Results 161 to 170 of about 208,465 (197)
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Thyroid dysfunction and developmental anomalies in first degree relatives of children with thyroid dysgenesis

World Journal of Pediatrics, 2015
Familial clustering in patients with permanent congenital hypothyroidism (CH) caused by thyroid dysgenesis (TD) has been reported in developed countries. There is no information on familial TD from developing countries.A total of 312 first degree relatives belonging to 80 families of children with TD (group 1) and 40 families of age-matched normal ...
Lakshminarasimhan, Sindhuja   +4 more
openaire   +2 more sources

[Thyroid dysgenesis in mother and daughter].

Archives francaises de pediatrie, 1978
A case of congenital hypothyroidism with lingual thyroid in a woman and her daughter is presented. The scarcity of familial cases of thyroid malformations leads to discuss the genetic factors involved.
A, Safar, J L, Bacri, D, Got, J C, Job
openaire   +1 more source

Thyroid-stimulating hormone in thyroid dysgenesis

The Journal of Pediatrics, 1967
H E, Kulin   +3 more
openaire   +2 more sources

Molecular determinants of congenital hypothyroidism due to thyroid dysgenesis

2014
Congenital hypothyroidism from thyroid dysgenesis (CHTD) is the most common congenital endocrine disorder with an incidence of 1 in 4,000 live births. CHTD includes multiple abnormalities in thyroid gland development. Among them, the most common diagnostic category is thyroid ectopy (~ 50 % of cases).
openaire   +1 more source

Extra-Thyroid Congenital Abnormalities Associated with Thyroid Dysgenesis in Turkey

2016
A higher frequency of extra-thyroidal congenital malformations (ETCM) has been reported in children with congenital hypothyroidism (CH) compared with the general population. The most commonly reported one, congenital cardiac malformation (CCM), is reported to be in the range of 2-29% which is much higher than in normal population with a prevalence of 0.
Hatun, S.   +6 more
openaire   +1 more source

Subclinical Hashimoto's thyroiditis in gonadal dysgenesis.

Israel journal of medical sciences, 1981
Two patients with gonadal dysgenesis are described. One had X-isochromosome and the other had a 45,X karyotype. They both had Hashimoto's thyroiditis with extremely low levels of thyroid hormones, but no clinical signs or symptoms of hypothyroidism, and no goiter. Even with replacement therapy and restoration of normal thyroid hormone levels, there was
openaire   +1 more source

Diabetes Mellitus and Thyroid Autoimmunity in Gonadal Dysgenesis

Fertility and Sterility, 1973
J, Van Campenhout, A, Antaki, E, Rasio
openaire   +2 more sources

New Developments in the Diagnosis and Treatment of Thyroid Cancer

Ca-A Cancer Journal for Clinicians, 2013
David F Schneider, Herbert Chen
exaly  

The Incidental Thyroid Nodule

Ca-A Cancer Journal for Clinicians, 2018
Sarah B Fisher
exaly  

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