The exact etiology of AD is unknown; however, it has beensuggested tha translation - The exact etiology of AD is unknown; however, it has beensuggested tha Indonesian how to say

The exact etiology of AD is unknown

The exact etiology of AD is unknown; however, it has been
suggested that genetic factors may contribute to errors in protein
synthesis resulting in formation of abnormal proteins
involved in the pathogenesis of AD.9 Early onset, which is
defined as AD prior to age 60, accounts for approximately 1%
of all AD. This type is usually familial and follows an autosomal
dominant pattern in approximately 50% of cases of early-onset
AD.Mutations in three genes, presenilin 1 on chromosome 21,
amyloid precursor protein (APP) on chromosome 21, and presenilin
2 on chromosome 1, lead to an increase in β-A4 peptide
fragments of APP which forms neuritic plaques that are
the pathologic hallmark of AD.
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Results (Indonesian) 1: [Copy]
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Etiologi tepat iklan tidak diketahui; Namun, itu telahmenyarankan bahwa faktor genetik mungkin berkontribusi terhadap kesalahan proteinsintesis mengakibatkan pembentukan protein abnormalterlibat dalam patogenesis onset awal AD.9, yang merupakandidefinisikan sebagai iklan sebelum usia 60, account untuk sekitar 1%Semua iklan. Jenis ini biasanya kekeluargaan dan mengikuti autosomalpola dominan di sekitar 50% dari kasus awal-awalIKLAN. Mutasi pada tiga gen, presenilin 1 pada kromosom 21,pendahulu amiloid protein (APP) pada kromosom 21, dan presenilin2 pada kromosom 1, mengakibatkan peningkatan peptida β-A4fragmen App yang membentuk plak neuritic yangciri patologis dari iklan.
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Results (Indonesian) 2:[Copy]
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Etiologi pasti dari AD tidak diketahui; Namun, telah
menyarankan bahwa faktor genetik dapat menyebabkan kesalahan dalam protein
sintesis menghasilkan pembentukan protein abnormal
yang terlibat dalam patogenesis AD.9 onset dini, yang
didefinisikan sebagai AD sebelum usia 60, menyumbang sekitar 1%
dari semua IKLAN. Jenis ini biasanya familial dan mengikuti autosomal
pola dominan pada sekitar 50% kasus awal-awal
AD.Mutations dalam tiga gen, Presenilin 1 pada kromosom 21,
prekursor amiloid protein (APP) pada kromosom 21, dan Presenilin
2 pada kromosom 1 , menyebabkan peningkatan β-A4 peptida
fragmen dari APP yang membentuk plak neuritik yang
ciri patologis dari AD.
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