Yu pikin in kidni nɔ de wok fayn? Lɛ wi no bɔt dis Pɔta Sindrom!

If yu na mama we go bi mama, yu go mɔs de wɔri bɔku bɔt yu pikin in wɛlbɔdi, nɔto so? I nɔmal fɔ wɔnda if yu pikin de gro fayn fayn wan na di bɛlɛ ɛn if ɔltin de go fayn. Tide wi go tɔk bɔt wan sik we nɔ kin apin so ɔltɛm we kin afɛkt pikin dɛn. Dɛn kɔl am Pɔta Sindrom. Yu kin wɔri we yu yɛri dis, bɔt i rili impɔtant fɔ no bɔt am.

Fɔ tɔk am simpul wan, wetin na Pɔta Sindrom?

Okay, mek wi brok am dɔŋ. Potter syndrome, we sɔm pipul dɛn kin kɔl di Potter sequence , na wan sik we nɔ kin apin so ɔltɛm we kin afɛkt di pikin in divɛlɔpmɛnt we dɛn de na di bɛlɛ. di men tin we kin mek dis apin na dat di pikin in kidni dεm nכ de divεlכp fayn כ dεn nכ de wok fayn . yu no se we pikin de na di bεlε, bכku amniotic fluid de rawnd dεm. di kidni dεm de ple big rol fכ kip di amoun fכ dis amniotic fluid in chεk. so we di kidni dεm nכ de wok fayn, di כmכnt fכ dis amniotic fluid de dכn. Dis na wetin dɔktɔ dɛn kin kɔl oligohydramnios.

i sɔri fɔ no se sɔm tɛm dɛn kin bɔn pikin we nɔ gɛt ɔl tu di kidni dɛn, we na wan sik we dɛn kɔl ``Bilateral Renal Agenesis``, we kin kil pɔsin. Bɔt sɔm pikin dɛn kin liv if dɛn sik nɔ kin bɔku ɔ if di wata we dɛn kin lɔs nɔ kin rili bad. Bɔt dɛn pikin ya kin gɛt prɔblɛm wit dɛn lɔng ɛn kidni we nɔ de dɔn as dɛn de ol.

Udat dɛn go mɔs afɛkt dis kayn tin?

Fɔ tru, dis sik we dɛn kɔl Potter syndrome kin afɛkt ɛni pikin. Bikɔs i gɛt fɔ du wit di sik we dɛn kɔl amniotic fluid we nɔ bɔku. Bɔt sɔm stɔdi dɛn dɔn sho se man pikin dɛn kin gɛt dis sik smɔl .

Yu tink se pɔsin we gɛt di sik we dɛn kɔl Potter syndrome?

Dis na tin we kɔmplikt smɔl. Potter syndrome nɔto wan sik we pɔsin kin gɛt frɔm in jɛnɛtiks. Bɔt sɔm tin dɛn de we kin mek i gɛt am. Lɛ wi tek wan luk pan wetin dɛn bi:

• Polisistik kidni sik: dis kin kכmכt frכm di mama כ di papa (autosomal dominant) כ frכm di tu mama εn papa (autosomal recessive). dis kin mek sist dεm fכm na di kidni dεm.
• di rεnal agenesis: Dis na di fεil we di kidni dεm de fεl fכ divεlכp. sכmtεm dis kin bi fכ di mכtεshכn dεm na di jin dεm FGF20 כ GREB1L. dis kכndishכn kin inhεrit insay כtosom dכminant כ כtosom rεsεsiv we. Dis min se di pikin fɔ gɛt di muteshon frɔm wan pan in mama ɔ papa ɔ ɔl tu in mama ɛn papa.
• Wan wan tɛm na di jɛnɛtik chenj: Sɔntɛnde, wan random jenɛtik chenj kin mek pɔsin gɛt Pɔta sindrom, ivin if nɔbɔdi na di famili nɔ bin dɔn gɛt dis sik bifo.

Aw dis sik kin kɔmɔn?

Potter syndrome na wan sik we nɔ kin apin so ɔltɛm . Dɛn se dis sik kin afɛkt wan pan ɛvri 4,000 to 10,000 pikin dɛn we dɛn bɔn. So nɔ fred we yu yɛri bɔt am. Bɔt i impɔtant fɔ mek wi no.

Aw di sik we dɛn kɔl Potter syndrome kin afɛkt pikin in bɔdi?

