Trisomy 18 iyo Edwards Syndrome

Chromosome-kani wuxuu saameynayaa Dhammaan Goobaha Jirka

Koromosoomyada bani-aadamka ayaa soo galaya 23 laba-labo, waalid walbana wuxuu halmariyaa hal kromosoom. Trisomy 18 (oo sidoo kale loo yaqaanno Edwards syndrome) waa xaalad hiddaha oo ah hal kromosome (kromosome 18) waa saddex laab halkii laba qof. Sida Trisomy 21 ( Down syndrome ), Trisomy 18 wuxuu saameeyaa dhammaan nidaamyada jidhka wuxuuna keenaa muuqaalada kala duwan.

Trisomy 18 waxay ku dhacdaa 1 qof 6,000 oo dhalasho nool.

Nasiib daro, carruurta badankood ee Trisomy 18 waxay u dhintaan dhalashada ka hor, sidaas darteed dhacdooyinka dhabta ah ee khalkhalka ayaa laga yaabaa inay sarreeyaan. Trisomy 18 wuxuu saameeyaa shakhsiyaadka dhammaan asalka jinsiyadeed.

Astaamaha

Trisomy 18 ayaa si ba'an u saameeya dhammaan hababka jirka ee jirka. Astaamaha waxaa ka mid noqon kara:

Ciladeynta

Hase-yeeshe, ilmaha badankood waxaa laga helaa dhalashada ka hor amniocentesis ( baaritaanka hidda-socodka dheecaanka amniotic).

Ultrasounds ee wadnaha iyo caloosha ayaa ogaan kara cillado aan caadi ahayn, sida x-ray-yaraha qalfoofka.

Daaweynta

Daryeel caafimaad oo loogu talagalay shakhsiyaadka leh Trisomy 18 waa taageero, oo diiradda saaraya bixinta nafaqada, daaweynta cudurrada, iyo maareynta dhibaatooyinka wadnaha.

Bilaha hore ee nolosha, dhallaanka qaba Trisomy 18 waxay u baahan yihiin daryeel caafimaad oo xirfad leh.

Sababtoo ah dhibaatooyinka caafimaad ee adag, oo ay ku jiraan cilladaha wadnaha iyo infakshanka ba'an, dhallaanka badankood waxay ku adagtahay sidii ay uga badbaadi lahaayeen da'da 1 sano. Horumarka daryeelka caafimaadka waqti ka dambeeya, mustaqbalka, waxay ka caawineysaa ilmaha badan ee leh Trisomy 18 inay ku noolaadaan carruurnimada iyo ka sii fog.

Xigasho:

"Waa maxay Trisom 18?" Hay'ada Trisomy 18 Foundation. 7 Apr 2009.

Waxaa soo diyaariyay Richard N. Fogoros, MD