Kallmann syndrome (KS) is a disorder characterized by hypogonadotropic hypogonadism and anosmia. Although KS is genetically heterogeneous, only two causal genes have been identified to date. These ...

For those of you that don't know what SMA 1 is, it is the most severe muscular disease that a baby can get," Jesy Nelson said ...

As of Wednesday, January 07, Design Therapeutics, Inc.’s DSGN share price has surged by 8.50%, which has investors questioning if this is right time to sell.

In an emotional Instagram video posted on Sunday, Ms Nelson revealed the girls had been diagnosed with spinal muscular ...

MUSCAT: The decision to mandate premarital medical examinations for all Omanis wishing to get married, as per Royal Decree No 111/2025, represents ...

Jesy Nelson has shared a new video of her twin daughters' early symptoms of with Spinal Muscular Atrophy (SMA1) as she ...

LYNX-3, the second pivotal Phase 3 trial in keratorefractive participants with visual disturbances under mesopic, low-contrast conditions, is ongoing with topline results expected in the first half of ...

AB Science receives US patent for masitinib to treat sickle cell disease: Paris Friday, December 26, 2025, 14:00 Hrs [IST] AB Science SA, a pharmaceutical company specializing in ...

Spinal muscular atrophy is a rare genetic disorder causing progressive muscle weakness, now in focus after Jesy Nelson shared her twins' diagnosis.

Cat Deeley has branded Jesy Nelson the 'strongest and bravest women she's met' after the singer opened up about her twins' ...

Ekaya Duncan, 24, CEO of Mainplug TV and a sickle cell warrior, explains that his journey with the condition began in infancy ...

Hereditary non-syndromic deafness has been associated with a point mutation in the mitochondrial 12S rRNA gene. We present data from deaf individuals in 12 nuclear families originating from a small ...