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Article
Open AccessIdentification of novel KIF11 mutations in patients with familial exudative vitreoretinopathy and a phenotypic analysis
KIF11 gene mutations cause a rare autosomal dominant inheritable disease called microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR). Recently, such mutations were also found ...
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Article
Open AccessEarly onset coats’ disease initially treated as unilateral ROP at 39 weeks postmenstrual age: a case report
This is the youngest case of Coats’ disease, in terms of postmenstrual age (PMA), to be reported in the literature. This case highlights the remarkable variations in the clinical manifestations and the very ea...
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Article
The characteristics of digenic familial exudative vitreoretinopathy
To describe and analyse the clinical and genetic characteristics of digenic familial exudative vitreoretinopathy (FEVR).
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Article
Open AccessRetinal vein occlusion with cerebral infarction in a preterm neonate: a case report
Retinal vein occlusion (RVO) is a common disease that causes blindness in elderly patients, and cerebral infarction is also a severe disorder impairing the health of individuals. Both diseases are not common i...
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Article
Open AccessSerum levels of anti-Müllerian hormone influence pregnancy outcomes associated with gonadotropin-releasing hormone antagonist treatment: a retrospective cohort study
As a specific predictor of ovarian reserve, serum anti-Müllerian hormone (AMH) has become an area of intense research interest in the field of assisted reproductive technology. We assessed the relationship bet...
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Article
Research on ciphertext speech biohashing authentication based on chaotic system and improved public chain
Existing biohashing authentication schemes usually store bioinformation in the cloud, whose storage method can face the problems of bioinformation leakage and tampering, and single point of failure. To address...