Thyroid dysfunction in Indian children with down syndrome

2014 ◽  
Vol 51 (9) ◽  
pp. 751-753 ◽  
Author(s):  
Devi Dayal ◽  
Puneet Jain ◽  
Inusha Panigrahi ◽  
Anish Bhattacharya ◽  
Naresh Sachdeva ◽  
...  
Author(s):  
Mandula Phani Priya ◽  
Neerja Gupta ◽  
Aditya Nagori ◽  
Rakesh Lodha ◽  
Vandana Jain ◽  
...  

1977 ◽  
Vol 35 (1) ◽  
pp. 1-5 ◽  
Author(s):  
Benjamin J. Schmidt ◽  
Nelson Carvalho ◽  
Stanislau Krynski ◽  
Cláudio C. Ortega ◽  
José Liberman ◽  
...  

Serum TSH was studied in 22 patients with Down syndrome, from 4 to 15 years old. In 6 of these patients radioiodine uptake by thyroid gland after 2 and 24 hours of administration and clearance rates before and after TSH stimulus (10 µl-IM) were measured. Results show that serum TSH was normal in 17 patients and above normal limits in 5 patients. Thyroid uptake after 2 hours as well clearance rates, both below normal, had a response to TSH stimulus with normal or below values. These data along with previous reports, suggest, that in children with Down syndrome, there is a thyroid dysfunction in which a slow response no TSH stimulus seems to be the basic defect.


2020 ◽  
Vol 23 (6) ◽  
pp. 386-390
Author(s):  
Beata Zelazowska-Rutkowska ◽  
Anna Jakubiuk-Tomaszuk ◽  
Bogdan Cylwik

Background: Patients with subclinical thyroid disease have few or no clinical symptoms of thyroid dysfunction and thus, laboratory diagnosis is needed. In this context, the objective of the current study was to analyze the prevalence rate and pattern of thyroid function in children with Down syndrome in the Polish population. Methods: A total of 30 children, aged 6–12 years, with cytogenetically confirmed Down syndrome were studied. The control group included 27 children. Results: Of the 30 patients with Down syndrome, 14 (46.7%) had abnormal thyroid profiles. Mean thyroid-stimulating hormone (TSH) and fT4 concentrations in children with Down syndrome were found to be significantly increased compared with the controls (4.30 ± 1.9 µIU/mL, 95% CI: 3.55–5.04 µIU/mL vs. 3.10 ± 1.47 µIU/mL, 95% CI: 2.52–3.68 µIU/mL, P = 0.013, 95% CI: 0.26–2.14, and 1.33 ± 0.23 ng/dL, 95% CI: 1.25–1.42 vs. 1.19 ± 0.14 ng/dL, 95% CI: 1.13–1.25, P = 0.008, 95% CI: 0.04–0.24, respectively). In Down syndrome, subclinical hypothyroidism was recognized in 10 children (33.3%) (high TSH and normal fT4 and fT3 levels). Two children (6.67%) had evident hypothyroidism (high TSH and low fT4). In the control group, subclinical hypothyroidism was diagnosed in four (14.8%) children. Conclusion: Children with Down syndrome may have increased secretion of TSH, even when thyroid hormone and autoantibodies are normal, suggesting that an isolated increase in TSH does not predispose the patient to the development of thyroid disease. We also recommend that all patients with Down syndrome should be screened for thyroid dysgenesis, since they have thyroid dysfunction more frequently as compared to the general healthy population.


2018 ◽  
Vol 22 (1) ◽  
pp. 6-9
Author(s):  
Vidhya Vishwanathan ◽  
Subramanian Sethuraman ◽  
Shanthi Balaji ◽  
VS Kalai Selvi ◽  
AJ Manjula Devi

1994 ◽  
Vol 14 (4) ◽  
pp. 283-285 ◽  
Author(s):  
Mohamed Ahmed Abdullah ◽  
Hussain Salman ◽  
Sulaiman Al-Habib ◽  
Abdulrahman Ghareeb ◽  
Ahmed Abanamy

2021 ◽  
Vol 11 (3) ◽  
pp. 191-196
Author(s):  
Fahmida Zabeen ◽  
Fauzia Mohsin ◽  
Eva Jesmin ◽  
Sharmin Mahbuba ◽  
M Quamrul Hassan

Background: Down syndrome or trisomy 21 is one of the most common chromosomal disorders with moderate intellectual disability. In addition to mental retardation, this syndrome is associated with different congenital anomalies and characteristic dysmorphic features. Affected individuals are more susceptible to congenital heart disease and digestive anomalies, pulmonary complications, immune and endocrine system disorders. While several international studies have shown association of co-morbidities with trisomy 21, there is insufficient data available in Bangladesh.The present study aimed to evaluate the associated co-morbidities in children with Down syndrome. Methods: A cross-sectional study was conducted among pediatric cases with Down syndrome who attended the endocrine outpatient department (OPD) of BIRDEM General Hospital from June 2006 to December 2016. The cases were diagnosed either by Karyotyping or by characteristic phenotypes.The clinical and laboratory data of the patients were collected from outpatient history records for analysis. Results: There were total 42 children with Down syndrome, with mean age 4.2 years at assessment and female predominance (1.47:1). Thyroid dysfunction was the most common (69%) followed by congenital heart disease (57%). Among the thyroid disorders, acquired hypothyroidism was found in 55% cases, congenital hypothyroidism in 41% cases and only one had hyperthyroidism. Isolated patent ductus arteriosus (PDA) and atrial septal defect (ASD) comprised the commonest single congenital heart disease found in 53% and combined atrioventricular septal defect was the commonest among complex congenital cardiac defect observed in our study. Both thyroid dysfunction and congenital heart disease were found more in female children with Down syndrome than their male counterpart and it was found statistically significant. Fifty percent of our Down syndrome cases were referred from other healthcare centers to address developmental delay. Conclusion: Hypothyroidism and congenital heart disease are frequently associated in Down syndrome children in Bangladesh. This calls for developing awareness among health professionals to diagnose comorbidities at an early stage and to form recommendations for long term follow up. BIRDEM Med J 2021; 11(3): 191-196


2019 ◽  
Vol 44 (8) ◽  
pp. 901-907 ◽  
Author(s):  
Shwetha Mangalesh ◽  
Anand Vinekar ◽  
Chaitra Jayadev ◽  
Vasudha Kemmanu ◽  
Meenakshi Bhat ◽  
...  

2013 ◽  
Vol 103 (12) ◽  
pp. 966 ◽  
Author(s):  
Shahida Moosa ◽  
David G Segal ◽  
Arnold L Christianson ◽  
Nerine E Gregersen

2012 ◽  
Vol 80 (2) ◽  
pp. 114-117 ◽  
Author(s):  
Abdus Sami Bhat ◽  
Mona K. Chaturvedi ◽  
Savita Saini ◽  
Shinjini Bhatnagar ◽  
Neerja Gupta ◽  
...  

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