Dis na di tin we impɔtant pas ɔl. Pɔta sindrom kin afɛkt di we aw di pikin in insay pat dɛn, mɔ di kidni dɛn, de divɛlɔp ɛn wok . As yu no, di kidni na impɔtant ɔgan dɛn we de pul dɔti tin dɛn ɛn ɛkstra wata na wi bɔdi. we di pikin de insay di bεlε, di kidni dεm de mek urine. dis urine de risaykul as amniotic fluid.

so, if di pikin in kidni dεm nכ de wok fayn, dεn nכ go prodyuz inof amniotic fluid fכ rawnd dεm. dis amniotic fluid na in de kush di pikin. we dis wata dכn lכs, di we aw di pikin in כgan dεm εn in bכdi de divεlכp de afekt. In ɔda wɔd dɛn, di ɔgan dɛn nɔ de divɛlɔp ful wan . Dɔn dɛn ɔgan dɛn de nɔ kin ebul fɔ du dɛn wok fayn fayn wan. Dis na wae kin mek yu gɛt sayn dɛm wae kin mek yu layf de pan denja.

Wetin na di sayn dɛm wae de sho se pɔrsin gɛt pɔta sik?

Di sayn dɛm fɔ Potter syndrome kin difrɛn frɔm wan pikin to ɔda pikin, ɛn aw di sik kin tranga kin difrɛn. Dɛn sayn ya kin afɛkt yu bɛlɛ bak, we kin mek yu bɔn pikin bifo tɛm .

Lak fɔ amniotic fluid

we di pikin bεlε, wan klia, yכlכsh wata de rawnd di pikin. Dis na di amniotic fluid. Dis kin protɛkt di pikin ɛn gi am ples fɔ gro. i de wok lεk barεri bitwin di uterin wכl εn di pikin. di pikin dεm we gεt Pכta sεndrכm nכ gεt inof fכ dis amniotic fluid, so di prεshכn we de kכmכt na di uterin wכl de afekt di we aw di pikin de gro.

Speshal tin dɛn we de na di fes ɛn bɔdi

di prεshכn we di pikin in bכdi nכ de kכmכt de afekt di we aw di pikin in bכdi de divεlכp. Dis kin mek sɔm patikyula tin dɛn na in fes. Dɛn kɔl dis "Potter facies" . Dɛn tin ya na:

• di chin nכ de divεlכp fayn (i tan lεk se dεn tכn am insay).
• Fɔ gɛt wrinkle dɔŋ di lip we de dɔŋ.
• Dɛn put di yay dɛn fa fawe.
• Di brij we bin de na Naha bin flat.
• di yes dεm we dεn sכt lכw εn di kכtilaj dεm we de dכn na di yes dεm.
• Skin de fold na di kɔna dɛn na di yay.

dis prεshכn kin afekt bak di divεlכpmεnt fכ כda pat dεm na di pikin in bכdi. Fɔ ɛgzampul:

• Di an ɛn leg dɛn we shɔt.
• we yu nכ ebul fכ εksεnd εn strεt di joyn dεm fayn fayn wan, εn stiffness (kכntrakt).
• di pikin in saiz smɔl we yu kɔmpia am wit di ej we i gɛt bɛlɛ.

Ɔgan dɛn we nɔ de divɛlɔp ɔ we nɔ fayn

Di sayn dɛm wae de afɛkt di ɔgan dɛm na dɛn kin de pan denja pas ɔl.. insay Potter syndrome, di pikin in divεlכpmεnt de afekt, so di insay כgan dεm nכ de gεt di instrכkshכn כ tεm we dεn nid fכ divεlכp fayn fayn wan. Di sayn dɛm wae kin apun as a rizulta na:

• Di at kɔndishɔn dɛn we dɛn bɔn wit.
• Ay sik dεm (e.g. katarakt, lεns lכkshכn).
• Kidni sik dεm (krכnik kidni fεil, kidni agenesis, polycystic kidni sik).
• Lכng sik dεm (krεse lכng sik, rεspiretכri distres).

di kidni divεlכpmεnt we nכ nכmal de afekt bak di כmכnt כf urine we nyu bכbi kin prodyuz. Dis na sayn bak we dɔktɔ dɛn kin luk fɔ we dɛn de no se pɔsin gɛt Pɔta sindrom.

Wetin na di tin dɛn we kin mek pɔsin gɛt pɔta sik?

Bɔku tin dɛn de we kin mek pɔsin gɛt di sik we dɛn kɔl Potter syndrome. Dɛn na:

• Kidni we nɔ de divɛlɔp fayn ɔ we nɔ gɛt ɛni kidni.
• Polisistik kidni sik.
• Prune bɛlɛ sindrom (Prune bɛlɛ sindrom / Eagle-Barrett sindrom) .
• Blɔk na di urinary tract.
• Lik fכ di amniotic fluid bikoz fכ di rכpchכ fכ di mεmbran dεm.
• Di mεdikal kכndyushכn dεm we dεn nכ kin kכntrol na di mama, fכ egzampl, tayp 1 dayabεtis.

dis simptom dεm, spεshal wan dεm we de afekt di kidni dεm, kin apin bi כs nכ inof amniotic fluid de na di bεlε fכ rawnd di pikin .

