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pro vyhledávání: '"Kocher–Debre–Semelaigne syndrome"'
Akademický článek
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Autor:
Manish Gutch, Sukriti Kumar, Annesh Bhattacharjee, Avinash Agarwal, Rao Somendra Singh, Sumit Rungta
Publikováno v:
Journal of the ASEAN Federation of Endocrine Societies, Vol 32, Iss 1 (2017)
Hypothyroidism is a commonly diagnosed endocrine disorder. Typical signs and symptoms of hypothyroidism include lethargy, cold intolerance, hoarseness, dry skin, constipation, delayed relaxation phase of deep tendon reflexes, and bradycardia. However
Externí odkaz:
https://doaj.org/article/50bbeac7fdd640a683bc56ef9e86e549
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Publikováno v:
Online Journal of Health & Allied Sciences, Vol 14, Iss 3 (2015)
Muscular pseudohypertrophy associated with severe congenital hypothyroidism has been described as Kocher Debre Semelaigne syndrome, which is a rare disorder. We report a case of 9year old female child with hypothyroidism, limb muscular pseudo-hypertr
Externí odkaz:
https://doaj.org/article/ac743513b0c14362b82277a8032d7e1e
Autor:
Sunil R. Panat, Prakash Chandra Jha, Sangamesh N. Chinnannavar, Ankkita Chakarvarty, Ashish Aggarwal
Publikováno v:
Oman Medical Journal, Vol 28, Iss 2, Pp 128-130 (2013)
Kocher Debre Semelaigne Syndrome is a rare syndrome with clinical manifestation of hypothyroidism associated with pseudomuscular hypertrophy. Very few cases have been reported on kocher-debre semelaigne syndrome in the literature with the incidence r
Externí odkaz:
https://doaj.org/article/5bd6d11593624f26b51bb022173c24cb
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 6, Pp 1032-1034 (2012)
Kocher-Debre-Semelaigne (KDS) syndrome is a rare form of hypothyroid myopathy, with associated hypertrophy of muscles. Although cardiac manifestations of hypothyroidism are well known, reports of cardiac involvement in KDS have only described the occ
Externí odkaz:
https://doaj.org/article/1d9ef13001a54b65805bd7330250e1d9
Autor:
Deepak Chand Gupta, Abhinav Gupta, Manish Gutch, Syed Mohd Razi, Keshav Kumar Gupta, Syeda Iqra Usman
Publikováno v:
European Thyroid Journal. 6:47-51
Background: Van Wyk-Grumbach syndrome (VWGS) is a rare presentation of juvenile hypothyroidism which manifests in females as chronic autoimmune hypothyroidism, isosexual pseudoprecocious puberty, and multicystic ovaries. It uniquely presents with sho
Autor:
Elena A. Bogova, Tatyana Shiryaeva
Publikováno v:
Problems of Endocrinology. 63:121-123
The Kocher-Debre-Semelaigne syndrome (KDSS) is a rare disease that clinically manifests as hypothyroidism and muscle pseudohypertrophy of the trunk and extremities. KDSS occurs mainly in countries where there is no screening for congenital hypothyroi
Autor:
Shakil Shaikh Resident M, Rajesh Joshi
Publikováno v:
International Journal of Recent Surgical and Medical Sciences, Vol 02, Iss 01, Pp 044-046 (2016)
Van Wyk–Grumbach syndrome (VWGS) is characterized by juvenile hypothyroidism, delayed bone age, and pseudo-precocious puberty. Primary hypothyroidism in the juvenile population generally leads to retardation of linear growth and delayed puberty. Ho
Autor:
Suhair A Othman
The clinical features and management of a 7-year-old boy who presented with Kocher—Debre—Semelaigne syndrome (KDSS) are described. KDSS is a rare complication of the long-standing, untreated congenital hypothyroidism. It can be encountered in cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac895a84d9713b14b74ca66c7f44b2f1
https://europepmc.org/articles/PMC6378584/
https://europepmc.org/articles/PMC6378584/