6卷 第1期
1.Department of Ophthalmology & Otorhinolaryngology, Qilin District People's Hospital, Qujing, Yunnan, 655000, China
2.Department of Ophthalmology, Yunnan Provincial Maternal and Child Health Hospital, Kunming, Yunnan, 650051, China
纸质出版：2026-03-30
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Linhong Lei & Dan Tao. (2026). Research Advances in Genetic Diagnosis of Systemic Diseases Associated with Early-Onset High Myopia. 生物医学大数据, 6(1), 122-125.
Lei Linhong,Tao Dan.Research Advances in Genetic Diagnosis of Systemic Diseases Associated with Early-Onset High Myopia[J].Biomedical Data Science,2026,06(01):122-125.
Linhong Lei & Dan Tao. (2026). Research Advances in Genetic Diagnosis of Systemic Diseases Associated with Early-Onset High Myopia. 生物医学大数据, 6(1), 122-125. DOI： 10.47297/wspbdsWSP2752-630527.20260601.
Lei Linhong,Tao Dan.Research Advances in Genetic Diagnosis of Systemic Diseases Associated with Early-Onset High Myopia[J].Biomedical Data Science,2026,06(01):122-125. DOI： 10.47297/wspbdsWSP2752-630527.20260601.
In recent years
as myopia has shown a trend towards onset at younger ages
ophthalmologists have begun to pay high attention to early-onset high myopia (eoHM) in children. Childhood high myopia is a condition closely associated with ocular and systemic diseases. Studies have found that approximately 54% of children with high myopia have accompanying systemic diseases. eoHM is typically closely related to genetic factors and is often comorbid with syndromes. Often
before high myopia is diagnosed
the underlying systemic disease may remain undiagnosed. Therefore
eoHM also serves as an important clue for the early clinical identification of potential systemic diseases. With the rapid development of genetic testing technologies
ophthalmologists have gained a deeper understanding of genes related to systemic diseases associated with eoHM. Strengthening its genetic diagnosis and research is crucial for the early prevention
early diagnosis
timely treatment
and long-term management of both vision and systemic diseases in children with eoHM. Furthermore
for children with eoHM
the collaboration of multidisciplinary teams is necessary to ensure the timely detection and treatment of possible syndrome-associated disorders caused by genetic factors
jointly completing the diagnostic and therapeutic work
and improving the management system for blinding complications of eoHM. This will ultimately provide children with reasonable and precise treatment
enhancing their visual quality and quality of life.
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