Wetin mek dis amniotic fluid de dכn?

Lɛ wi luk dis smɔl mɔ. Di men tin we kin mek i apin na di kidni dɛn we nɔ de gro fayn .

yu no se we yu bεlε, yu pikin de fכt insay wan klia, yכlכ wata we dεn kכl amniotic fluid. Dis wata de protɛkt yu pikin ɛn ɛp am fɔ gro ɔl di tɛm we yu gɛt bɛlɛ? di ali we yu bεlε, dis amniotic fluid na wata εn nyutriεnt dεm we de kכmכt na yu bכdi. yu pikin de drink dis amniotic fluid. bitwin wik 16 εn 20, yu pikin kin bigin fכ kכntribyut to dis amniotic fluid. Aw yu no? Na bay we yu de pis! Yu pikin de drink dis wata ɛn afta dat i de pas am as urine. Dis kin apin insay wan saykl.

So, if yu pikin gɛt Pɔta sindrom, in ɔgan dɛn we de mek urine, we na di kidni, nɔ de divɛlɔp fayn, ɔ i nɔ de, ɔ i nɔ de wok. biכs di pikin nכ kin ebul fכ pis, i nכ kin kכntribyut to di amount of amniotic fluid we de protεkt am. na dat mek di amniotic fluid de sכmtεm na di bεlε.

Difrɛn kayn pɔta sik de?

Yɛs, dɔktɔ dɛn kin difrɛns difrɛn kayn pɔta sik, i kin dipen pan di sayn dɛn we kin afɛkt di kidni dɛn.

• Klasik Pɔta sindrom: Dis na di kayn we we dɛn kin gɛt mɔ. I kin apin we dɛn bɔn pikin we nɔ gɛt ɔl tu di kidni dɛn.
• Pɔta sindrom tayp I: .dis kayn kכndyushכn de kכz fכ wan kכndyushכn we dεn kכl polycystic kidney disease, we dεn kin gεt frכm dεn tu mama εn papa εn na כtosomal rεsεsiv kכndyushכn. insay dis kכndishכn, sist dεm de fכm na di kidni dεm.
• Potter syndrome type II: Dis kayn sindrom de kכz fכ abnכmal tin dεm na di kidni divεlכpmεnt we de apin na di bεlε we uman bεlε.
• Potter syndrome type III: Dis kin kam bak bay polycystic kidney disease, lεk tayp I. כltu, i kin kכmכt frכm wan mama εn papa nכmכ (Autosomal dominant).
• Potter syndrome type IV: Dis kayn sεndrכm de kכz fכ wan obstrכkshכn na di urinary tract (obstructive uropathy) bikoz fכ di pikin in bכdi we nכ de gro fayn fayn wan.

Aw dɛn kin no se pɔsin gɛt di sik we dɛn kɔl Potter syndrome?

Dɛn kin no se pɔsin gɛt pɔta sik we uman gɛt bɛlɛ tru ɛgzam bifo dɛn bɔn am . Wan sayn we de sho se yu kin gɛt dis sik we yu gɛt bɛlɛ na we yu nɔ gɛt amniotic fluid rawnd di pikin. Yu dɔktɔ go luk fɔ dis we dɛn de du ɔltra saund skan. Dɛn go luk bak fɔ di bɔdi simptom dɛm lɛk we di jɔyn dɛn stif (kɔntrakt).

If dɛn nɔ no dis bifo dɛn bɔn di pikin, di dɔktɔ go du in bɔdi ɛgzam afta dɛn bɔn di pikin fɔ chɛk fɔ si if i gɛt di sik. Dɛn sayn ya na:

• Rili low urine output.
• Fɔ gɛt patikyula tin dɛn we yu de du na yu fes.
• I nɔ kin izi fɔ yu fɔ blo.

Us tɛst dɛn kin du fɔ kɔnfirm dis?

Di dɔktɔ kin du bɔku tɛst fɔ no if pɔsin gɛt di sik:

• Jɛnɛtik blɔd tɛst fɔ no di jin we ripɔtabl fɔ di simptom dɛm.
• Chek yu pikin in lɔng, kidni, ɛn urinary tract wit imej tɛst lɛk ɛkstrem rayt, MRI, ɔ ɔltra saund .
• Blɔd ɔ urine tɛst fɔ chɛk di ilɛktrɔlayt ɛn ɛnzaym lɛvɛl.
• Wan ɛkokardiogram tɛst fɔ chɛk fɔ si if yu gɛt sayn dɛn fɔ gɛt at sik.

