ISSN 3060-4745 Open Access · Peer Reviewed
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Keywords

Albinizm, melanin, irsiy kasallik, OCA, OA, genetik mutatsiya, pigmentatsiya, ko‘z kasalliklari, dermatologiya, tashxis.

How to Cite

“ALBINIZM KASALLIGI: GENETIK MEXANIZMLARI, TURLARI VA IJTIMOIY TA’SIRLARI”. (2025). ACUMEN: INTERNATIONAL JOURNAL OF MULTIDISCIPLINARY RESEARCH, 2(7), 68-70. https://www.universalpublishings.com/index.php/aijmr/article/view/13288

Abstract

Ushbu maqolada albinizm kasalligining genetik sabablari, klinik turlari, tashxislash usullari va ijtimoiy-psixologik oqibatlari ko‘rib chiqiladi. Albinizm — bu irsiy kasallik bo‘lib, unda organizmda pigment (melanin) sintezining buzilishi natijasida teri, soch va ko‘zlarda oqish rang paydo bo‘ladi. Maqolada OCA va OA shakllari, ularning farqlari, tashxis va davolash usullari ilmiy manbalar asosida tahlil qilinadi. Albinizmi bo‘lgan shaxslarning jamiyatdagi diskriminatsiyasi, ko‘rish muammolari va iqlim ta’siriga sezuvchanligi ham yoritiladi.

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References

1. Grønskov, K., Ek, J., & Brondum-Nielsen, K. (2007). Oculocutaneous albinism. Orphanet Journal of Rare Diseases, 2(1), 43.

2. Montoliu, L., & Kelsh, R. N. (2014). Albinism in humans and other animals:

3. recent advances in understanding their development, genetics, and evolution. Pigment Cell & Melanoma Research, 27(1), 54-61.

4. Summers, C. G. (2009). Vision in albinism. Transactions of the American Ophthalmological Society, 107, 282

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