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Menene Ciwon Fraser? Bari mu yi magana game da wannan yanayin da ba kasafai ake samunsa ba

Menene Ciwon Fraser? Bari mu yi magana game da wannan yanayin da ba kasafai ake samunsa ba

Jariri jariri yana kawo farin ciki mai yawa ga iyali. Amma a lokaci guda, abu ne na al'ada a gare ku, a matsayinku na uwa ko uba, ku sami wasu tsoro da shakku. Wani lokaci, ana haihuwar yaro da wata cuta mai matuƙar wahalar ganewa wadda ba mu taɓa ji ba. Yana da wuya a faɗi abin da muke ji a irin wannan lokacin. A yau za mu yi magana game da wata cuta mai wuya, wato Fraser Syndrome.

Da farko, bari mu gani, menene wannan cutar ta kwayoyin halitta?

A taƙaice dai, duk abin da ke jikinmu kwayoyin halittarmu ne ke sarrafa shi. Abubuwa kamar launin gashinmu, launin ido, da tsayi ana tantance su ta waɗannan kwayoyin halitta. Wani lokaci, wasu canje-canje, ko maye gurbi, na iya faruwa a cikin waɗannan kwayoyin halitta. A lokacin ne cututtukan kwayoyin halitta ke faruwa. Wasu daga cikinsu ana iya ganin su a lokacin haihuwa, yayin da wasu kuma na iya bayyana daga baya.

Ciwon Fraser wani irin yanayi ne na kwayoyin halitta, wanda ba kasafai ake samunsa ba. Yana faruwa da wuri a lokacin da yaro ke girma a cikin mahaifa. Yana shafar mutane ƙalilan a duniya. Yana iya faruwa a cikin maza da mata.

Mene ne alamun yaro da ke fama da cutar Fraser?

Alamomin wannan yanayin na iya bambanta daga yaro zuwa yaro. Wannan yana nufin cewa ba kowane yaro zai nuna alamun iri ɗaya ba. Duk da haka, akwai manyan alamu da sauran alamu da ake gani akai-akai.

Abu mafi mahimmanci shine likita ya kamata ya duba yaron don gano wannan yanayin. Kada ku yi gaggawar yanke hukunci bisa ga alamun da aka ambata a nan.

Teburin da ke ƙasa yana nuna wasu daga cikin alamomin da aka fi gani a cikin wannan yanayin.

Sashen jiki Siffofin da ake iya gani
Idanu

  • Idanun ido ba sa girma yadda ya kamata ko kuma fata ta rufe su gaba ɗaya. (Wannan ana kiransa Cryptophthalmos kuma shine mafi yawan alamun cutar.)
  • Ƙananan idanu (Microphthalmia) ko kuma babu idanu (Anophthalmia).
  • Matsalolin hanyoyin tsagewa.
  • Ƙara tazara tsakanin idanu (Hypertelorism).

Hannu da Ƙafafu

  • Yatsu ko yatsun kafa da suka manne tare ( Syndactyly ).

Koda

  • Rashin koda ɗaya ko duka biyun.
  • Koda ba ta girma yadda ya kamata ko kuma ta zama ba ta da tsari.

Tsarin haihuwa (Al'aura)

  • Matsalolin da suka shafi ƙwai, fitsari, ko azzakari a cikin samari.
  • Matsalolin da suka shafi bututun mahaifa, mahaifa, ko farji a cikin 'yan mata.

Wasu fasaloli

  • Matsalolin kunne a tsakiyar kunne.
  • Rashin dubura (Anal atresia) ko kuma kunkuntar ciki (Anal stenosis).
  • Harshe mai kama da na bifid.
  • Matsalolin da ke faruwa a wurin hakora.

Baya ga waɗannan alamomin, akwai wasu alamomin da ba a saba gani ba. Idan ka lura da wani abu mai ban mamaki ko daban a jikin ɗanka, yi magana da likitanka nan da nan .

Me yasa wannan yanayin ya faru?

Kamar yadda muka tattauna a baya, wannan yanayi ne da ke faruwa sakamakon lahani a cikin kwayoyin halitta. Musamman ma, canje-canje a cikin kwayoyin halittar FRAS1, FREM2, da GRIP1 su ne manyan abubuwan da ke haifar da hakan.

Muna kiran wannan tsarin yaduwar kwayoyin halitta 'Autosomal Recessive' . Yanzu bari mu ga yadda za mu fahimci wannan a sauƙaƙe.

Ka yi tunanin cewa mahaifiyarka da mahaifinka suna da kwafin wannan kwayar halitta mai lahani a jikinsu. Amma ba su da cutar, domin suna da kwafin kwayar halitta mai lahani guda ɗaya kawai. Muna kiransu 'masu ɗauke da cutar'.

