Sungyeon Park
Biographic Data
| ID | 8263585 |
|---|---|
| NAME | Sungyeon Park |
| GIVEN NAMES | Sungyeon |
| FAMILY NAME | Park |
| SIGNATURE | PARK S |
| AFFILIATIONS | Kyungpook National University |
| VERIFIED | No |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 1 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2026 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
Episodic Ataxia Type 2 Presenting with Fluctuating Weakness in a Child with a De Novo Cacna1A Variant
Background: Episodic ataxia type 2 (EA2) is the most common subtype of episodic ataxia and is primarily caused by pathogenic variants in the CACNA1A gene. Although classically characterized by paroxysmal ataxia, CACNA1A-related disorders are increasingly recognized as an age-dependent phenotypic continuum that extends beyond episodic cerebellar dysfunction to include fluctuating weakness, persistent neurological signs, and neurodevelopmental impa…
No prominent works on this page.
Episodic Ataxia Type 2 Presenting with Fluctuating Weakness in a Child with a De Novo Cacna1A Variant
Background: Episodic ataxia type 2 (EA2) is the most common subtype of episodic ataxia and is primarily caused by pathogenic variants in the CACNA1A gene. Although classically characterized by paroxysmal ataxia, CACNA1A-related disorders are increasingly recognized as an age-dependent phenotypic continuum that extends beyond episodic cerebellar dysfunction to include fluctuating weakness, persistent neurological signs, and neurodevelopmental impa…
Ataxia (1 work) · Cerebellar ataxia (1 work) · Channelopathy (1 work) · Genetic Neurodegenerative Diseases (1 work) · Genomics and Rare Diseases (1 work) · Global developmental delay (1 work) · Glycogen Storage Diseases and Myoclonus (1 work) · Hypotonia (1 work) · Movement Disorders (1 work) · Paroxysmal dyskinesia (1 work)