Wetin na di tritmɛnt dɛm fɔ dis?

Di tritmɛnt fɔ Pɔta sindrom de dipen pan aw di lɔng ɛn at kɔmplikeshɔn (pulmonary hypoplasia) de afɛkt yu pikin, ɛn bak di opshɔn dɛm we de fɔ sɔpɔt yu pikin in kidni fɔ wok.

Tink bɔt am, yu pikin we de gro nid fɔ de rawnd amniotic fluid ɔlsay na di bɛlɛ fɔ mek in lɔng dɛn go bifo fayn fayn wan. If di pikin in chɛst ful-ɔp fɔ lɔng tɛm, i kin lɔs inof lɔng tisu fɔ liv afta dɛn bɔn am.

Fɔ trit nyu bɔbɔ we gɛt kɔmplit kidni fayl kin rili tranga. Sɔntɛnde, di intavɛnshɔn dɛn we dɛn kin du fɔ kia fɔ di pikin dɛn nɔ kin bɔku ɛn dɛn kin yuz di kia we dɛn kin kia fɔ di pikin we dɛn jɔs bɔn fɔ mek di pikin ɛn in mama ɛn papa kam togɛda ɛn fɔ mek di pikin fil fayn.Di tritmɛnt we dɛn kin du kin bi wan opshɔn.

If yu pikin de liv afta dɛn bɔn am, di tritmɛnt go mɔs pe atɛnshɔn fɔ mek i nɔ gɛt di sik dɛn we go mek i day. Dɛn tritmɛnt ya kin bi:

• Yuz di ikwipmɛnt fɔ sɔpɔt di brith (e.g. ventilator ).
• Sɔpɔt drɔgs we de ɛp fɔ mek di lɔng dɛn wok.
• Ɔpreshɔn fɔ mek ɔ pul di tin dɛn we dɔn blok na di urinary tract.
• Ɔpreshɔn fɔ mek di it bɛtɛ tru IV nyutrishɔn tɛrapi, nasogastric tyub, ɔ fidin tyub.
• Dayalaysis na tritmɛnt fɔ pul di pɔyzin we kin gɛda na di blɔd bikɔs ɔf di kidni abnɔmaliti. If di tritmɛnt fɔ dayalaysis nɔ wok afta sɔm ia, di dɔktɔ kin tɛl yu fɔ transplant yu kidni .

Dipen pan ustɛm dɛn no se yu pikin gɛt di sik, di tritmɛnt kin bigin we yu gɛt bɛlɛ. Yu kin fit bak fɔ gɛt tritmɛnt we dɛn kin du fɔ chɛk, lɛk amnioinfusion, we kin ad wata to yu amniotic cavity fɔ tek di wata we de rawnd yu pikin in ples. dis tritmεnt de wok bεst bifo 22 wiks we di bεlε de.

Yu tink se dɛn go ebul fɔ protɛkt di sik we dɛn kɔl Potter syndrome?

Bɔt i sɔri fɔ no se no we nɔ de fɔ mek pɔsin nɔ gɛt di sik we dɛn kɔl Potter syndrome .

Wetin a fɔ ɛkspɛkt if mi pikin gɛt Pɔta sindrom?

No mɛrɛsin nɔ de fɔ mɛn pɔsin we gɛt di sik we dɛn kɔl Potter syndrome. Bɔrku tɛm, if dɛn no di sik kwik kwik wan we yu gɛt bɛlɛ, yu dɔktɔ kin plan fɔ bɔn pikin fayn fayn wan ɛn gi yu tritmɛnt fɔ ɛp yu pikin fɔ liv afta dɛn bɔn am.

Di sayn dɛm wae de sho se pɔrsin gɛt pɔta sik kin mek pɔrsin in layf de pan denja. Bɔt pas yu pikin in lɔng ɛn kidni dɛn rili afɛkt di sayn dɛm, yu pikin kin gɛt bɛtɛ prɔgnosis smɔl.

Bikɔs di tritmɛnt kin bigin jɔs afta dɛn bɔn am, nɔto ɔl di tritmɛnt dɛn kin wok fayn. Sɔntɛm dɛn kin gɛt fɔ du bɔku ɔpreshɔn dɛn we dɛn smɔl.

Wetin na di layf we pikin we gɛt Pɔta sik kin liv?