Yanzu, idan waɗannan iyaye masu ɗauke da ɗa suka haifi ɗa,

  • Akwai kashi 25% (ɗaya cikin huɗu) damar cewa yaro zai iya samun wannan yanayin (idan iyaye biyu suka gaji kwafin kwayar halittar da ke da matsala).
  • Akwai kashi 50% (ɗaya cikin biyu) damar cewa yaron zai kasance mai ɗauke da cutar da ba ta nuna alamun cutar ba, kamar iyayen.
  • Akwai kashi 25% na yiwuwar yaron ba zai gaji wannan kwayar halitta mai lahani ba kwata-kwata kuma zai kasance cikin koshin lafiya.

Wannan kamar jefa tsabar kuɗi ne. Wannan haɗarin iri ɗaya ne a kowace ciki.

Yaya ake gane wannan yanayin?

Yawanci ana gano wannan yanayin kafin a haifi jaririn, wato, a lokacin daukar ciki. Likitoci suna zargin hakan idan aka ga wani rashin lafiya a cikin koda, huhu, ko yatsun jaririn yayin gwajin duban dan tayi tsakanin makonni 18 zuwa 20. Likitoci suna ba da kulawa ta musamman ga wannan, musamman idan wani a cikin iyali ya taɓa samun wannan yanayin a baya.

Wani lokaci, idan ba a iya gano hoton ba, ana gano yanayin ne bisa ga halayen jiki da ake da su a lokacin haihuwa. Haka kuma ana iya yin gwajin kwayoyin halitta don tabbatar da ganewar cutar.

Yaya batun maganin da kuma makomar yaron?

Babu maganin cutar Fraser tukuna. Amma hakan ba yana nufin babu abin da za ku iya yi ba. Babban burin magani shine a kula da alamun yaron da kuma ba shi ingantacciyar rayuwa.

  • Tiyata: Wasu matsalolin jiki (misali, yatsun hannu da ke kan gado, idanu masu ƙyalli) za a iya gyara su ta wani mataki ta hanyar tiyata.
  • Kulawa Mai Tallafi: Wannan shine mafi mahimmanci. Yaron yana buƙatar kulawar ƙungiyar likitoci waɗanda suka ƙunshi ƙwararru daban-daban. Misali, likitan yara, likitan jijiyoyi, da likitan ido suna aiki tare don ƙirƙirar tsarin magani ga yaron.

Tsawon rayuwar yaron ya dogara ne da tsananin alamun cutar. A cikin mawuyacin hali na matsalolin numfashi ko koda , wasu yara suna cikin haɗarin mutuwa a shekarar farko ta rayuwa. Duk da haka, yawancin yara ba tare da matsaloli masu tsanani ba za su iya rayuwa ta yau da kullun .

Shawarar kwayoyin halitta tana da matuƙar muhimmanci a irin wannan yanayi. Zai iya taimaka maka ka fahimci yanayin, haɗarin da ke tattare da sauran 'yan uwa, da kuma ɗaukar ciki nan gaba. Tambayi likitanka game da wannan.

Saƙon Ɗauka Gida

  • Ciwon Fraser cuta ce da ba kasafai ake samunta ba sakamakon lahani a cikin kwayoyin halitta.
  • Babban alamun cutar sune rashin lafiya a idanu, yatsu, kodan, da kuma tsarin haihuwa.
  • Sau da yawa ana iya gano wannan a lokacin daukar hoton ultrasound a lokacin daukar ciki ko kuma lokacin haihuwa.
  • Duk da cewa ba za a iya warkar da shi gaba ɗaya ba, tiyata da kulawa mai kyau na iya magance alamun yaron da kuma inganta rayuwarsa.
  • Kula da yaro irin wannan ƙalubale ne. Yana buƙatar goyon bayan ƙungiyar ƙwararru, ƙaunar iyali, da kuma goyon bayan wasu iyaye . Ku tuna cewa ba kai kaɗai ba ne.
  • Idan kana zargin yaronka yana da wannan matsalar, kada ka firgita ka nemi shawarar likita nan take .

Ciwon Fraser, Cututtukan Halitta, Lalacewar Haihuwa, Cryptophthalmos, Syndactyly, Cututtukan Yara, Cututtuka Masu Rarrafe, Shawarwari Kan Halitta
⚠️ 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.

💬 Comments (0)

Har yanzu ba a buga sharhi ba. Ƙara bayanin ku anan a karon farko.

