ɲɛ dɔɔnin. a sababuba ye sugunɛw falencogo jugu ye .

Yala aw b’a dɔn ko kɔnɔmaya waati, den bɛ pan ji jɛlen dɔ la min ɲɛ ye jɛman ye, n’o bɛ wele ko kɔnɔbara basigilen. Nin ji in bɛ den tanga ani ka a dɛmɛ ka bonya aw kɔnɔmaya bɛɛ kɔnɔ wa? Aw ka kɔnɔmaya daminɛ na, nin kɔnɔbara basigilen in bɛ kɛ ni ji ni balofɛnw ye minnu bɛ bɔ aw fari la. Aw den bɛ nin kɔnɔbara basigilen in min. Dɔgɔkun 16 ni 20 cɛ, den bɛ daminɛ ka dɛmɛ don nin kɔnɔbara basigilen in na. I b’a dɔn cogo di? Ni koli bɛ kɛ! Aw den bɛ o jimafɛn in min ka sɔrɔ k’a bɔ a la ka kɛ sugunɛ ye. O bɛ Kɛ 'sèn kelen na.

O la, ni Potter syndrome bɛ aw den na, a ka sugunɛ kɛyɔrɔw, n’o ye sugunɛ ye, olu ma yiriwa ka ɲɛ, walima u tɛ yen, walima u tɛ baara kɛ. Ikomi den tɛ se ka koli kɛ, a tɛ se ka dɔ fara denso kɔnɔji hakɛ kan min b’a tanga. O de kama denso kɔnɔji ka dɔgɔn kɔnɔbara la.

Yala Potter syndrome suguya wɛrɛw bɛ yen wa?

Ɔwɔ, dɔgɔtɔrɔw bɛ Potter syndrome suguya wɛrɛw danfara, ka kɛɲɛ ni taamasiɲɛw ye minnu bɛ sugunɛ na.

• Classique Potter syndrome: Nin ye suguya ye min ka teli ka kɛ. A bɛ sɔrɔ ni den bangera ni sugunɛ fila bɛɛ tɛ a la.
• Potter syndrome suguya fɔlɔ:Nin bana suguya in bɛ sɔrɔ bana dɔ fɛ min bɛ wele ko sugunɛbana min bɛ wele ko polycystique sugunɛbana, o bɛ sɔrɔ bangebaga fila bɛɛ fɛ, wa o ye otosomali kɔsegin bana ye. O cogo la, kurukuruw bɛ sɔrɔ sugunɛ na.
• Potter syndrome type II : Nin bana suguya in bɛ sɔrɔ sugunɛbaralabanaw fɛ minnu bɛ kɛ kɔnɔbara la kɔnɔmaya waati.
• Potter syndrome type III : O fana bɛ sɔrɔ sugunɛbilenni fɛ, i n’a fɔ suguya fɔlɔ.Nka a bɛ sɔrɔ bangebaga kelen dɔrɔn de fɛ (Autosomal dominant).
• Potter syndrome type IV : Nin bana suguya in bɛ sɔrɔ sugunɛbaralabana (obstructive uropathy) fɛ ka a sababu kɛ den ka bonyabaliya ye kɔnɔbara la.

Potter syndrome bɛ sɔrɔ cogo di?

Potter syndrome bɛ se ka sɔrɔ kɔnɔmaya waati la , sɛgɛsɛgɛli fɛ sani bange ka kɛ . Taamaʃyɛn dɔ min b’a jira ko nin bana in bɛ se ka kɛ aw la kɔnɔmaya waati, o ye kɔnɔbara basigilen dɛsɛ ye den lamini na. Aw ka dɔgɔtɔrɔ bɛna o ɲini ultrasound scan kɛtuma na. U bɛna farikolo taamasiɲɛw fana ɲini i n’a fɔ kolotugudaw gɛlɛya (contractures).

Ni o ma dɔn sani den ka bange, dɔgɔtɔrɔ bɛ farikololajɛ kɛ den bangenen kɔfɛ walasa ka a taamasiɲɛw lajɛ. O taamasiɲɛw ye:

• Sugunɛ bɔli ka dɔgɔn kosɛbɛ.
• Ka ɲɛda cogoya kɛrɛnkɛrɛnnenw sɔrɔ.
• Ninakili gɛlɛya.

Sɛgɛsɛgɛli jumɛnw bɛ kɛ walasa ka o tiɲɛ?

Dɔgɔtɔrɔ bɛ se ka sɛgɛsɛgɛli caman kɛ walasa ka bana in sɛgɛsɛgɛ:

• Joli sɛgɛsɛgɛli jamu fɛ walasa ka jamu dɔn min bɛ bana taamasiɲɛw ɲɛnabɔ.
• Aw bɛ den fogonfogonw, a sugunɛw ani a sugunɛbara lajɛ ni ja sɛgɛsɛgɛliw ye i n’a fɔ X-ray, MRI walima ultrasound .
• Joli walima sugunɛ sɛgɛsɛgɛli walasa ka elekitoroliti ni anzimu hakɛ lajɛ.
• Echocardiogramme sɛgɛsɛgɛli min bɛ kɛ walasa ka dusukunnabana taamasiɲɛw lajɛ.

