Ƙungiyar Raɗawar Haihuwa
Sashin ciwon Hydrolethalus wani ɓangare ne na cututtuka na haihuwa da cutar ta haifar. An gano cutar ciwon Hydrolethalus lokacin da masu bincike ke nazarin wani cuta, wanda ake kira Meckel, a Finland. Sun sami magungunan cutar hydrolethalus guda 56 a Finland, wanda ke nufin an samu akalla 1 cikin yara 20,000 a can. Akwai lokuta akalla 5 wasu lokuta da aka ruwaito cutar cutar hydrolethalus da aka buga a cikin wallafe-wallafe na duniya.
Yin amfani da jaririn Finnish da iyalansu, masu binciken sun gano ma'anar maye gurbin da ke da alhakin ciwo na hydrolethalus a cikin al'ummar Finnish. Ginin, wanda ake kira HYLS-1, yana kan chromosome 11. Bincike ya nuna cewa maye gurbin kwayar halitta an gaji ne a cikin wani tsari na kwance.
Symptoms of Hydrolethalus Syndrome
Hadisin Hydrolethalus ya ƙunshi rukuni na lalacewar haihuwa, wanda ya haɗa da:
- Mai tsananin hydrocephalus (wuce haddi a cikin kwakwalwa)
- Mafi ƙananan ƙananan jaw (wanda ake kira micrognathia)
- Sarewa mai laushi ko shinge
- Tsarin motsa jiki mara lafiya
- Abun ciki na zuciya
- Ƙarin yatsunsu da yatsun kafa (wanda ake kira polydactyly), musamman ma a ƙididdige babban yatsun
- Malformation na kwakwalwa, ciki har da siffofin ɓacewa
Binciken asalin Hydrolethalus Syndrome
Yawancin jarirai da ciwon hydrolethalus an gane su kafin haihuwa ta hanyar daukar matakan dan tayi. Hanyoyin hydrocephalus da kwakwalwar kwakwalwa suna bada shawara akan ganewar asali.
Binciken jaririn ta hanyar tarin dan tayi, ko jariri a lokacin haihuwa, ana buƙatar yin hukunci akan irin raunin irin su Meckel , Trisomy 13 , ko cutar Smith-Lemli-Opitz.
Outlook
Sau da yawa an haifi jaririn da ciwon hydrolethalus ba tare da daɗe ba. Kimanin kashi 70 cikin dari na jariran da ke fama da ciwo sun kasance har yanzu. Wadanda aka haife su ba su tsira ba sosai.
Sources
Tiller, George E .. "Hydrolethalus Syndrome 1." OMIM Database. 09 Jan 2007. NCBI.
Salonen, R., da R. Herva. "Hadarin Hydrolethalus." Journal of Medical Genetics 27 (1990): 756-759. Buga.