"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.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 2 | 3 |
| 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Trisomy 13 Syndrome" by people in Profiles.
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Neonates With Complex Cardiac Malformation and Congenital Diaphragmatic Hernia Born to SARS-CoV-2 Positive Women-A Single Center Experience. World J Pediatr Congenit Heart Surg. 2020 11; 11(6):697-703.
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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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Cell-free fetal DNA analysis in maternal plasma as screening test for trisomies 21, 18 and 13 in twin pregnancy. Ultrasound Obstet Gynecol. 2018 Sep; 52(3):318-324.
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Re: Low-molecular-weight heparin associated with reduced fetal fraction and subsequent false- negative cell-free DNA test result for trisomy 21. Ultrasound Obstet Gynecol. 2018 02; 51(2):278.
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Treatment Decisions for Babies with Trisomy 13 and 18. HEC Forum. 2017 Sep; 29(3):213-222.
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The influence of low molecular weight heparin medication on plasma DNA in pregnant women. Prenat Diagn. 2015 Nov; 35(11):1155-7.