Pehea e mālama ai i ka lipodystrophy congenital āpau

Anter

• Nā ʻōuli o lipodystrophy congenital āpau
• ʻIke o lipodystrophy kōmike nui

ʻO ka mālama ʻana no ka lipodystrophy congenital āpau, kahi maʻi genetical e ʻae ʻole i ka hōʻiliʻili o ka momona ma lalo o ka ʻili e alakaʻi ai i ka hōʻiliʻili ʻana o nā meaola a i ʻole nā ​​mākala, e manaʻo e hōʻemi i nā hōʻailona a, no laila, ʻokoʻa i kēlā me kēia hihia. Eia nō naʻe, hana ʻia ka hapa nui o ka manawa me:

• ʻAiʻai Carbohidate, e like me ka berena, laiki a i ʻole nā ​​uala: kōkua i ka mālama ʻana i nā pae ikehu i loko o ke kino i hoʻemi ʻia no ka nele o ka momona, e ʻae ana i ka ulu maʻamau a me ka ulu ʻana;
• Nā meaʻai momona momona: kōkua i ka pale ʻana i ka hōʻiliʻili ʻana o ka momona i nā mākala a me nā mea e like me ke ake a i ʻole pancreas. Eia ka mea e hōʻalo ai: Nā meaʻai kiʻekiʻe i ka momona.
• Leptin hope hoʻōla: nā lāʻau, e like me Myalept, hoʻohana ʻia e pani i ka hōmona i hana ʻia e nā momona momona, kōkua i ka pale ʻana i ka hoʻomaka ʻana o ka maʻi kō a i ʻole nā ​​pae kiʻekiʻe o nā triglycerides.

Hoʻohui ʻia, hoʻopili pū ʻia ka lapaʻau me ka hoʻohana ʻana i nā lāʻau no ka maʻi kō a me nā pilikia o ke ake, inā ua ulu mua kēia mau pilikia.

I nā hihia ʻoi loa, kahi lipodystrophy congenital laulā e hoʻopōʻino ai i ka ate a i ʻole nā ​​loli i ka maka, hiki ke hoʻohana ʻia ke ʻoki e hoʻoponopono i nā mea hoʻonaninani o ke alo, e hemo i nā liona ate a i ʻole nā ​​hihia ʻoi aku ka nui, e loaʻa kahi transplant. o ke akepaʻa.

Nā ʻōuli o lipodystrophy congenital āpau

ʻO nā ʻōuli o ka lipodystrophy congenital laulā, ʻike ʻia ʻo Berardinelli-seip Syndrome, ʻike pinepine ʻia i ka wā kamaliʻi a ʻike ʻia e ka nele o ka momona o ke kino e hāʻawi i kahi helehelena muscular me nā aʻa protruding. Hoʻohui, hōʻike paha ke keiki i ka ulu wikiwiki loa, e alakaʻi ana i ka ulu ʻana o nā lima, nā wāwae a i ʻole nā ​​iwi ā i nui loa no ko lākou mau makahiki.

I loko o nā makahiki, inā ʻaʻole mālama pono ʻia ka lipodystrophy congenital, hiki iā ia ke kumu i ka hōʻiliʻili o ka momona i nā mākala a i ʻole nā ​​kino, e alakaʻi ana i nā hopena e like me:

• Nui loa a hoʻomohala nā mākala;
• Poino nui ka ate;
• ʻAno 2 diabetes;
• Mānoanoa o ka puʻuwai puʻuwai;
• Nā pae kiʻekiʻe o nā triglycerides i ke koko;
• Hoʻonui i ka nui o ka spleen.

Ma waho aʻe o kēia mau pilikia, hiki i ka lipodystrophy congenital laulā ke hana i ka ulu ʻana o nā acigosis nigricans, kahi pilikia o ka ʻili e alakaʻi ai i ka hoʻomohala ʻana o nā pāʻeleʻele a mānoanoa ma ka ʻili, ʻo ia hoʻi ma ka ʻāʻī, ka ʻūlima a me ka ʻehaʻeha. E aʻo hou ma: Pehea e mālama ai i nā acigosis nigricans.

ʻIke o lipodystrophy kōmike nui

ʻO ka hōʻailona o ka lipodystrophy congenital laulā e hana ʻia e kahi mea hana maʻamau a endocrinologist paha, e ka nānā ʻana i nā ʻōuli a i ʻole ka loiloi ʻana i ka mōʻaukala o ka mea maʻi, ʻoiai inā lahilahi ka mea maʻi akā loaʻa nā pilikia e like me ka maʻi diabetes, nā triglycerides kiʻekiʻe, nā ʻino a me nā nigricans acanthosis. laʻana.

Hoʻohui ʻia, kauoha paha ke kauka i kekahi mau hōʻoia diagnostic e like me nā hoʻokolohua koko a i ʻole MRI, e nānā i nā pae lipid o ke koko a i ʻole ka luku ʻia o nā momona momona i loko o ke kino, no ka laʻana. I kekahi mau hanana kakaikahi loa, hiki ke hana ʻia kahi hoʻokolohua kūlohelohe e ʻike ai inā aia kahi hoʻololi i nā genes kikoʻī e kumu i ka lipodystrophy congenital ākea.

Inā hōʻoia ʻia ka hōʻailona o ka lipodystrophy congenital laulaha, pono e hāʻawi ʻia nā ʻōlelo aʻoaʻo kūʻē ma mua o ka hāpai ʻana, no ka laʻana, no ka mea aia ka pilikia o ka hoʻoili ʻana i ka maʻi i nā keiki.