Gulu Lowonongeka la Zofooka za Kubadwa
Matenda a Hydrolethlus ndi matenda obadwa obadwa chifukwa cha matenda a chibadwa. Matenda a Hydrolethalus anatulukira pamene ofufuza anali kuphunzira matenda ena, omwe amatchedwa matenda a Meckel, ku Finland. Iwo anapeza milandu 56 ya hydrolethalus syndrome ku Finland, kutanthauza kuti pafupifupi ana 1,000 aliwonse kumeneko. Panalipo ena osachepera asanu omwe analembedwapo a hydrolethalus syndrome omwe amafalitsidwa m'mabuku a zachipatala padziko lonse.
Akatswiriwa anapeza kuti ana a ku Finnish ndi mabanja awo anapeza kuti chibadwa cha mtundu wa hydrothelus syndrome chimachititsa anthu ambiri ku Finland. Geni , yotchedwa HYLS-1, ili pa chromosome 11. Kafukufuku amasonyeza kuti kusintha kwa chibadwa kumatengera mwambo wa autosomal.
Zizindikiro za Matenda a Hydrolethalus
Matenda a Hydrolethlus ali ndi kagulu ka zilema zoberekera, kuphatikizapo:
- Kutentha kwa hydrocephalus (madzi owonjezera mu ubongo)
- Mng'alu waung'ono kwambiri (wotchedwa micrognathia)
- Kuthyola pakamwa kapena phala
- Ndondomeko yopuma yopuma
- Congenital mtima zopweteka
- Zina zala zala ndi zala zazing'ono (zotchedwa polydactyly), makamaka zala zala zazikulu
- Kusokoneza ubongo, kuphatikizapo zosowa
Kuzindikira Matenda a Hydrolethalus
Ana ambiri okhala ndi hydrolethalus syndrome amazindikiridwa asanabadwe ndi ultrasound yobereka. The hydrocephalus ndi ubongo malformation amasonyeza matenda.
Pewani kuyang'anitsitsa kamwana ka ultrasound, kapena mwanayo atabadwa, nkofunika kuti mutulutse syndrome monga Meckel syndrome , Trisomy 13 , kapena matenda a Smith-Lemli-Opitz.
Chiwonetsero
Kawirikawiri mwana amene ali ndi hydrolethalus syndrome amabadwa msinkhu. Pafupifupi ana makumi asanu ndi awiri (70%) omwe ali ndi matenda ali obadwa. Anthu obadwa amoyo sakhala ndi moyo kwa nthawi yayitali.
Zotsatira
Willer, George E .. "Hydrolethalus Syndrome 1." OMIM Database. 09 Jan 2007. NCBI.
Salonen, R., & R. Herva. "Hydrolethalus syndrome." Journal of Medical Genetics 27 (1990): 756-759. Sindikizani.