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1.
Clin Genet ; 97(5): 747-757, 2020 05.
Artículo en Inglés | MEDLINE | ID: mdl-32022900

RESUMEN

FLNC-related myofibrillar myopathy could manifest as autosomal dominant late-onset slowly progressive proximal muscle weakness; involvements of cardiac and/or respiratory functions are common. We describe 34 patients in nine families of FLNC-related myofibrillar myopathy in Hong Kong ethnic Chinese diagnosed over the last 12 years, in whom the same pathogenic variant c.8129G>A (p.Trp2710*) was detected. Twenty-six patients were symptomatic when diagnosed; four patients died of pneumonia and/or respiratory failure. Abnormal amorphous material or granulofilamentous masses were detected in half of the cases, with mitochondrial abnormalities noted in two-thirds. We also show by haplotype analysis the founder effect associated with this Hong Kong variant, which might have occurred 42 to 71 generations ago or around Tang and Song dynasties, and underlain a higher incidence of myofibrillar myopathy among Hong Kong Chinese. The late-onset nature and slowly progressive course of the highly penetrant condition could have significant impact on the family members, and an early diagnosis could benefit the whole family. Considering another neighboring founder variant in FLNC in German patients, we advocate development of specific therapies such as chaperone-based or antisense oligonucleotide strategies for this particular type of myopathy.


Asunto(s)
Filaminas/genética , Músculo Esquelético/patología , Miopatías Estructurales Congénitas/genética , Adulto , Anciano , Pueblo Asiatico , Electromiografía , Femenino , Efecto Fundador , Hong Kong/epidemiología , Humanos , Masculino , Persona de Mediana Edad , Debilidad Muscular/diagnóstico por imagen , Debilidad Muscular/genética , Debilidad Muscular/patología , Músculo Esquelético/diagnóstico por imagen , Mutación/genética , Miopatías Estructurales Congénitas/epidemiología , Miopatías Estructurales Congénitas/patología , Linaje , Fenotipo
2.
Opt Lett ; 45(4): 791-794, 2020 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-32058471

RESUMEN

Microdisks are excellent whispering-gallery mode (WGM) optical resonators, but their emissions are invariably in-plane isotropic due to their circularities and thus difficult to be extracted efficiently. In this work, a waveguide with a width of 0.16 µm directly coupled to a microdisk with a diameter of 10 µm is fabricated on a 0.77 µm thick GaN thin film containing InGaN/GaN multi-quantum wells. This eliminates the need for precision patterning required by evanescent coupling schemes in which coupling gaps of the order of tens of nanometers must be maintained. The fabrication was carried out using nanosphere and nanowire lithography. Non-evanescent coupling of WGMs to the waveguide from the microdisk is successfully demonstrated.

3.
Emerg Infect Dis ; 23(4): 665-668, 2017 04.
Artículo en Inglés | MEDLINE | ID: mdl-28322697

RESUMEN

Human sparganosis is a foodborne zoonosis endemic in Asia. We report a series of 9 histologically confirmed human sparganosis cases in Hong Kong, China. All parasites were retrospectively identified as Spirometra erinaceieuropaei. Skin and soft tissue swelling was the most common symptom, followed by central nervous system lesions.


Asunto(s)
Esparganosis/epidemiología , Esparganosis/parasitología , Spirometra/aislamiento & purificación , Adulto , Anciano , Animales , Femenino , Parasitología de Alimentos , Hong Kong/epidemiología , Humanos , Masculino , Persona de Mediana Edad , Spirometra/clasificación , Spirometra/genética , Zoonosis
4.
Opt Lett ; 39(19): 5614-7, 2014 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-25360941

RESUMEN

Optically pumped multi-mode whispering-gallery mode (WGM) lasing has been observed in optically free-standing InGaN/GaN quantum well microdisks at room temperature. The ∼6.6 µm optically isolated microdisks are patterned by microsphere lithography on GaN thin-films prepared by laser lift-off of the sapphire substrate, enabling superior optical confinement. The modes are determined to be of second order according to simulations. The lasing threshold is found to be ∼9.06 mJ/cm2, with a quality factor Q of ∼770 evaluated from the dominant mode at λ=430.2 nm, and a free space range (FSR) of 3.17 to 2.16 nm, which is mode-dependent.

5.
Orphanet J Rare Dis ; 18(1): 43, 2023 03 02.
Artículo en Inglés | MEDLINE | ID: mdl-36859275

RESUMEN

OBJECTIVE: To determine the prevalence of mitochondrial diseases (MD) in Hong Kong (HK) and to evaluate the clinical characteristics and genetic landscape of MD patients in the region. METHODS: This study retrospectively reviewed the phenotypic and molecular characteristics of MD patients from participating public hospitals in HK between January 1985 to October 2020. Molecularly and/or enzymatically confirmed MD cases of any age were recruited via the Clinical Analysis and Reporting System (CDARS) using relevant keywords and/or International Classification of Disease (ICD) codes under the HK Hospital Authority or through the personal recollection of treating clinicians among the investigators. RESULTS: A total of 119 MD patients were recruited and analyzed in the study. The point prevalence of MD in HK was 1.02 in 100,000 people (95% confidence interval 0.81-1.28 in 100,000). 110 patients had molecularly proven MD and the other nine were diagnosed by OXPHOS enzymology analysis or mitochondrial DNA depletion analysis with unknown molecular basis. Pathogenic variants in the mitochondrial genome (72 patients) were more prevalent than those in the nuclear genome (38 patients) in our cohort. The most commonly involved organ system at disease onset was the neurological system, in which developmental delay, seizures or epilepsy, and stroke-like episodes were the most frequently reported presentations. The mortality rate in our cohort was 37%. CONCLUSION: This study is a territory-wide overview of the clinical and genetic characteristics of MD patients in a Chinese population, providing the first available prevalence rate of MD in Hong Kong. The findings of this study aim to facilitate future in-depth evaluation of MD and lay the foundation to establish a local MD registry.


Asunto(s)
Pueblo Asiatico , Enfermedades Mitocondriales , Humanos , Hong Kong , Prevalencia , Estudios Retrospectivos
6.
Mov Disord ; 22(7): 1038-43, 2007 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-17357133

RESUMEN

We describe an 84-year-old man with an unusual clinical presentation of palatal tremor in association with ciprofloxacin treatment. The patient had rhythmical movements not only of the soft palate but also of the face and trunk. Complete resolution of the symptoms occurred 2 days after discontinuation of ciprofloxacin and administration of sodium valproate. This is the first reported case of palatal tremor secondary to the use of ciprofloxacin.


Asunto(s)
Antiinfecciosos/efectos adversos , Ciprofloxacina/efectos adversos , Paladar Blando/efectos de los fármacos , Temblor/inducido químicamente , Anciano de 80 o más Años , Humanos , Imagen por Resonancia Magnética , Masculino , Literatura de Revisión como Asunto , Temblor/patología
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