Isifo seSchinzel-Giedion

Umxholo

• Iimpawu zeSchinzel-Giedion Syndrome
• Ungayinyanga njani iSchinzel-Giedion Syndrome

I-Schinzel-Giedion Syndrome sisifo esinqongopheleyo sokubeleka esizisa ukubonakala kokungalunganga kwamathambo, utshintsho ebusweni, ukuphazamiseka kwendlela yokuchama kunye nokulibaziseka okukhulayo kosana.

Ngokubanzi, iSchinzel-Giedion Syndrome ayisiyofuzo kwaye, ngenxa yoko, inokuvela kwiintsapho ezingenayo imbali yesi sifo.

THE Ischinzel-Giedion syndrome ayinyangi, kodwa utyando lunokwenziwa ukulungisa ukungalungi kunye nokuphucula umgangatho wobomi wosana, nangona kunjalo, ixesha lokuphila liphantsi.

Iimpawu zeSchinzel-Giedion Syndrome

Iimpawu zeSchinzel-Giedion Syndrome zibandakanya:

• Ubuso obumxinwa nebunzi elikhulu;
• Umlomo nolwimi olukhulu kunokuqhelekileyo;
• Uboya obuninzi bomzimba;
• Iingxaki ze-Neurological, ezinjengokungaboni kakuhle, ukuxhuzula okanye ukungeva;
• Utshintsho olukhulu entliziyweni, kwizintso okanye kwilungu lobufazi.

Ezi mpawu zihlala zichongwa kwakamsinya emva kokuzalwa kwaye, ke ngoko, umntwana kungafuneka alaliswe esibhedlele ukuze anyange ezo mpawu ngaphambi kokuba aphume kwisibhedlele sokubeleka.

Ukongeza kwiimpawu zesi sifo, iintsana ezineSchinzel-Giedion syndrome nazo ziba nenkinga yokuwohloka kwemithambo-luvo, umngcipheko okhulayo wamathumba kunye nosulelo oluphindaphindeneyo lokuphefumla, njenge-pneumonia.

Ungayinyanga njani iSchinzel-Giedion Syndrome

Akukho lunyango lunyangayo lokunyanga iSchinzel-Giedion Syndrome, nangona kunjalo, ezinye iindlela zonyango, ngakumbi utyando, zinokusetyenziselwa ukulungisa ukungalunganga okubangelwe sesi sifo, ukuphucula umgangatho wobomi bosana.