 Failure to Thrive
"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
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| MeSH Number(s) |
C23.888.338
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| Concept/Terms |
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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 | | 2017 | 0 | 1 | 1 | | 2018 | 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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Lewis AH, Chugh A, Sobotka SA. 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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Slater BJ, Rothenberg SS. Fundoplication. Clin Perinatol. 2017 12; 44(4):795-803.
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Li MH, Arndt K, Das S, Weiss EM, Wu Y, Gwal K, Shekdar KV, Zackai EH. 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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Niebur H, Akhter J, Balliu E, Boykan R, Chitkara M, Bag-Ozbek A, Kim M, Azzam RK, Hageman J. Index of suspicion. Pediatr Rev. 2014 Feb; 35(2):88-93.
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Raghavan A, Cade-Bell I, Kahn SA, Waggoner DJ, Hageman J. An unusual case of an infant with failure to thrive. Pediatr Ann. 2012 Dec; 41(12):502-5.
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Hehir DA, Rudd N, Slicker J, Mussatto KA, Simpson P, Li SH, Frommelt MA, Tweddell JS, Ghanayem NS. Normal interstage growth after the norwood operation associated with interstage home monitoring. Pediatr Cardiol. 2012 Dec; 33(8):1315-22.
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Shoukier M, Klein N, Auber B, Wickert J, Schröder J, Zoll B, Burfeind P, Bartels I, Alsat EA, Lingen M, Grzmil P, Schulze S, Keyser J, Weise D, Borchers M, Hobbiebrunken E, Röbl M, Gärtner J, Brockmann K, Zirn B. 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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Sakata Y, Kamei CN, Nakagami H, Bronson R, Liao JK, Chin MT. 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.
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Sentongo TA, Markowitz RI, Russo P, vonAllmen D, Piccoli DA. Pathological case of the month. Type IV sacrococcygeal teratoma with yolk sac (endodermal sinus) tumor presenting with failure to thrive and perianal pain. Arch Pediatr Adolesc Med. 2002 Apr; 156(4):405-6.
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Sentongo TA, Tershakovec AM, Mascarenhas MR, Watson MH, Stallings VA. Resting energy expenditure and prediction equations in young children with failure to thrive. J Pediatr. 2000 Mar; 136(3):345-50.
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