I-Syndrome Apera - isifo esiyinkimbinkimbi yesifo

I-Syndrome Apera - isifo esingavamile, esibonakaliswe kwelinye lamasana angama-20,000. Le yintlupheko yesifo se-genetic esichazwe ngenguqu ekubunjeni kwekhayi, ngenxa ye-synostosis engaphambi kwexesha le-sutures ye-cranial, kunye neendlela ezingaphumeleli ekuphuhlisweni kweengalo, oko kukuthi i-symmetrical syndactyly yezandla kunye neenyawo (ukuphelelisa okupheleleyo okanye okuncinane kweminwe okanye inyawo).

Ngethuba lokuqala le ntlupheko yabonakaliswa ngugqirha waseFransi uApert ngowe-1906, ebukela abantwana abatsha abasenokusola kwesi sifo. U-Apert wafumanisa iimpawu zakhe kwaye wachaza le syndrome.

I-Syndrome ye-Aper: izizathu zophuhliso

I-Syndrome Apera, enezizathu ezingabonakaliyo, zingafumana ilifa. I-syndrome ye-Apera ngamanye amaxesha ngenxa yokokuba ngexesha lokukhulelwa, umama ozayo unokufumana isifo: i-rubella, umkhuhlane, i- meningitis, isifo sofuba okanye i-X-ray irradiation.

I-Syndrome ye-Apera: imiqondiso yekliniki

Kwizigulane ezine-syndrome ye-Aper, kukho ukungaqhelekanga kokuphuhliswa kwekhayi kunye nezinye iimpawu zempawu:

• "Inqaba" yokukhula kwentloko ngokukodwa ngokuphakama;
• Intloko ephakamileyo neyaziwayo, iindlebe ezinkulu;
• Umgca wephepheni;
• Ukusekwa ngokujulileyo kunye nohlobo olubanzi;
• Ngenxa yeziseko zamehlo ezisezantsi, uphuhliso lwe-puchoglazia;
• Ngokuqhelekileyo ukuhlukana kwezulu - "umlomo wempisi";
• Ukuhlanganiswa kweminwe ezandleni nasezinyaweni, kwindawo yesigxina, iinduli;
• Ukuphuhliswa kokuqina kumalungu amakhulu;
• Hlala ekuphuculweni ngokomzimba nangokwengqondo;
• Ngokuqhelekileyo kukho ukukhula kancinci, kukho ukulahlekelwa kwindlebe, ukusuleleka kwintsholongwane, i-anomalies kwisakhiwo se-pancreas kunye neentso;
• Utshintsho oluthile kwiimeko kunye nophuhliso lwe-cataracts, strabismus, nystagmus, ptosis.

Ukuxilongwa kwe-Aper's syndrome kuqala kwenzelwa ukubonakala kwesigulane. Isigulane sivavanywa kusetyenziswa ukuhlolwa kofuzo.

I-Syndrome ye-Apera: ifoto yesigulane

Iifoto ezinikezelwe kwinqaku yindlela efanelekileyo yokuthetha ngokubonakala kwesigulane.

I-Syndrome Apera: unyango

Unyango oluthile lwe-syndrome ye-Apera alukho, kodwa unonophelo lotyando luyimfuneko ekukhuseleni nasekulungiseni ukukhubazeka ngokomzimba kunye nokulinda kwengqondo. Ingundoqo yokusebenza ekuvaleni i-corutary sutures, ukuxinwa kwengcinezelo ye-intracranial, nayo iyadingeka kunye ne-orthodontic intervention intervention.

Imisebenzi yokuphanda kwixesha elizayo ijoliswe ekufomeni iminwe kwimigangatho ephezulu nangaphezulu. Ngokuqhelekileyo kukho ukuhlanganiswa kwesalathisi, phakathi kunye neminwe ngenxa yeethambo ezincinci kunye namathambo. Abagqirha benza imisebenzi yokuhlukanisa iminwe komnye kunye nokwandisa ukusebenza kwabo.

Unyango luyenziwa kuphela ngendlela edibeneyo. Iqela loogqirha lubandakanya oogqirha be-craniofacial, i-neurosurgeons, i-otolaryngologist, i-oculist, ugqirha wamazinyo, o-orthodontist, onika inkxaso ngoncedo.

Imisebenzi eyenza ubomi kube lula kwizigulane nge-Aper's syndrome zibavumela ukuba bafumene ubuchule bokwenyama nangokwengqondo, bafumane ukubonakala okuqhelekileyo, bathuthukise umgangatho wobomi kwaye baqaphele kuluntu.