Male Child with Van Wyk-Grumbach's Syndrome and Other Complications of Long-Standing Primary Hypothyroidism: A Case Report

Author:

Omran Ahmed12,Peng Jing1,Shrestha Biswas3,Ashhab Muhammad Usman1,Yin Fei1

Affiliation:

1. Department of Pediatrics, Xiangya Hospital of Central South University, No. 87 Xiangya Road, Changsha, Hunan 410008, China

2. Department of Pediatrics and Neonatology, Suez Canal University, Ismailia 41522, Egypt

3. Department of Radiology, Third Xiangya Hospital of Central South University, Changsha, Hunan 410008, China

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.

Publisher

Hindawi Limited

Subject

General Medicine

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