Zobrazeno 1 - 10
of 369
pro vyhledávání: '"hemiagenesis"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 17, Iss 12, Pp 01-03 (2023)
Thyroid Hemiagenesis (TH) is a rare condition characterised by developmental abnormalities of the thyroid, often observed on the left-side, with a higher prevalence in females. It is commonly associated with a lack of the isthmus. A seven-year-old bo
Externí odkaz:
https://doaj.org/article/0b0bb53b676e46c2aee820136ea4974b
Publikováno v:
Journal of Clinical and Translational Endocrinology Case Reports, Vol 30, Iss , Pp 100134- (2023)
Background: Thyroid hemiagenesis (TH) is a rare disorder that is usually clinically silent unless associated with other thyroidal pathologies. We present a case of a TH patient with Graves’ disease (GD). To our knowledge, this is the first ever cas
Externí odkaz:
https://doaj.org/article/1e8b0c82d7494f16bbd60ef03ecd7fbb
Autor:
Dae Young Yoon, Eun Soo Kim, Chae Woon Lee, Young Lan Seo, Yul Lee, Mi Jung Kwon, Sang Min Lee
Publikováno v:
BMC Medical Imaging, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Objectives Thyroid hemiagenesis is a rare congenital anomaly characterized by the lack of development of one thyroid lobe. The purpose of this study was to evaluate computed tomography (CT) findings of thyroid hemiagenesis and to establish u
Externí odkaz:
https://doaj.org/article/b283d351ff6e419688391464d4e01606
Publikováno v:
Asian Journal of Surgery, Vol 46, Iss 10, Pp 4545-4546 (2023)
Externí odkaz:
https://doaj.org/article/7b75900489c4402aac82d600391353e1
Publikováno v:
Acta Oto-Laryngologica Case Reports, Vol 6, Iss 1, Pp 91-95 (2021)
Concurrent thyroid hemiagenesis and ectopic thyroid tissue are rare conditions and can challenge the clinical appearance. Only one other case story in the literature has described thyroid hemiagenesis and concurrent submandibular ectopic thyroid tiss
Externí odkaz:
https://doaj.org/article/38a81ed5701541c69b58bb5261a02a8e
Publikováno v:
Journal of Clinical and Translational Endocrinology Case Reports, Vol 26, Iss , Pp 100128- (2022)
Background: Thyroid hemiagenesis (TH) is a rare disorder that is usually clinically silent unless associated with other thyroidal pathologies. We present a case of a TH patient with Graves' disease (GD). To our knowledge, this is the first ever case
Externí odkaz:
https://doaj.org/article/9df34948290f40e696cb487a134d8172
Akademický článek
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Publikováno v:
Thyroid Research, Vol 14, Iss 1, Pp 1-4 (2021)
Abstract Background Thyroid hemiagenesis is a rare congenital anomaly in which one lobe of the thyroid gland fails to develop. There is an increased incidence of associated thyroid disorders in patients with thyroid hemiagenesis. Case presentation A
Externí odkaz:
https://doaj.org/article/e771c68431b04593bccb1a73e201acef
Publikováno v:
Clinical Case Reports, Vol 9, Iss 3, Pp 1615-1620 (2021)
Abstract The combination of TH and PHPT or PTC is extremely rare. A better comprehension of the normal anatomy of the thyroid gland and its variations, congenital anomalies, and related pathologies is essential for safe surgical intervention.
Externí odkaz:
https://doaj.org/article/dc027539801242629202239d1e7e9287
Autor:
Ewelina Szczepanek-Parulska, Bartłomiej Budny, Martyna Borowczyk, Igor Zhukov, Kosma Szutkowski, Katarzyna Zawadzka, Raiha Tahir, Andrzej Minczykowski, Marek Niedziela, Marek Ruchała
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 6, p 3414 (2022)
Thyroid hemiagenesis (THA) is an inborn absence of one thyroid lobe of largely unknown etiopathogenesis. The aim of the study was to reveal genetic factors responsible for thyroid maldevelopment in two siblings with THA. None of the family members pr
Externí odkaz:
https://doaj.org/article/0181dc0f7607407d97f37b067675032c