The case of a 35-year-old man who presented with sudden-onset generalized tonic-clonic seizures highlights that FLAMES may be complicated by postictal purpura and rhabdomyolysis, underscoring the potential for diagnostic confusion with systemic inflammatory disease.
Shang Xiang, Dai-Ping Hua, Shih-Hung Yang et al.· Frontiers in Immunology· 0 citations
Pseudohypoparathyroidism (PHP) type 1A is a rare inherited disorder characterized by resistance to parathyroid hormone and, typically, features of Albright hereditary osteodystrophy. We report a late-onset case in a 59-year-old woman who presented with cognitive decline, behavioral and psychiatric symptoms, gait instab...
Dai-Ping Hua, Shang Xiang, Xian-Feng Yu et al.· Frontiers in Endocrinology· 0 citations
Wilson disease (WD) is a hereditary disorder of copper metabolism caused by mutations in the ATP7B gene; the Chinese population exhibits a unique, high-frequency mutation profile centered on the R778L and P992L mutations. This article provides a narrative review of the genetic evolution, molecular pathogenic mechanisms...
Qiaoyu Xuan, Daiping Hua, Lanting Sun et al.· Frontiers in Molecular Biosc...· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.