I-Parsley Syndrome - yintoni esi sifo kunye nendlela i-Angelmann syndrome ephathwa ngayo?

Ngokokuqala ngqa imbono yePetrushka syndrome yaqaliswa ngo-1965 nguHarry Angelmann, emva koko esi sigulo sagqithwa ngokubizwa ngegama. Ubunzima besi sifo unabantwana abayi-1 ukuya kuma-20 000 kwaye isasazwa ngokwezityalo. Esi sifo sifumaneka kwi minyaka engama-3-7 kwaye ngokuphindaphindiweyo kubafana.

I-Petrushka syndrome - yintoni na?

Esi sifo sabizwa ngokuthi "unonophelo lwe-doll syndrome", "udoli ohlekayo" okanye "i-puppet syndrome". Isifo sePetrushka sisifo esingaqhelekanga se-genetic geneticism, esichazwe ngokulibaziseka ekuphuhlisweni kwamakhono kunye nemvelo. Ukuseka ukukhubazeka nge-Angelman syndrome kunokwenzeka ukuba uyaphonononga uphando kwaye ufundise ukupheliswa kwezityalo. Isizathu sokungabikho kweendiza ze-chromosome ye-15, njengomthetho, kufuneka zifunwe kwi-genotype yomama. Kula mabhinqa, ithuba lokunyamezela umntwana ophilileyo luncinci kakhulu, ukuba ibhinqa lihlupheke kwesi sifo - kwi-98% yamatyala umntwana omnye uvela.

Ukuxilongwa kwe-angelman syndrome kwenziwa xa umntwana osandul 'ukuzalwa eswelekile kwimisebenzi ye-muscle kunye nokukhubazeka kwemoto. Ngelishwa, abantu abaneengxaki ezinjalo abanalo ithuba lokulungisa ngokupheleleyo, i-chromosome ye-15 ichaphazelekayo-ithuba elingaphantsi lokunyanga. Kuyaziwa ukuba eso sifo asizukufa nje kuphela, kodwa sibonakaliswe ngakumbi kunamandla ngakumbi ngakumbi kunomama.

Parsley Syndrome - Iimpawu

Esi sifo sibonakaliswe ngu:

Iimpawu kwizigulane zabantu abadala ziyancitshiswa ngaphezu kweminyaka. Xa bekhulile, bafumana iimpawu ezithile, ezifana nokuxhatshazwa nokuphazamiseka kokulala , kwaye ezinye ziba zibi nakakhulu, umzekelo, i-scoliosis. Xa uneminyaka yobudala, iingxaki zesisindo ziyaqala. Kwimantombazana eneli syndrome, ngexesha lokutshatyalaliswa kwexesha, eqhubeka ngexesha eliqhelekileyo, kunokubakho ukwanda kwintlungu.

Angelman Syndrome kubantwana - iimpawu

Impawu zokuqala ze-parsley syndrome zivele zivele kwiinyanga zokuqala zophuhliso.

  1. Kwiingxaki zokutya, ukulala, ukunciphisa ukufumana ubunzima. Isidingo sokulala singancipha, kwaye ulawulo oluqhelekileyo alukwazi ukusekwa ixesha elide.
  2. Esikolweni esikolweni kuya kuba neengxaki zokufunda nokuqonda, ubunzima bokugxininiswa kwengqalelo.
  3. Ukungahambelani nokufunda kunokuquka ukungahambi kakuhle, iingxaki zokuthetha kunye neengxaki zokusebenzisana.
  4. Ngenxa yokufumana imilenze elukhuni, izigulane zibizwa ngokuthi "iipiliti", zikwahlukana nokunyuka kwesifo, kunye nokugqithisileyo, ukugaya i-80% yezigulane.

Izifo "Parsley Syndrome" - bangaphi abahlala kuyo?

Ubomi bokulinda kwezigulane ezinokuxilongwa "kwePetrushka syndrome" buphakathi kweminyaka engama-35-40. Abantu abafumene ukukhubazeka, kodwa ngubani osebenzise isilungiso esifanelekileyo ixesha lonke, angaphila ixesha elide. Okwangoku, akukho zindlela zokuphilisa ngokupheleleyo, kodwa kukho iinkqubo ezizodwa ezingaphucula umgangatho wobomi bezigulane.

Angelman syndrome - unyango

Kubalulekile ukukhumbula ukuba into ebaluleke kakhulu kubantwana abanesifo esinjalo ngumoya wothando nothando ekhaya, musa ukulibala malunga neemviwo eziqhelekileyo kunye nokugcinwa kwazo zonke iimeko zonyango lokwelapha. Ngokuhamba kwexesha, iindlela ezintsha zokuphatha i-Anghelman's syndrome ziphuhliswa. Ezi nkqubo ezizodwa zenziwe ngabanye kwisigulane ngasinye ngesimpawu ezahlukeneyo, kodwa kukho iindlela ezine eziphambili:

  1. Anticonvulsants for therapy of stempile, eyokunciphisa umngcipheko wokubanjwa kwexesha eliqhelekileyo kunye nokunciphisa iziphumo.
  2. Imizimba ye-Physiotherapy yokuphuhlisa izakhono ezincinci zezithuthi kunye nezinye iintlobo zomsebenzi wemoto.
  3. Ulwimi lwezandla lungcono ukuqala ukufunda ukususela kwiminyaka yobudala, ukufunda indlela enxibelelwano kukuncedisa ukuba ulungelelanise uphinde unxibelelane ngokukhawuleza, ngokubanzi kunokwenzeka kule meko.
  4. Ulwaphulo lokuziphatha luyimfuneko ukunqoba ukunyanzelisa nokunyusa uxinzelelo.