O furakɛcogo jumɛnw bɛ yen?

Potter syndrome furakɛli bɛ bɔ fogonfogon ni dusukun gɛlɛyaw juguya la (fogonfogon la sɔgɔsɔgɔninjɛ) minnu bɛ aw den sɔrɔ, ani sugandili minnu bɛ se ka kɛ walasa ka aw den ka sugunɛ baara dɛmɛ.

Aw ye miiri a la, aw den min bɛ ka bonya, o ka kan ka lamini ni kɔnɔbara basigilen ye kɔnɔmaya bɛɛ kɔnɔ walasa a fogonfogonw ka yiriwa ka ɲɛ. Ni den disi falen don ka mɛn kojugu, a bɛ se ka fogonfogon lamini caman bɔ a la walasa a ka se ka balo bange kɔfɛ.

Den kura min sugunɛbaralabana pewu, o furakɛli bɛ se ka gɛlɛya kosɛbɛ. Tuma dɔw la, ladonni gɛlɛnw kɛcogo dan ye ani den bangebagaw ladonni bɛ kɛ ka den ni bangebagaw to ɲɔgɔn fɛ ani ka den dusu saalo.Furakɛli kɛcogo fɛɛrɛw bɛ se ka kɛ sugandi ye.

Ni den bɛ balo bange kɔfɛ, furakɛli bɛna sinsin fɔlɔ bana taamasiɲɛw kunbɛnni kan minnu bɛ se ka a ka ɲɛnamaya bila farati la. O furakɛli ninnu bɛ se ka kɛ ninnu ye:

• Ninakili dɛmɛnanw tali (misali la fiɲɛbɔlan ).
• Fura minnu bɛ fogonfogon dɛmɛ, olu bɛ fogonfogon baara dɛmɛ.
• Opereli min bɛ kɛ ka sugunɛbaralabanaw dilan walima ka u bɔ.
• Opereli min bɛ kɛ walasa ka balocogo ɲɛ ka tɛmɛ balodɛsɛ furakɛli fɛ IV fɛ, kɔnɔbara basigilen fɛ, walima balodɛsɛ furakɛli fɛ.
• Dialyse ye fura ye min bɛ kɛ ka bagaw bɔ joli la minnu bɛ dalajɛ joli la ka a sababu kɛ sugunɛbilenni ye. Ni diyalizi furakɛli ma ɲɛ san damadɔ kɔfɛ, dɔgɔtɔrɔ bɛ se ka sugunɛ cili fɔ .

Ka kɛɲɛ ni den sɛgɛsɛgɛra waati ye, furakɛli bɛ se ka daminɛ kɔnɔmaya waati. Aw bɛ se ka furakɛli sɛgɛsɛgɛli fana kɛ, i n’a fɔ kɔnɔbara basigilen, o min bɛ ji fara aw ka kɔnɔbara basigilen kan walasa ka ji bila den lamini na. Nin furakɛli in bɛ baara kɛ ka ɲɛ sani kɔnɔmaya dɔgɔkun 22 ka se.

Yala Potter ka bana bɛ se ka bali wa?

A fɔ man di nka, fɛɛrɛ si tɛ yen min bɛ se ka Potter syndrome .

Ne ka kan ka mun makɔnɔ ni Potter syndrome bɛ ne den na?

Fura si tɛ Potter syndrome la. A ka ca a la, ni bana in sɔrɔla joona kɔnɔmaya waati, aw ka dɔgɔtɔrɔ bɛ se ka jiginni lafiyalen labɛn ani ka furakɛli kɛ walasa ka den dɛmɛ a ka ɲɛnamaya bange kɔfɛ.

Potter syndrome taamasiɲɛw bɛ mɔgɔ ka ɲɛnamaya bila farati la. Nka, fo ni den fogonfogonw ni a sugunɛw tiɲɛna kosɛbɛ, den ka ɲɛnamaya kɛcogo bɛ se ka ɲɛ dɔɔni.

Ikomi furakɛli bɛ daminɛ jiginni kɔfɛ dɔrɔn, furakɛli bɛɛ tɛ ɲɛ. A bɛ se ka kɛ ko u ka kan ka opereli caman kɛ u ka ɲɛnamaya daminɛ na.

Den min bɛ ni Potter syndrome ye, o ka ɲɛnamaya bɛ kɛ cogo di?

den minnu sɔrɔla ni Potter syndrome ye , olu si bɛ se ka surunya kosɛbɛ . O tɛ kelen ye bɛɛ la, wa a bɛ bɔ bana taamasiɲɛw de la. Ni bana taamasiɲɛw ka jugu, ani ni farikolo yɔrɔ kolomaw yiriwali ni u baara i n’a fɔ dusukun, fogonfogon ani sugunɛbaralabana, o kɔrɔfɔli tɛ ɲɛ. den fanba tɛ kisi u ka ɲɛnamaya tile fɔlɔw la . Ni bana misɛnniw don, ni bana taamasiɲɛw man jugu kosɛbɛ ani ni farikolo yɔrɔw ma nɔba bila, a si bɛ se ka janya dɔɔni.