Ƙara sharhin ku

Da fatan za a lissafta: 3 + 5 =
Menene Ciwon Fraser? Bari mu yi magana game da wannan yanayin da ba kasafai ake samunsa ba

Menene Ciwon Fraser? Bari mu yi magana game da wannan yanayin da ba kasafai ake samunsa ba

Jariri jariri yana kawo farin ciki mai yawa ga iyali. Amma a lokaci guda, abu ne na al'ada a gare ku, a matsayinku na uwa ko uba, ku sami wasu tsoro da shakku. Wani lokaci, ana haihuwar yaro da wata cuta mai matuƙar wahalar ganewa wadda ba mu taɓa ji ba. Yana da wuya a faɗi abin da muke ji a irin wannan lokacin. A yau za mu yi magana game da wata cuta mai wuya, wato Fraser Syndrome.

Da farko, bari mu gani, menene wannan cutar ta kwayoyin halitta?

A taƙaice dai, duk abin da ke jikinmu kwayoyin halittarmu ne ke sarrafa shi. Abubuwa kamar launin gashinmu, launin ido, da tsayi ana tantance su ta waɗannan kwayoyin halitta. Wani lokaci, wasu canje-canje, ko maye gurbi, na iya faruwa a cikin waɗannan kwayoyin halitta. A lokacin ne cututtukan kwayoyin halitta ke faruwa. Wasu daga cikinsu ana iya ganin su a lokacin haihuwa, yayin da wasu kuma na iya bayyana daga baya.

Ciwon Fraser wani irin yanayi ne na kwayoyin halitta, wanda ba kasafai ake samunsa ba. Yana faruwa da wuri a lokacin da yaro ke girma a cikin mahaifa. Yana shafar mutane ƙalilan a duniya. Yana iya faruwa a cikin maza da mata.

Mene ne alamun yaro da ke fama da cutar Fraser?

Alamomin wannan yanayin na iya bambanta daga yaro zuwa yaro. Wannan yana nufin cewa ba kowane yaro zai nuna alamun iri ɗaya ba. Duk da haka, akwai manyan alamu da sauran alamu da ake gani akai-akai.

Abu mafi mahimmanci shine likita ya kamata ya duba yaron don gano wannan yanayin. Kada ku yi gaggawar yanke hukunci bisa ga alamun da aka ambata a nan.

Teburin da ke ƙasa yana nuna wasu daga cikin alamomin da aka fi gani a cikin wannan yanayin.

Sashen jiki Siffofin da ake iya gani
Idanu

  • Idanun ido ba sa girma yadda ya kamata ko kuma fata ta rufe su gaba ɗaya. (Wannan ana kiransa Cryptophthalmos kuma shine mafi yawan alamun cutar.)
  • Ƙananan idanu (Microphthalmia) ko kuma babu idanu (Anophthalmia).
  • Matsalolin hanyoyin tsagewa.
  • Ƙara tazara tsakanin idanu (Hypertelorism).

Hannu da Ƙafafu

  • Yatsu ko yatsun kafa da suka manne tare ( Syndactyly ).

Koda

  • Rashin koda ɗaya ko duka biyun.
  • Koda ba ta girma yadda ya kamata ko kuma ta zama ba ta da tsari.

Tsarin haihuwa (Al'aura)

  • Matsalolin da suka shafi ƙwai, fitsari, ko azzakari a cikin samari.
  • Matsalolin da suka shafi bututun mahaifa, mahaifa, ko farji a cikin 'yan mata.

Wasu fasaloli

  • Matsalolin kunne a tsakiyar kunne.
  • Rashin dubura (Anal atresia) ko kuma kunkuntar ciki (Anal stenosis).
  • Harshe mai kama da na bifid.
  • Matsalolin da ke faruwa a wurin hakora.

Baya ga waɗannan alamomin, akwai wasu alamomin da ba a saba gani ba. Idan ka lura da wani abu mai ban mamaki ko daban a jikin ɗanka, yi magana da likitanka nan da nan .

Me yasa wannan yanayin ya faru?

Kamar yadda muka tattauna a baya, wannan yanayi ne da ke faruwa sakamakon lahani a cikin kwayoyin halitta. Musamman ma, canje-canje a cikin kwayoyin halittar FRAS1, FREM2, da GRIP1 su ne manyan abubuwan da ke haifar da hakan.

Muna kiran wannan tsarin yaduwar kwayoyin halitta 'Autosomal Recessive' . Yanzu bari mu ga yadda za mu fahimci wannan a sauƙaƙe.

Ka yi tunanin cewa mahaifiyarka da mahaifinka suna da kwafin wannan kwayar halitta mai lahani a jikinsu. Amma ba su da cutar, domin suna da kwafin kwayar halitta mai lahani guda ɗaya kawai. Muna kiransu 'masu ɗauke da cutar'.

