"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
|
| 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.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2013 | 0 | 2 | 2 |
| 2014 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2019 | 0 | 2 | 2 |
| 2020 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Trisomy 13 Syndrome" by people in Profiles.
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Ethical Implications of Cleft Lip and Palate Repair in Patients with Trisomy 13 and Trisomy 18. Cleft Palate Craniofac J. 2024 Aug; 61(8):1383-1388.
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Patterns of congenital anomalies among individuals with trisomy 13 in Texas. Am J Med Genet A. 2021 06; 185(6):1787-1793.
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Outcomes After Extracorporeal Life Support Cannulation in Pediatric Patients With Trisomy 13 and Trisomy 18. J Surg Res. 2021 01; 257:260-266.
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Polydactyly. Am J Obstet Gynecol. 2019 12; 221(6):B13-B15.
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Radial Ray Malformation. Am J Obstet Gynecol. 2019 12; 221(6):B16-B18.
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Clinical application of a contingent screening strategy for trisomies with cell-free DNA: a pilot study. BMC Pregnancy Childbirth. 2019 Aug 01; 19(1):274.
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Survival and healthcare utilization of infants diagnosed with lethal congenital malformations. J Perinatol. 2018 12; 38(12):1674-1684.
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Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory. Am J Obstet Gynecol. 2017 12; 217(6):691.e1-691.e6.
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Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center. Ultrasound Obstet Gynecol. 2014 Mar; 43(3):254-64.
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Hepatoblastoma in a 15-month-old female with trisomy 13. Am J Med Genet A. 2014 Feb; 164A(2):472-5.