Literature DB >> 16596673

Thyroid anomalies in Williams syndrome: investigation of 95 patients.

A Selicorni1, A Fratoni, M A Pavesi, M Bottigelli, E Arnaboldi, D Milani.   

Abstract

Thyroid involvement in Williams syndrome (WS) was recently reported in two small groups of patients, both showing an increased prevalence of elevation of TSH serum concentration; in one of the two reports, 70% of the patients demonstrated a hypoplasia of thyroid gland as well. In our institution, we currently follow a large population of WS patients who periodically undergo a multispecialist clinical evaluation that includes ultrasound evaluation of the thyroid gland, and levels of FT3, FT4, TSH, and anti-thyroid antibodies. Here, we report on the prevalence of thyroid structural and functional anomalies, in a population of 95 WS patients, half of them followed for more than 5 years. Our study confirms the increased incidence of both elevated TSH serum values (37.9% in our sample) and thyroid gland hypoplasia (74.7%). Moreover, we demonstrated that TSH elevation declines with age. For this reason, we suggest that a complete thyroid evaluation be performed in every patient with WS, and that this medical complication should be periodically searched for in follow-up visits.

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Year:  2006        PMID: 16596673     DOI: 10.1002/ajmg.a.31210

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  10 in total

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2.  Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis.

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Review 3.  Heterogeneous phenotype in children affected by non-autoimmune hypothyroidism: an update.

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4.  Using transcription modules to identify expression clusters perturbed in Williams-Beuren syndrome.

Authors:  Charlotte N Henrichsen; Gábor Csárdi; Marie-Thérèse Zabot; Carmela Fusco; Sven Bergmann; Giuseppe Merla; Alexandre Reymond
Journal:  PLoS Comput Biol       Date:  2011-01-20       Impact factor: 4.475

5.  Williams-Beuren Syndrome: A Clinical Study of 55 Brazilian Patients and the Diagnostic Use of MLPA.

Authors:  Rachel Sayuri Honjo; Roberta Lelis Dutra; Erika Arai Furusawa; Evelin Aline Zanardo; Larissa Sampaio de Athayde Costa; Leslie Domenici Kulikowski; Debora Romeo Bertola; Chong Ae Kim
Journal:  Biomed Res Int       Date:  2015-05-18       Impact factor: 3.411

6.  Endocrine dysfunctions in children with Williams-Beuren syndrome.

Authors:  Yoon-Myung Kim; Ja Hyang Cho; Eungu Kang; Gu-Hwan Kim; Eul-Ju Seo; Beom Hee Lee; Jin-Ho Choi; Han-Wook Yoo
Journal:  Ann Pediatr Endocrinol Metab       Date:  2016-03-31

7.  A rare association of central hypothyroidism and adrenal insufficiency in a boy with Williams-Beuren syndrome.

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Review 8.  Hashimoto's Thyroiditis and Graves' Disease in Genetic Syndromes in Pediatric Age.

Authors:  Celeste Casto; Giorgia Pepe; Alessandra Li Pomi; Domenico Corica; Tommaso Aversa; Malgorzata Wasniewska
Journal:  Genes (Basel)       Date:  2021-02-04       Impact factor: 4.096

9.  Coeliac disease and risk for other autoimmune diseases in patients with Williams-Beuren syndrome.

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Journal:  BMC Med Genet       Date:  2014-05-23       Impact factor: 2.103

Review 10.  Autoimmune Thyroid Disease in Specific Genetic Syndromes in Childhood and Adolescence.

Authors:  Eleni Magdalini Kyritsi; Christina Kanaka-Gantenbein
Journal:  Front Endocrinol (Lausanne)       Date:  2020-08-19       Impact factor: 5.555

  10 in total

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