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🩺 Farikolo bɛ baara kɛ cogo min na

Yala nin bana in bɛ aw den na min man teli ka sɔrɔ wa? Aw ye kunnafoni sɔrɔ Cornelia de Lange Syndrome (CdLS) kan .

MBBS

Medically reviewed by MBBS — Updated on Jul 13, 2026 · 8 min read

Yala nin bana in bɛ aw den na min man teli ka sɔrɔ wa? Aw ye kunnafoni sɔrɔ Cornelia de Lange Syndrome (CdLS) kan .
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I n’a fɔ bangebaga, n’a sɔrɔ i bɛ miiri tuma bɛɛ i denmisɛnnin ka kɛnɛya n’a ka yiriwali la. Tuma dɔw la, an bɛ na ni cogoyaw ye minnu man ca kosɛbɛ, an tɛ caman mɛn minnu ko la. O jamu bana sugu dɔ min man ca nka a nafa ka bon, o ye Cornelia de Lange Syndrome ye, walima (CdLS) ni a surunyalen don. Sani an ka siran nin ko in ɲɛ, an ka kuma o kan cogo nɔgɔman na ani ka jɛya ani k’a faamu a ye min ye.

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Cornelia de Lan ka bana (CdLS) ye mun ye tigitigi?

N’an y’a fɔ cogo nɔgɔman na, (CdLS) ye jamu bana ye min man ca kosɛbɛ, min bɛ sɔrɔ bange waati. A bɛ se ka den farikolo yɔrɔ caman minɛ. Ni an b’a fɛ ka tiɲɛ fɔ, a bɛ sɔrɔ fɛn dɔ Changement (mutation) fɛ jamu damadɔw la minnu bɛ tali kɛ an farikolo yiriwali la.

O bana in bɛ se ka ye cogoba fila la. kelen ye cogoya nɔgɔman ye , tɔ kelen ye klasiki cogoya ye . A ka c’a la, ni an bɛ kuma bana in kan, an bɛ kuma klasiki suguya de kan. Nka, denmisɛnni minnu ka bana ka nɔgɔn, olu fana bɛ se ka nin taamasiɲɛ kelenw jira, nka u ka dɔgɔn.

A ka ca a la CdLS bɛ den minnu na, olu bɛ bange u girinya ni u bonya la. U kunkolo lamini fana bɛ se ka dɔgɔya ka tɛmɛ den kɛnɛman ta kan. Furakɛcogo la, o bɛ wele ko mikrosɛfali . Ka fara o farikolo caman yeli kan, hakili ni kɛwale gɛlɛya dɔw bɛ se ka sɔrɔ. Denmisɛn dɔw fana bɛ se ka kuma kɔtigɛ.

Nin bana in taamasiɲɛw ye jumɛnw ye?

CdLS taamasiɲɛw bɛ se ka ye sani den ka bange walima a bangenen kɔfɛ. Fɛn dɔw bɛ yen minnu ka teli ka kɛ denmisɛnniw yecogo la minnu bɛ nin bana in na. U bɛ se fana ka gɛlɛyaw ye dumunikɛminɛnw ni hakili yiriwali la. An ka ninnu lajɛ tabali dɔ kɔnɔ.

Jogo suguya Fɛn minnu ka kan ka ye
Farikolo jogo jɔnjɔnw
Kungolo ni ɲɛda - A ka dɔgɔn ka tɛmɛ kunkolo kan (Microcephalie) .
- Ɲɛkisɛ janw
- Ɲɛkisɛ minnu tilalen don cɛmancɛ la, minnu ka fin walima minnu ka bon
- Kunsigi duguma
- Nugu wulilen, a ka surun
- Jiginni, dawolo finmanw
- ɲinw ni ɲɛw minnu ka jan ɲɔgɔn na
Farikolo yɔrɔ wɛrɛw - Farikolo kunsigi falen kojugu
- Gɛlɛya minnu bɛ bolow ni senw yiriwali la
- Dusukun tantanni
- Dawolo tigɛlen
- Cryptorchidisme (cɛmancɛw ka cɛya minnu tɛ jigin) .
Kɔnɔnakow gɛlɛyaw
Gɛlɛya minnu bɛ sɔrɔ tuma caman na - Kɔnɔja
- Kɔnɔboli
- Fɔɔnɔ
- Kɔnɔbara fa
- Dumuni nege bɛ mɔgɔ minɛ tuma dɔw la
- Kɔnɔbara basigilen (GERD) .
Hakilila ni kɛwale gɛlɛyaw
Taamacogo ni yiriwali - Yiriwali min bɛ to kɔfɛ
- Kalanbaliya
- Taamacogo gɛlɛyaw
- Hakilila-jɔ-bana (TDAH) .
- Jɔrɔ
- Autizmu cogoyaw (Autisme)

