"Osteogenesis Imperfecta" 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.
COLLAGEN DISEASES characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. Most types are autosomal dominant and are associated with mutations in COLLAGEN TYPE I.
| Descriptor ID |
D010013
|
| MeSH Number(s) |
C05.116.099.708.685 C16.320.737 C17.300.200.540
|
| Concept/Terms |
Lobstein's Disease- Lobstein's Disease
- Disease, Lobstein's
- Lobsteins Disease
- Osteogenesis Imperfecta, Type I
- Osteogenesis Imperfecta with Blue Sclerae
- Osteogenesis Imperfecta, Type 1
- Lobstein Disease
- Disease, Lobstein
- Osteogenesis Imperfecta Tarda
- Osteogenesis Imperfecta Tardas
|
Below are MeSH descriptors whose meaning is more general than "Osteogenesis Imperfecta".
Below are MeSH descriptors whose meaning is more specific than "Osteogenesis Imperfecta".
This graph shows the total number of publications written about "Osteogenesis Imperfecta" by people in this website by year, and whether "Osteogenesis Imperfecta" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2014 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 4 | 0 | 4 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Osteogenesis Imperfecta" by people in Profiles.
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Fibrogenesis Imperfecta Ossium. Calcif Tissue Int. 2019 05; 104(5):561-569.
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Application of next-generation sequencing for molecular diagnosis in a large family with osteogenesis imperfecta type I. Mol Med Rep. 2017 Nov; 16(5):6846-6849.
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Combined Spinal-Epidural Anesthesia With Dexmedetomidine-Based Sedation for Multiple Corrective Osteotomies in a Child With Osteogenesis Imperfecta Type III: A Case Report. A A Case Rep. 2017 Jul 15; 9(2):60-63.
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Comparative X-ray morphometry of prenatal osteogenesis imperfecta type 2 and thanatophoric dysplasia: a contribution to prenatal differential diagnosis. Radiol Med. 2017 Nov; 122(11):880-891.
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Osteoporosis-pseudoglioma syndrome: Report of two cases and a manifesting carrier. Ophthalmic Genet. 2017 Sep-Oct; 38(5):473-479.
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Delayed Recognition of Hypopharyngeal Perforation Injury Caused by Transesophageal Echocardiography in a Patient With Osteogenesis Imperfecta. J Cardiothorac Vasc Anesth. 2017 10; 31(5):1724-1727.
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Spontaneous internal carotid artery rupture during neck dissection in osteogenesis imperfecta patient. Auris Nasus Larynx. 2015 Feb; 42(1):56-8.