Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Joanna Yuet-ling Tung"'
Autor:
Geoffrey Chek Fei Yu, Ming-kut Tay, Sammy Pak-lam Chen, Mei Tik Stella Leung, Joanna Yuet-ling Tung
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-6 (2023)
17α-hydroxylase deficiency (17α-OHD) is a rare form of congenital adrenal hyperplasia. We report the case of a teenage girl with 17α-OHD who presented with delayed puberty, hypergonadotropic hypogonadism and hypertension. We illustrate the clinica
Externí odkaz:
https://doaj.org/article/688785128ade49528d3b810904e9e1d9
Publikováno v:
Journal of Obesity & Metabolic Syndrome, Vol 31, Iss 3, Pp 272-276 (2022)
Background : With the growing obesity epidemic, subjecting every child with obesity to a 2-hour oral glucose tolerance test (OGTT) is impractical. Instead, 30-minute plasma glucose (PG), which reflects the acute phase of insulin secretion, might be a
Externí odkaz:
https://doaj.org/article/daf3a706ea7d4a90beb0b0cc86cd8f04
Autor:
Joshua Chun Ki Chan, Evelyn Eugenie Kuong, Joyce Pui Kwan Chan, Ho Ming Luk, Jasmine Lee Fong Fung, Joanna Yuet-ling Tung, Brian Hon Yin Chung
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare condition. The diagnosis could be challenging due to its rarity and non-specific presenting symptoms. However, early diagnosis and appropriate management help in preserving patients' functi
Externí odkaz:
https://doaj.org/article/0b16706a00c94464bd574f859eb4fbe5
Autor:
Joanna Yuet-ling Tung, Frederick Ka-wing Ho, Keith Tsz-suen Tung, Rosa Sze-man Wong, Wilfred Hing-sang Wong, Bik-chu Chow, Patrick Ip
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Background Little is known about the progression of obesity from childhood to adolescence. This study aimed to longitudinally examine the obesity status in a cohort of children across their childhood and adolescence, and to identify the fact
Externí odkaz:
https://doaj.org/article/1532d2f3001d42d8955dc8f7ab3d7a9e
Publikováno v:
BMJ case reports. 15(11)
Hyperreactio luteinalis is a benign, pregnancy-related condition with cystic enlargement of the ovaries and elevated androgen. However, only one-third of patients manifest as maternal virilisation and rarely does it cause fetal virilisation. Here, we
Autor:
Ingrid Libman, Aveni Haynes, Sarah Lyons, Praveen Pradeep, Edson Rwagasor, Joanna Yuet‐ling Tung, Craig A. Jefferies, Richard A. Oram, Dana Dabelea, Maria E. Craig
Publikováno v:
Pediatric Diabetes. 23:1160-1174
Publikováno v:
JCEM Case Reports. 1
Congenital lipoid adrenal hyperplasia (CLAH) is a rare cause of adrenal insufficiency caused by mutations in the steroidogenic acute regulatory (StAR) gene. Patients classically present with adrenal crisis in early infancy and female external genital
Publikováno v:
Clinical Pediatric Endocrinology. 31:168-171
Publikováno v:
Journal of Bone and Mineral Metabolism. 39:606-611
Osteoporosis is a major health issue in boys with Duchenne muscular dystrophy (DMD). Data on the specific bone deficits and microarchitectural alterations in children with DMD were limited. This study aimed to assess the bone microarchitectural alter
Autor:
Arupa Ganguly, Joanna Yuet-ling Tung, Diva D. DeLeón, Kelvin Y.K. Chan, Jennifer M. Kalish, Brian H.Y. Chung, Florence Loong, Anita Sik Yau Kan, Kit San Yeung, Sophie Hon Yu Lai, Sandy Leung Kuen Au
Publikováno v:
International Journal of Pediatric Endocrinology, Vol 2020, Iss 1, Pp 1-6 (2020)
International Journal of Pediatric Endocrinology
International Journal of Pediatric Endocrinology
Background Beckwith–Wiedemann syndrome (BWS) is an overgrowth syndrome with variable clinical phenotype and complex molecular aetiology. It is mainly caused by dysregulation of the chromosome 11p15 imprinted region, which results in overgrowth in m