Cretinism screening: Difference between revisions
Jump to navigation
Jump to search
Usama Talib (talk | contribs) No edit summary |
|||
| Line 4: | Line 4: | ||
==Overview== | ==Overview== | ||
According to the [guideline name], screening for [disease name] is not recommended. | According to the [guideline name], screening for [disease name] is not recommended. | ||
| Line 15: | Line 11: | ||
According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with [condition 1], [condition 2], and [condition 3]. | According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with [condition 1], [condition 2], and [condition 3]. | ||
==Screening== | ==Screening== | ||
*According to the endocrine society and the European society for pediatric endocrinology, screening for congenital hypothyroidism (cretinism) is recommended in all neonates.<ref name="pmid24446653">{{cite journal| author=Léger J, Olivieri A, Donaldson M, Torresani T, Krude H, van Vliet G et al.| title=European Society for Paediatric Endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism. | journal=J Clin Endocrinol Metab | year= 2014 | volume= 99 | issue= 2 | pages= 363-84 | pmid=24446653 | doi=10.1210/jc.2013-1891 | pmc=4207909 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24446653 }}</ref> | |||
*According to the | |||
OR | OR | ||
*According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with: | *According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with: | ||
Revision as of 19:23, 16 August 2017
|
Cretinism Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Cretinism screening On the Web |
|
American Roentgen Ray Society Images of Cretinism screening |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
According to the [guideline name], screening for [disease name] is not recommended.
OR
According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with [condition 1], [condition 2], and [condition 3].
Screening
- According to the endocrine society and the European society for pediatric endocrinology, screening for congenital hypothyroidism (cretinism) is recommended in all neonates.[1]
OR
- According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with:
- [condition 1]
- [condition 2]
- [condition 3]
References
- ↑ Léger J, Olivieri A, Donaldson M, Torresani T, Krude H, van Vliet G; et al. (2014). "European Society for Paediatric Endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism". J Clin Endocrinol Metab. 99 (2): 363–84. doi:10.1210/jc.2013-1891. PMC 4207909. PMID 24446653.