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8 Mins
14 Dec 2023

Spasticity Following Acute Stroke

Many patients experience impairment following a stroke, including motor or cognitive impairment, urinary incontinence, dysphagia…
8 Mins
14 Dec 2023

Tackling Becker Muscular Dystrophy

First described by German physician Peter Emil Becker in the 1950s, Becker is an X-linked genetic recessive disorder. Like Duchenne…
7 Mins
20 Nov 2023

A Review of Oral Fixed-Dose Sodium Phenylbutyrate and Ursodoxicoltaurine in People with Amyotrophic Lateral Sclerosis

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that is estimated to affect approximately 300,000 individuals worldwide…
11 Mins
4 Oct 2023

Lennox–Gastaut Syndrome: Challenges in Diagnosis – Interviews with Two Key Opinion Leaders

Lennox–Gastaut syndrome (LGS) is a severe childhood-onset epilepsy syndrome that can be challenging to identify due to its heterogeneous and..
13 Mins
14 Sep 2023

The Unspeakable Disease: A Tale of Two Siblings

The deficiency of arylsulfatase A due to the mutations in the ARSA gene is the cause of a rare inherited lysosomal storage disease…
6 Mins
14 Sep 2023

Assessment of Post-Traumatic Stress Disorder in Patients Who Recovered from COVID-19

It is essential to address psychological health, particularly post-traumatic stress disorder (PTSD), among patients who have recovered from…
11 Mins
15 Aug 2023

Focal Onset Seizures: New Treatment Options in The Clinical Practice

Carreño began by discussing the spectrum of uncontrolled epilepsies. They stressed that uncontrolled epilepsy does not necessarily…
9 Mins
15 Aug 2023

A Spotlight on Friedreich Ataxia: Optimising the Patient Journey from Diagnosis to Disease Management

Boesch explained that in the European Union (EU), a rare disease is defined as a disease that affects less than one person in 2,000…