"Failure to Thrive" 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 of substandard growth or diminished capacity to maintain normal function.
| Descriptor ID |
D005183
|
| MeSH Number(s) |
C23.888.338
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Failure to Thrive".
Below are MeSH descriptors whose meaning is more specific than "Failure to Thrive".
This graph shows the total number of publications written about "Failure to Thrive" by people in this website by year, and whether "Failure to Thrive" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 0 | 1 | 1 |
| 1998 | 1 | 0 | 1 |
| 2000 | 1 | 0 | 1 |
| 2002 | 1 | 1 | 2 |
| 2012 | 2 | 1 | 3 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Failure to Thrive" by people in Profiles.
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Failure to Thrive in a 2-month-old Boy. Pediatr Rev. 2020 Dec; 41(12):642-644.
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Behavioral Outbursts in a Child with a Deletion Syndrome, Generalized Epilepsy, Global Developmental Delay, and Failure to Thrive. Pediatr Ann. 2018 Mar 01; 47(3):e130-e134.
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Fundoplication. Clin Perinatol. 2017 12; 44(4):795-803.
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The Fate of Radical Cystectomy Patients after Hospital Discharge: Understanding the Black Box of the Pre-readmission Interval. Eur Urol Focus. 2018 09; 4(5):711-717.
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Compound heterozygote CDK5RAP2 mutations in a Guatemalan/Honduran child with autosomal recessive primary microcephaly, failure to thrive and speech delay. Am J Med Genet A. 2015 Jun; 167(6):1414-7.
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Index of suspicion. Pediatr Rev. 2014 Feb; 35(2):88-93.
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An unusual case of an infant with failure to thrive. Pediatr Ann. 2012 Dec; 41(12):502-5.
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Normal interstage growth after the norwood operation associated with interstage home monitoring. Pediatr Cardiol. 2012 Dec; 33(8):1315-22.
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Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants? Clin Genet. 2013 Jan; 83(1):53-65.
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Ventricular septal defect and cardiomyopathy in mice lacking the transcription factor CHF1/Hey2. Proc Natl Acad Sci U S A. 2002 Dec 10; 99(25):16197-202.