Schinzel-Giedion ciwo
Wadatacce
Schinzel-Giedion Syndrome cuta ce mai saurin yaduwa a cikin haihuwa wanda ke haifar da bayyanar rashin nakasa a cikin kwarangwal, canje-canje a fuska, toshewar hanyoyin fitsari da kuma jinkirin ci gaba mai girma a cikin jariri.
Kullum, Schinzel-Giedion Syndrome ba gado bane kuma, sabili da haka, na iya bayyana a cikin iyalai ba tare da tarihin cutar ba.
NA Cutar Schinzel-Giedion ba ta da magani, amma ana iya yin aikin tiyata don gyara wasu nakasawa da inganta rayuwar jariri, duk da haka, shekarun rayuwa ba su da yawa.
Kwayar cutar Schinzel-Giedion Syndrome
Kwayar cututtukan cututtukan Schinzel-Giedion Syndrome sun haɗa da:
- Kunkuntar fuska tare da babban goshi;
- Baki da harshe sun fi girma girma;
- Yawan gashin jiki;
- Matsalolin jijiyoyin jiki, kamar rashin gani, kamuwa ko kurumta;
- Canje-canje masu tsanani a cikin zuciya, koda ko al'aura.
Wadannan alamun ana gano su ba da daɗewa ba bayan haihuwa kuma, sabili da haka, ana iya buƙatar jariri a asibiti don kula da alamun kafin a sallame shi daga asibitin haihuwa.
Baya ga alamomin alamomin cutar, jariran da ke fama da cutar Schinzel-Giedion suma suna da ci gaba da lalacewar jijiyoyin jiki, haɗarin ƙari da cututtukan da suka shafi numfashi, kamar su ciwon huhu.
Yadda za a magance cututtukan Schinzel-Giedion
Babu takamaiman magani don warkar da cutar Schinzel-Giedion Syndrome, amma, wasu jiyya, musamman aikin tiyata, ana iya amfani da su don gyara nakasawar da cutar ta haifar, yana inganta rayuwar jaririn.