Ka fara o kan, denmisɛn dɔw fana bɛ se ka mɛnni ni yelikɛbaliya sɔrɔ (misali la, ɲɛnamini).

Mun de bɛ o kɛ? Yala o ye ciyɛn ye wa?

CdLS ye bana ye min bɛ se ka mɔgɔ bɛɛ minɛ, siya walima cɛya mana kɛ min o min ye. A ka ca a la, a bɛ sɔrɔ jamu caman cili fɛ min bɛ kɛ a yɛrɛma, wa a ma deli ka ye denbaya kɔnɔ fɔlɔ.

Fɔlɔ, jɛnɛya 7 ɲɔgɔn Sɔrɔla minnu bɛ CdLS bana in Lase mɔgɔ ma. Nin bana in bɛ denmisɛn min na, o bɛ se ka fɛn caman Changements dans les gènes kelen walima caman. Bana suguya n’a juguya bɛ bɔ jamu caman na, jamu caman cili bɛ kɛ jamu min na ani cogo min na. Misali la, denmisɛn minnu ka jamu yeli bɛ (NIPBL) la, olu taamasiɲɛw bɛ se ka juguya ka tɛmɛ.

Min nafa ka bon, o ye ko ni den kelen bɛ denbaya kɔnɔ ni CdLS ye, den nata ka se ka a sɔrɔ, o ka dɔgɔ kosɛbɛ (1-2%).

Nka, a man teli ka kɛ, ni CdLS bana bɛ bangebaga kelen na, a bɛ se ka kɛ 50% ye ko den bɛna o ciyɛn ta. O bɛ Weele ko (Autosomal dominant) ciyɛn.

Bana in bɛ se ka sɛgɛsɛgɛ cogo di?

Ni aw bɛ sigasiga ko nin taamasiɲɛ ninnu bɛ aw den na, aw ka fɛɛrɛ fɔlɔ ka kan ka kɛ denmisɛnw ka dɔgɔtɔrɔ dɔ ye .

Dɔgɔtɔrɔ bɛna fɔlɔ ka den farikolo sɛgɛsɛgɛ ka ɲɛ, ka aw ɲininka aw den ni a ka denbaya ka furakɛli tariku la. U bɛna farikolo taamasiɲɛw ni taamasiɲɛw ɲini kɛrɛnkɛrɛnnenya la minnu bɛ tali kɛ CdLS la.

O kɔ, a bɛ se ka fɔ ko jamu sɛgɛsɛgɛli ka kɛ walasa ka bana in sɛgɛsɛgɛ. O bɛ fɛn caman ɲini fɛn caman Changements dans les gènes:

  • NIPBL
  • SMC1A ye
  • RAD21 ye
  • SMC3
  • HDAC8

Kɔnɔmaya waati, ni ultrasound scan ye dɔgɔkun 18-20 cɛ, o bɛ se ka den ɲɛda walima a senkɔniw na tuma dɔw la. O bɛ se ka taamasiyɛn dɔw di CdLS ko la.

A bɛ furakɛ cogo di?

A nafa ka bon ka nin dɔn: Furakɛli kɛrɛnkɛrɛnnen si tɛ yen min bɛ se ka CdLS furakɛ pewu. Nka, o kɔrɔ tɛ ko foyi tɛ yen an bɛ se ka min kɛ. Furakɛli kunba ye ka den ka bana taamasiɲɛw kunbɛn ani k’a dɛmɛ a ka ɲɛnamaya kɛ kɛnɛya ni nisɔndiya la.

