Discover Breviturma securis, a newly identified brittle star species along Taiwan’s coast, featuring spiny arms and unique axe-shaped patterns.

Researchers from University College London (UCL) are aiming to develop potential treatments for congenital muscular dystrophy (CMD) after being awarded a £1m grant from LifeArc and Muscular Dystrophy ...

Myotonic dystrophy type 1 (DM1) is a form of muscular dystrophy caused by DMPK mutations on chromosome 19. It affects muscles and many organs across multiple systems that depend on muscular activity.

PD is usually associated with a good prognosis, unless rarely complicated by CNV (highly responsive to anti-VEGF agents). Several different fundus appearances have been described based on the variable ...

Characteristic features included pattern dystrophy-like changes (P14, P5), peripapillary atrophy (P14, P5, P18), reticular pseudodrusen (P5), angioid streaks and atrophy (P18). These features could ...

Givinostat Receives Full FDA Approval for Duchenne Muscular Dystrophy In March, the FDA approved givinostat (Duvyzat) for boys aged 6 years and older with DMD, marking it as the first nonsteroidal ...

Fuchs’ dystrophy tends to affect older people who may also have cataracts. When a cataract is the primary reason for decreased vision, cataract surgery may be performed alone.

Facioscapulohumeral muscular dystrophy (FSHD) is a genetic condition that can lead to the slow deterioration of muscles, predominantly in the face, shoulder blades, and upper arms.

Hodgkin’s lymphoma, lymphocyte-depleted, reticular: An NCDB analysis of demographic and socioeconomic factors of diagnosed patients.. JCO 42 , e19033-e19033 (2024). DOI: ...