Congenital Hypothyroidism Due to Dyshormonogenesis in 2 Siblings
Author:
Funder
Indian Council of Medical Research
Fetal Care Research Foundation
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/article/10.1007/s12098-017-2516-9/fulltext.html
Reference4 articles.
1. Sparling DP, Fabian K, Harik L, et al. Congenital hypothyroidism and thyroid dyshormonogenesis: a case report of siblings with a newly identified mutation in thyroperoxidase. J Pediatr Endocrinol Metab. 2016;29:627–31.
2. Ramesh BG, Bhargav PR, Rajesh BG, Devi NV, Vijayaraghavan R, Varma BA. Genotype-phenotype correlations of dyshormonogenetic goiter in children and adolescents from South India. Indian J Endocrinol Metab. 2016;20:816–24.
3. Rastogi MV, LaFranchi SH. Congenital hypothyroidism. Orph J Rare Dis. 2010;5:17.
4. Castanet M, Lyonnet S, Bonaïti-Pellié C, Polak M, Czernichow P, Léger J. Familial forms of thyroid dysgenesis among infants with congenital hypothyroidism. New Engl J Med. 2000;343:441–2.
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