Thyroid hypoplasia (Q98319): Difference between revisions
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Hipoplasia tireoidiana é uma forma de disgenesia da tireoide caracterizada pelo desenvolvimento incompleto da glândula tireoide que resulta em hipotireoidismo congênito primário, uma deficiência tireoidiana permanente que está presente desde o nascimento. | |||
| description / en | description / en | ||
Thyroid hypoplasia is a form of thyroid dysgenesis characterised by incomplete development of the thyroid gland that results in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. | |||
Revision as of 14:44, 16 August 2026
Thyroid hypoplasia is a form of thyroid dysgenesis characterised by incomplete development of the thyroid gland that results in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_936952450 |
||
| English | Thyroid hypoplasia |
Thyroid hypoplasia is a form of thyroid dysgenesis characterised by incomplete development of the thyroid gland that results in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. |
