"Trisomy 13 Syndrome" 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 chromosome disorder associated with TRISOMY of all or part of CHROMOSOME 13. Clinical manifestations include CONGENITAL HEART DEFECTS (e.g., PATENT DUCTUS ARTERIOSUS), facial malformations (e.g., CLEFT LIP; CLEFT PALATE; COLOBOMA; MICROPHTHALMIA); HYPOTONIA, digit malformations (e.g., POLYDACTYLY or SYNDACTYLY), and SEIZURES and severe INTELLECTUAL DISABILITY associated with NERVOUS SYSTEM MALFORMATIONS.
| Descriptor ID |
D000073839
|
| MeSH Number(s) |
C10.597.606.643.835 C14.240.400.970 C14.280.400.970 C16.131.077.919 C16.131.240.400.965 C16.131.260.923 C16.320.180.923
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| Concept/Terms |
Trisomy 13 Syndrome- Trisomy 13 Syndrome
- Patau's Syndrome
- Pataus Syndrome
- Bartholin-Patau Syndrome
- Bartholin Patau Syndrome
- Chromosome 13 Trisomy Syndrome
- Trisomy 13 Syndromes
- Patau Syndrome
|
Below are MeSH descriptors whose meaning is more general than "Trisomy 13 Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Trisomy 13 Syndrome".
This graph shows the total number of publications written about "Trisomy 13 Syndrome" by people in this website by year, and whether "Trisomy 13 Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 0 | 1 | 1 |
| 2014 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
| 2020 | 0 | 2 | 2 |
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Below are the most recent publications written about "Trisomy 13 Syndrome" by people in Profiles.
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Commentary: Cardiac surgery in children with trisomy 13 and trisomy 18: "Is it the quality of life or the quantity?" J Thorac Cardiovasc Surg. 2021 07; 162(1):251-252.
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Assessment of laboratories offering cell-free (cf) DNA screening for Down syndrome: results of the 2018 College of American Pathology External Educational Exercises. Genet Med. 2020 04; 22(4):777-784.
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Adherence of cell-free DNA noninvasive prenatal screens to ACMG recommendations. Genet Med. 2019 10; 21(10):2285-2292.
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Mortality and morbidity of VLBW infants with trisomy 13 or trisomy 18. Pediatrics. 2014 Feb; 133(2):226-35.
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Major chromosomal anomalies among very low birth weight infants in the Vermont Oxford Network. J Pediatr. 2012 May; 160(5):774-780.e11.