Bebi dɛn we dɛn no se gɛt Pɔta sindrom kin liv shɔt layf . Dis kin difrɛn fɔ ɔlman, ɛn i kin dipen pan de sayn dɛm. If di sayn dɛm bad bad wan, ɛn if di divɛlɔpmɛnt ɛn wok we di men ɔgan dɛm lɛk di at, di lɔng, ɛn di kidni dɛn afɛkt, di prɔgnosis nɔr fayn. Bɔku pan di pikin dɛn nɔ kin liv di fɔs de dɛn we dɛn de liv . Na say dɛn we nɔ kin at fɔ si, usay di sayn dɛn nɔ kin so bad ɛn di ɔgan dɛn nɔ kin afɛkt bɔku, di layf we pɔsin kin liv kin lɔng smɔl.

Yu dɔktɔ go tɔk to yu bɔt di prɔblɛm dɛn we kin apin we dɛn no se yu pikin gɛt di sik, ɛn i go tɛl yu bɔt tritmɛnt dɛn fɔ mek i liv lɔng. If di sik we yu pikin gɛt siriɔs, di kia we yu de kia fɔ yu pikin kin bi wan we fɔ ɛp yu fɔ bia wit di pwɛl at we pɔsin kin fil we pɔsin day.Dɛn kin advays bak fɔ advays pɔsin we gɛt pwɛl hat ɔ we pɔsin day.

Ustɛm a fɔ go to dɔktɔ?

If yu notis ɛni chenj we yu gɛt bɛlɛ, mɔ if yu pikin stɔp fɔ muf wantɛm wantɛm afta i dɔn muf fayn , go to yu dɔktɔ wantɛm wantɛm. Yu pikin kin bɔn bifo tɛm pas aw yu bin de tink. So, i rili impɔtant fɔ mek yu du ɛgzam bifo yu bɔn ɔltɛm wit yu dɔktɔ fɔ rɛdi fɔ bɔn yu pikin.

Us kwɛstyɔn dɛn a fɔ aks mi dɔktɔ?

Na nɔmal tin fɔ gɛt bɔku kwɛstyɔn dɛn na yu maynd pan tɛm lɛk dis. Tray fɔ aks yu dɔktɔ dɛn kwɛstyɔn ya:

• Wetin na di men tin we mek dɛn no se mi pikin gɛt di sik?
• A go nid ɔpreshɔn afta dɛn bɔn mi pikin?
• Wetin na di sayd ɛfɛkt dɛm fɔ di tritmɛnt dɛm wae yu bin rεkomεnd?
• Wetin na di we we sef fɔ bɔn mi pikin we gɛt Pɔta sindrom?
• Wetin a go du fɔ ɛp mi pikin fɔ liv?

E kin bi wan tin wae de mek yu fil bad ɛn nɔr kin izi fɔ dil wit de nyus wae yu pikin nɔr kin sev we dɛn no se yu gɛt dis sik we go mek yu in layf de pan denja. Yu dɔktɔ go wok wit yu fɔ no aw yu pikin gɛt di sik. Dɛn go mek shɔ se yu pikin sef ɛn dɛn go gɛt tritmɛnt kwik kwik wan fɔ mek i nɔ gɛt di sik afta dɛn bɔn am.

Fɔ dɔn, tin dɛn we wi fɔ mɛmba

Potter Syndrome na wan sik we rili de mek pɔsin in at pwɛl. We yu lan bɔt am, yu go fil bad ɛn fred. Dat na nɔmal tin.

• Mɛmba se dis na tin we nɔ kin apin so ɔltɛm .
• di men rizin fכ dis na biכs di pikin in kidni dεm nכ de divεlכp fayn εn dat mek di amniotic fluid de dכn .
• Fɔ no am kwik kwik wan we uman gɛt bɛlɛ impɔtant .
• If di sik bad bad wan, bɔku pikin dɛn nɔ go liv . I rili at fɔ no dis, bɔt i impɔtant fɔ tɔk bɔt am ɔnɛs wan.
• Nɔto yu wan de. Yu mɛdikal tim, yu fambul, ɛn padi dɛn go sɔpɔt yu insay dis tranga tɛm . Nɔ shem fɔ go to advays if nid de.

Wi op se dis infɔmeshɔn dɔn ɛp yu fɔ ɔndastand sɔm kayn tin bɔt dis sik wae nɔr kin bɔrku. If yu gɛt ɛni ɔda kwɛstyɔn, nɔ shem fɔ tɔk to yu dɔktɔ.

` Potter syndrome, Potter syndrome, pikin, kidni, amniotic fluid, bɛlɛ, di simptom dɛm, tritmɛnt