Congenital Hypothyroidism
"Congenital Hypothyroidism" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA.
| Descriptor ID |
D003409
|
| MeSH Number(s) |
C05.116.099.343.347 C05.116.132.256 C16.320.240.625 C19.297.155 C19.874.482.281
|
| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Congenital Hypothyroidism".
Below are MeSH descriptors whose meaning is more specific than "Congenital Hypothyroidism".
This graph shows the total number of publications written about "Congenital Hypothyroidism" by people in this website by year, and whether "Congenital Hypothyroidism" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 0 | 1 | 1 |
| 2008 | 1 | 0 | 1 |
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Below are the most recent publications written about "Congenital Hypothyroidism" by people in Profiles.
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CD80, suPAR and nephrotic syndrome in a case of NPHS2 mutation. Nefrologia. 2013; 33(5):727-31.
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Clinical inquiries. What are the causes of elevated TSH in a newborn? J Fam Pract. 2008 Mar; 57(3):185-7.
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Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence. Am J Med Genet. 1994 Jan 01; 49(1):67-73.