A clinical case of albinism in a 12 year old child
https://doi.org/10.25789/YMJ.2024.88.30
Abstract
The article presents a clinical follow-up of a child with oculocutaneous albinism type 1A. For the first time, the type of albinism was established and concomitant diseases were identified. Oculocutaneous albinism is a disease with an autosomal recessive type of inheritance, in which, in addition to ocular albinism, there is hypopigmentation of the skin and hair.
About the Authors
M. S. Savvina
ЯНЦ КМП
Russian Federation
Russian Federation
O. N. Ivanova
МИ СВФУ им. М.К. Аммосова
Russian Federation
Russian Federation
G. M. Melchanova
ПЦ РБ№1 – НЦМ
Russian Federation
Russian Federation
T. E. Burtseva
МИ СВФУ; ЯНЦ КМП
Russian Federation
Russian Federation
I. S. Ivanova
МИ СВФУ
Russian Federation
Russian Federation
M. P. Slobodchikova
СПб ГПМУ
Russian Federation
Russian Federation
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Review
For citations:
Savvina M.S., Ivanova O.N., Melchanova G.M., Burtseva T.E., Ivanova I.S., Slobodchikova M.P. A clinical case of albinism in a 12 year old child. Yakut Medical Journal. 2024;(4):124-126. (In Russ.) https://doi.org/10.25789/YMJ.2024.88.30
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