Dɔgɔtɔrɔ kelen tɛ se ka kɛ o la. Kɛrɛnkɛrɛnnenya la ani furakɛlikɛlaw ka jɛkulu dɔ bɛ bɔ baara suguya caman na walasa ka furakɛli fɛɛrɛ ɲuman dilan den ye. Nin ekipu in bɛ se ka kɛ mɔgɔw ye i n’a fɔ:

  • Denmisɛnw ka dɔgɔtɔrɔw
  • Dusukun dɔgɔtɔrɔw - dusukunnabanaw kama
  • Farikoloɲɛnajɛla - ka farikolo lamagacogo ɲɛ ani ka farikolo fanga bonya
  • Kuma banaw dɔnbagaw - kuma ni kumaɲɔgɔnya gɛlɛyaw kama
  • Kɔnɔbaralabanaw - kɔnɔbara gɛlɛyaw kama
  • Ɲɛ kɛrɛnkɛrɛnnenw ni ENT operelikɛlaw

Tuma dɔw la, opereli bɛ se ka kɛ walasa ka dawolo walima dusukunnabana dɔ labɛn. Fura bɛ se ka di fana gɛlɛyaw ma i n’a fɔ kɔnɔbara asidi. Nin latigɛ ninnu bɛɛ bɛ kɛ dɔgɔtɔrɔw fɛ minnu bɛ aw den sɛgɛsɛgɛ.

I bɛ se ka mun fɔ siniko ko la?

N’a sɔrɔ i dusu sumana n’i y’o mɛn. CdLS bɛ denmisɛn minnu na, olu fanba bɛ ɲɛnamaya kɛ cogo la min bɛ bɛn. Nka, ikomi hakiliɲagami hakɛ dɔ bɛ u la, u mago bɛna kɛ dɛmɛ ni kɔlɔsili dɔw la u ka ɲɛnamaya bɛɛ kɔnɔ, hali fo ka se u balikuya ma. O kɔrɔ ye ka sigida lakananen di u ma walasa u ka se ka sigi ani ka baara kɛ, ka sɔrɔ ka yɛrɛmahɔrɔnya dɔ di u ma.

Nka, a man teli ka kɛ, gɛlɛya dɔw bɛ se ka mɔgɔ si hakɛ surunya. Kɛrɛnkɛrɛnnenya la, sɔgɔsɔgɔninjɛ min bɛ segin-ka-bɔ, dusukunnabana bangenenw, ani dumunikɛbaliya jugumanw, olu bɛ farati la ni a ma sɛgɛsɛgɛ ka ɲɛ.

O la, min nafa ka bon kosɛbɛ, o ye ka i den to dɔgɔtɔrɔ ka ladilikanw ni ladonni ɲumanw kɔrɔ. N’i ​​y’o kɛ, i den bɛna cogo ɲuman sɔrɔ ka ɲɛnamaya jan ni nisɔndiya la.

Take-Home cikan

  • Cornelia de Lange Syndrome (CdLS) ye bana ye min man teli ka sɔrɔ jamu fɛ, a bɛ sɔrɔ kabini a bange waati.
  • A taamasiɲɛw bɛ se ka ɲɔgɔn ta kosɛbɛ den ni den cɛ. A taamasiɲɛw bɛ se ka kɛ dɔw la, ka sɔrɔ taamasiɲɛ jugumanw bɛ se ka kɛ dɔw la.
  • Hali ni fura kɛrɛnkɛrɛnnen tɛ o la, ka bana taamasiɲɛw kunbɛn, o bɛ se ka den dɛmɛ a ka ɲɛnamaya kɛ cogo ɲuman na.
  • Dɔgɔtɔrɔw ni furakɛlikɛlaw ka kulu dɔ ka dɛmɛ nafa ka bon o la.
  • Ni siga dɔ bɛ aw den na, aw kana mɛn ka taa denmisɛnw ka dɔgɔtɔrɔ dɔ fɛ. Ni ladonni ni kanuya bɛnnen don, o denmisɛnw fana bɛ se ka ɲɛnamaya kɛ nisɔndiya la.
🔍 Search Keywords: what to know about cornelia de lange syndrome • what to know about cornelia de lange syndrome symptoms • what to know about cornelia de lange syndrome causes and treatment • what to know about cornelia de lange syndrome sri lanka • Yala nin bana in bɛ aw den na min man teli ka sɔrɔ wa? Aw ye kunnafoni sɔrɔ Cornelia de Lange Syndrome (CdLS) kan .

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