Aw ka dɔgɔtɔrɔ bɛna kuma aw fɛ aw den ka bana sɛgɛsɛgɛli faratiw kan, ani a bɛna furaw fɔ aw ye minnu bɛ a si janya. Ni den ka bana sɛgɛsɛgɛli ka jugu, furakɛli kuntaalajan bɛ se ka kɛ fɛɛrɛ ye min bɛ se ka aw dɛmɛ ka dusukasi kunbɛn min bɛ sɔrɔ aw diyanyemɔgɔ dɔ la.Dusukasi walima dusukasi laadilikan fana bɛ se ka fɔ.

Tuma jumɛn na ne ka kan ka taa dɔgɔtɔrɔso la?

Ni aw ye fɛn dɔw kɔlɔsi aw ka kɔnɔmaya waati, kɛrɛnkɛrɛnnenya la ni den barika banna ka lamaga dabila a lamagacogo ɲuman kɔfɛ , aw bɛ taa dɔgɔtɔrɔso la o yɔrɔnin bɛɛ. Aw bɛ se ka den bange joona ka tɛmɛ a tun bɛ miiri min na. O la, a nafa ka bon kosɛbɛ ka to ka jiginni ɲɛfɛ sɛgɛsɛgɛliw kɛ ni dɔgɔtɔrɔ ye walasa ka den bangeli labɛn.

Ne ka kan ka ɲininkali jumɛnw kɛ n ka dɔgɔtɔrɔ la?

A bɛnnen don ka ɲininkali caman kɛ i hakili la nin waati in ɲɔgɔn na. Aw bɛ a ɲini ka nin ɲininkali ninnu kɛ aw ka dɔgɔtɔrɔ la:

• Ne den ka bana sɛgɛsɛgɛli sababu jɔnjɔn ye mun ye?
• Yala ne mago bɛ opereli la ne den bangenen kɔfɛ wa?
• Aw ye furakɛli minnu fɔ, olu kɔlɔlɔ jumɛnw bɛ yen?
• Ne den min bɛ ni Potter syndrome ye, o bangecogo jumɛn ka fisa ni tɔw bɛɛ ye?
• Ne bɛ se ka mun kɛ walasa ka ne den dɛmɛ a ka kisi?

A bɛ se ka kɛ ko ye min bɛ mɔgɔ dusu tiɲɛ kosɛbɛ ani min ka gɛlɛn ka kibaruya in kunbɛn ko a bɛ se ka kɛ ko den tɛ se ka kisi bana ma min bɛ se ka a ka ɲɛnamaya bila farati la. Aw ka dɔgɔtɔrɔ bɛna baara kɛ ɲɔgɔn fɛ ni aw ye walasa ka den ka bana sɛgɛsɛgɛli dɔn. U bɛna a lajɛ ni den tɛ a la ani ka furakɛli teliya la walasa ka bana taamasiɲɛw lajɔ a bangenen kɔfɛ.

A laban na, fɛn minnu ka kan ka to an hakili la

Potter Syndrome ye bana ye min bɛ mɔgɔ dusu tiɲɛ tiɲɛ na. Ni i y’o dɔn, i bɛ se ka dusukasi kosɛbɛ ani ka siran. O ye ko ye min tɛ kojugu ye.

• aw hakili to a la ko nin ye ko ye min man teli ka kɛ .
• O kunba ye den sugunɛw tɛ yiriwa ka ɲɛ o la denso kɔnɔji bɛ dɔgɔya .
• a dɔnni joona kɔnɔmaya waati la , o nafa ka bon .
• Ni bana taamasiɲɛw ka jugu, den caman tɛna kisi . A ka gɛlɛn kosɛbɛ ka nin dɔn, nka a nafa ka bon ka kuma o kan ni tiɲɛ ye.
• I kelen tɛ. I ka dɔgɔtɔrɔso jɛkulu, i somɔgɔw ani i teriw bɛna i dɛmɛ nin waati gɛlɛn in na . Aw kana siga ka ladili ɲini ni aw mago bɛ a la.

An jigi b’a kan ko nin kunnafoniw y’aw dɛmɛ ka faamuyali dɔ sɔrɔ nin bana in kan min man teli ka sɔrɔ. Ni ɲininkali wɛrɛw bɛ aw fɛ, aw kana siga ka kuma aw ka dɔgɔtɔrɔ fɛ.

` Potter syndrome, Potter syndrome, den, sugunɛ, kɔnɔbara basigilen, kɔnɔmaya, taamasiɲɛw, furakɛli