Bone Diseases, Developmental
"Bone Diseases, Developmental" 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.
Diseases resulting in abnormal GROWTH or abnormal MORPHOGENESIS of BONES.
| Descriptor ID |
D001848
|
| MeSH Number(s) |
C05.116.099
|
| Concept/Terms |
Bone Diseases, Developmental- Bone Diseases, Developmental
- Bone Dysplasias
- Bone Dysplasia
- Dysplasia, Bone
- Dysplasias, Bone
- Developmental Bone Disease
- Bone Disease, Developmental
- Developmental Bone Diseases
|
Below are MeSH descriptors whose meaning is more general than "Bone Diseases, Developmental".
Below are MeSH descriptors whose meaning is more specific than "Bone Diseases, Developmental".
This graph shows the total number of publications written about "Bone Diseases, Developmental" by people in this website by year, and whether "Bone Diseases, Developmental" 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 |
|---|
| 1999 | 0 | 1 | 1 |
| 2000 | 3 | 0 | 3 |
| 2001 | 1 | 1 | 2 |
| 2005 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
| 2007 | 2 | 0 | 2 |
| 2009 | 1 | 1 | 2 |
| 2010 | 2 | 0 | 2 |
| 2011 | 1 | 0 | 1 |
| 2012 | 0 | 1 | 1 |
| 2013 | 1 | 0 | 1 |
| 2014 | 2 | 1 | 3 |
| 2016 | 1 | 1 | 2 |
| 2017 | 2 | 1 | 3 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 1 | 2 |
| 2020 | 0 | 1 | 1 |
| 2021 | 1 | 0 | 1 |
| 2022 | 0 | 1 | 1 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Bone Diseases, Developmental" by people in Profiles.
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Neuroprotection is improved by watertightness of fetal spina bifida repair in the sheep model. Ultrasound Obstet Gynecol. 2023 01; 61(1):81-92.
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Exacerbation of mild lung disorders to lethal pulmonary hypoplasia by a noncoding hypomorphic SNV in a lung-specific enhancer in trans to the frameshifting TBX4 variant. Am J Med Genet A. 2022 05; 188(5):1420-1425.
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Osteofibrous dysplasia and adamantinoma: A summary of diagnostic challenges and surgical techniques. Surg Oncol. 2021 Sep; 38:101626.
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Ultrasound Evaluation of Pediatric Orthopaedic Patients. J Am Acad Orthop Surg. 2020 Aug 15; 28(16):e696-e705.
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Congenital talipes equinovarus (clubfoot). Am J Obstet Gynecol. 2019 12; 221(6):B10-B12.
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Skin fibroblasts of patients with geleophysic dysplasia due to FBN1 mutations have lysosomal inclusions and losartan improves their microfibril deposition defect. Mol Genet Genomic Med. 2019 09; 7(9):e844.
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Neuroimaging findings of extensive sphenoethmoidal dysplasia in NF1. Clin Imaging. 2018 Sep - Oct; 51:160-163.
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Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with "Corner Fractures". Am J Hum Genet. 2017 Nov 02; 101(5):815-823.
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Haploinsufficiency for ANKRD11-flanking genes makes the difference between KBG and 16q24.3 microdeletion syndromes: 12 new cases. Eur J Hum Genet. 2017 06; 25(6):694-701.
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Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations. Nat Genet. 2017 Apr; 49(4):613-617.