Abstract
Primary hypothyroidism in the juvenile population generally leads to retardation of linear growth and delay or even arrest of puberty. However, in rare conditions, children with long-standing hypothyroidism present with signs of Van Wyk-Grumbach's syndrome (VWGS) which include juvenile hypothyroidism, delayed bone age, and pseudoprecocious puberty. We report a rare case of prepubertal male child from Asian origin, presented with long-standing untreated hypothyroidism complicated with VWGS and other complications including obesity, short stature, hepatomegaly, asymptomatic mild pericardial effusion, and pituitary hyperplasia.
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CITATION STYLE
Omran, A., Peng, J., Shrestha, B., Ashhab, M. U., & Yin, F. (2012). Male Child with Van Wyk-Grumbach’s Syndrome and Other Complications of Long-Standing Primary Hypothyroidism: A Case Report. Case Reports in Pediatrics, 2012, 1–5. https://doi.org/10.1155/2012/352751
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