Huijun Zhao, Yichao Shi, Xi Luo, Yurong Tan, Yunsheng Yang, Li‐Ping Zou
Tourette syndrome is a neuropsychiatric disorder with onset in childhood. New
therapies are needed to effectively manage and treat this condition. Gut
microbiota can affect central physiology and function via the
microbiota-gut-brain axis. Here, we report a case in which fecal microbiota
transplantation (FMT) is used to treat a child with Tourette syndrome, whose
symptoms ameliorated dramatically ... hiện toàn bộ
Alexander A. C. Leung, Alicia K.J. Chan, Justin A. Ezekowitz, Alexander K. C. Leung
3-hydroxy-3-methylglutaryl-coenzyme A (HMG CoA) lyase deficiency is an inborn
error of metabolism characterized by impairment of ketogenesis and leucine
catabolism resulting in an organic acidopathy. In 1994, a case of dilated
cardiomyopathy and fatal arrhythmia was reported in a 7-month-old infant. We
report a case of dilated cardiomyopathy in association with HMG CoA lyase
deficiency in a 23-yea... hiện toàn bộ
A case of xanthogranulomatous salpingitis (XGS) associated with a large uterine
leiomyoma in a 50-year-old woman is presented. Xanthogranulomatous inflammation
is an uncommon form of chronic inflammation that is destructive to affected
organs. It is characterized by the presence of lipid-filled macrophages with
admixed lymphocytes, plasma cells, and neutrophils. A review of the literature
revealed... hiện toàn bộ
Mast cell disorders are defined by an abnormal accumulation of tissue mast cells
in one or more organ systems. In systemic mastocytosis, at least one
extracutaneous organ is involved by definition. Although, systemic mastocytosis
usually represents with skin lesion called urticaria pigmentosa, in a small
proportion, there is extracutaneous involvement without skin infiltration. Other
manifestation... hiện toàn bộ
Neluwa-Liyanage R. Indika, Dinesha Maduri Vidanapathirana, Eresha Jasinge, Roshitha Waduge, N. L. A. Shyamali, Rasika Perera
Phosphatidate phosphatase-1 (lipin-1) is encoded by LPIN1 gene. Lipin-1
deficiency has been reported as the second most common cause of early-onset
rhabdomyolysis after primary fatty acid oxidation disorders. We report a case of
a 32-year-old Sri Lankan female with a history of more than 10 episodes of
rhabdomyolysis and exercise intolerance since childhood. These episodes were
triggered by infect... hiện toàn bộ
Ahmet Hakan Ateş, Uğur Arslan, Aytekin Aksakal, Huriye Yücel, İlksen Atasoy Günaydın, Adem Ekbul, Mehmet Yaman
Mitral balloon valvuloplasty which has been used for the treatment of rheumatic
mitral stenosis (MS) for several decades can cause serious complications.
Herein, we presented right atrial clot formation early after percutaneous mitral
balloon valvuloplasty which was treated successfully with unfractioned heparin
infusion.