Umbhali: Roger Morrison
Umhla Wokudalwa: 2 Eyomsintsi 2021
Hlaziya Umhla: 12 Eyenkanga 2024
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Umxholo

Ukutya kwe-phenylketonurics ngakumbi ezo zinamaxabiso asezantsi e-amino acid phenylalanine, ezinje ngeziqhamo kunye nemifuno kuba abaguli abanesi sifo abanako ukuhambisa iamino acid.

Ezinye iimveliso ezinamashishini zinolwazi lweelebhile malunga nobukho be-phenylalanine kwimveliso kwaye yintoni ubungakanani bayo, njenge-agar gelatin, isiselo esingenakutya, isiselo se popsicle, iswekile okanye isitashi, umzekelo, kubalulekile ukuba isigulana okanye abazali besigulana bajonga iilebheli zokutya nokuba ukutya akunayo i-phenylalanine okanye kangakanani.

Itafile yokutya ye-phenylketonurics

Itshathi yokutya ye-phenylketonurics inexabiso le-phenylalanine kukunye ukutya.

UkutyaLinganisaInani le phenylalanine
Irayisi ephekiweyo1 icephe28 mg
Iifatata ezimnandi zamazambane1 icephe35 mg
Icassava ephekiweyo1 icephe9 mg
Ilethasi1 icephe5 mg
Itumato1 icephe13 mg
I-broccoli ephekiweyo1 icephe9 mg
Iminqathe eluhlaza1 icephe9 mg
IponyoponyoIyunithi e-1206 mg
ikiwiIyunithi e-138 mg
apileIyunithi e-115 mg
Ibhasikithi uMaria / MaisenaIyunithi e-123 mg
Ukhilimu wobisi1 icephe44 mg
Ibhotolo1 icephe11 mg
Imajarini1 icephe5 mg

Inani le phenylalanine elivunyelweyo ngosuku liyahluka ngokobudala besigulana kunye nobunzima. Isondlo sokutya senza imenyu ngokwenani elivunyelweyo le-phenylalanine elibandakanya konke ukutya kunye nendlela yokulungiselela ukuququzelela ukuqonda kunye nokubambelela kunyango lwezigulana kunye nabazali kwimeko yabantwana.


Ukutya okuThintelweyo ePhenylketonuria

Ukutya okune-phenylalanine engaphezulu akususwanga ekutyeni, kodwa kudliwe ngexabiso elincinci kakhulu elimiselwe ngumondli ohamba nesigulana kwaye:

  • Inyama, intlanzi kunye neqanda;
  • Iimbotyi, umbona, iilentile, iichickpeas;
  • Amandongomane;
  • Ingqolowa kunye ne-oat flour;
  • Imveliso yokutya esekwe kwi-aspartame.

Kuyimfuneko ukunqanda ukutya okulungiselelwe ngezi zinto, ezinje ngeekeyiki, iicookies kunye nezinye.

Amakhonkco aluncedo:

  • Phenylketonuria
  • Ukutya kwe-phenylketonuria

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