Human genetic diagnostics in hereditary eye diseases What does the ophthalmologist need to know

被引:1
|
作者
Neuhann, Teresa M. [1 ,3 ]
Neuhann, Lukas [2 ]
机构
[1] MGZ Med Genet Zent, Munich, Germany
[2] MVZ Prof Neuhann, Munich, Germany
[3] MGZ Med Genet Zent, Bayerstr 3-5, D-80335 Munich, Germany
来源
OPHTHALMOLOGIE | 2023年 / 120卷 / 06期
关键词
Ophthalmic genetics; Panel testing; Gene therapy; Exome; Genome; HIGH MYOPIA; MUTATIONS; PROBANDS;
D O I
10.1007/s00347-023-01878-6
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Hereditary eye disorders can affect all ocular structures and can be accompanied by structural malformations (e.g. coloboma) or functional disorders (e.g. retinal dystrophy). Ocular phenotypes can also be the presenting symptom of many complex syndromic disorders. The majority of hereditary eye disorders are extremely heterogeneous but can be routinely diagnosed by modern high-throughput sequencing technologies. Molecular testing is highly important not only in in the evaluation of differential diagnoses but is also of increasing relevance due to individual treatment options.
引用
收藏
页码:679 / 688
页数:10
相关论文
共 50 条