Yanzu, idan waɗannan iyaye masu ɗauke da ɗa suka haifi ɗa,

  • Akwai kashi 25% (ɗaya cikin huɗu) damar cewa yaro zai iya samun wannan yanayin (idan iyaye biyu suka gaji kwafin kwayar halittar da ke da matsala).
  • Akwai kashi 50% (ɗaya cikin biyu) damar cewa yaron zai kasance mai ɗauke da cutar da ba ta nuna alamun cutar ba, kamar iyayen.
  • Akwai kashi 25% na yiwuwar yaron ba zai gaji wannan kwayar halitta mai lahani ba kwata-kwata kuma zai kasance cikin koshin lafiya.

Wannan kamar jefa tsabar kuɗi ne. Wannan haɗarin iri ɗaya ne a kowace ciki.

Yaya ake gane wannan yanayin?

Yawanci ana gano wannan yanayin kafin a haifi jaririn, wato, a lokacin daukar ciki. Likitoci suna zargin hakan idan aka ga wani rashin lafiya a cikin koda, huhu, ko yatsun jaririn yayin gwajin duban dan tayi tsakanin makonni 18 zuwa 20. Likitoci suna ba da kulawa ta musamman ga wannan, musamman idan wani a cikin iyali ya taɓa samun wannan yanayin a baya.

Wani lokaci, idan ba a iya gano hoton ba, ana gano yanayin ne bisa ga halayen jiki da ake da su a lokacin haihuwa. Haka kuma ana iya yin gwajin kwayoyin halitta don tabbatar da ganewar cutar.

Yaya batun maganin da kuma makomar yaron?

Babu maganin cutar Fraser tukuna. Amma hakan ba yana nufin babu abin da za ku iya yi ba. Babban burin magani shine a kula da alamun yaron da kuma ba shi ingantacciyar rayuwa.

  • Tiyata: Wasu matsalolin jiki (misali, yatsun hannu da ke kan gado, idanu masu ƙyalli) za a iya gyara su ta wani mataki ta hanyar tiyata.
  • Kulawa Mai Tallafi: Wannan shine mafi mahimmanci. Yaron yana buƙatar kulawar ƙungiyar likitoci waɗanda suka ƙunshi ƙwararru daban-daban. Misali, likitan yara, likitan jijiyoyi, da likitan ido suna aiki tare don ƙirƙirar tsarin magani ga yaron.

Tsawon rayuwar yaron ya dogara ne da tsananin alamun cutar. A cikin mawuyacin hali na matsalolin numfashi ko koda , wasu yara suna cikin haɗarin mutuwa a shekarar farko ta rayuwa. Duk da haka, yawancin yara ba tare da matsaloli masu tsanani ba za su iya rayuwa ta yau da kullun .

Shawarar kwayoyin halitta tana da matuƙar muhimmanci a irin wannan yanayi. Zai iya taimaka maka ka fahimci yanayin, haɗarin da ke tattare da sauran 'yan uwa, da kuma ɗaukar ciki nan gaba. Tambayi likitanka game da wannan.

Saƙon Ɗauka Gida

  • Ciwon Fraser cuta ce da ba kasafai ake samunta ba sakamakon lahani a cikin kwayoyin halitta.
  • Babban alamun cutar sune rashin lafiya a idanu, yatsu, kodan, da kuma tsarin haihuwa.
  • Sau da yawa ana iya gano wannan a lokacin daukar hoton ultrasound a lokacin daukar ciki ko kuma lokacin haihuwa.
  • Duk da cewa ba za a iya warkar da shi gaba ɗaya ba, tiyata da kulawa mai kyau na iya magance alamun yaron da kuma inganta rayuwarsa.
  • Kula da yaro irin wannan ƙalubale ne. Yana buƙatar goyon bayan ƙungiyar ƙwararru, ƙaunar iyali, da kuma goyon bayan wasu iyaye . Ku tuna cewa ba kai kaɗai ba ne.
  • Idan kana zargin yaronka yana da wannan matsalar, kada ka firgita ka nemi shawarar likita nan take .

Ciwon Fraser, Cututtukan Halitta, Lalacewar Haihuwa, Cryptophthalmos, Syndactyly, Cututtukan Yara, Cututtuka Masu Rarrafe, Shawarwari Kan Halitta
⚠️ 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.

💬 Comments (0)

Har yanzu ba a buga sharhi ba. Ƙara bayanin ku anan a karon farko.

Ƙara sharhin ku

Da fatan za a lissafta: 3 + 5 =