"Ectromelia" 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.
Gross hypo- or aplasia of one or more long bones of one or more limbs. The concept includes amelia, hemimelia, phocomelia, and sirenomelia.
Descriptor ID |
D004480
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MeSH Number(s) |
C05.660.585.350 C16.131.621.585.350
|
Concept/Terms |
Sirenomelia- Sirenomelia
- Mermaid Malformation
- Malformation, Mermaid
- Sirenomelus
- Sirenomelia Sequence
- Sequence, Sirenomelia
- Sirenomelia Sequences
- Fused Legs and Feet
- Mermaid Syndrome
- Syndrome, Mermaid
|
Below are MeSH descriptors whose meaning is more general than "Ectromelia".
Below are MeSH descriptors whose meaning is more specific than "Ectromelia".
This graph shows the total number of publications written about "Ectromelia" by people in this website by year, and whether "Ectromelia" 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 |
---|
2008 | 0 | 1 | 1 |
2015 | 1 | 0 | 1 |
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Below are the most recent publications written about "Ectromelia" by people in Profiles.
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Neurocognitive profile of a young adolescent with DK phocomelia/von Voss phocomelia/von Voss Cherstvoy syndrome. Am J Med Genet A. 2015 Jul; 167(7):1632-6.
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Hypereosinophilic syndrome and hemimelia in a patient with chromosome 6p22.3 deletion. Pediatr Allergy Immunol. 2014 Aug; 25(5):500-3.
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The non-redundant function of cohesin acetyltransferase Esco2: some answers and new questions. Nucleus. 2012 Jul 01; 3(4):330-4.
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Esco2 promotes neuronal differentiation by repressing Notch signaling. Cell Signal. 2011 Nov; 23(11):1876-84.
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Robinow syndrome: phenotypic variability in a family with a novel intragenic ROR2 mutation. Am J Med Genet A. 2008 Nov 01; 146A(21):2804-9.
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Sirenomelia in an identical twin: a case report. J Pediatr Surg. 1991 Nov; 26(11):1334-6.