PedAM
Pediatric Disease Annotations & Medicines
| Disease | congenital hypothyroidism |
| Phenotype | C0018021|goiter |
| Sentences | 6 |
| PubMedID- 26478542 | Background: a case of congenital hypothyroidism with goiter (chg) in a juvenile french bulldog was identified and hypothesized to be caused by dyshormonogenesis of genetic etiology. |
| PubMedID- 23737781 | congenital hypothyroidism (ch) with multinodular goiter (mng) is uncommonly seen in children. |
| PubMedID- 21565790 | Context: congenital hypothyroidism (ch) associated with goiter or a gland of normal size has been linked to dual oxidase 2 (duox2) mutations in the presence of iodide organification defect. |
| PubMedID- 23113744 | Background: a cluster of cases of congenital hypothyroidism with goiter (chg) in tenterfield terriers was identified and hypothesized to be dyshormonogenesis of genetic etiology with autosomal recessive inheritance. |
| PubMedID- 22336364 | Method: five patients who had transit congenital hypothyroidism with goiter were enrolled. |
| PubMedID- 23223904 | congenital hypothyroidism with goiter (chg) occurring as an autosomal recessive disorder is typically due to a defect of thyroid hormone synthesis (aka dyshormonogenesis). |
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