 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
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| MeSH Number(s) |
C05.116.099
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| 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
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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 |
|---|
| 2007 | 1 | 0 | 1 | | 2013 | 2 | 0 | 2 | | 2017 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 | | 2019 | 2 | 0 | 2 | | 2022 | 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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Gracie S, Sengupta N, Ferreira C, Pemberton J, Anderson I, Wang X, Rhodes L, Brown K, Balla T, Larson A. De novo loss-of-function variant in PTDSS1 is associated with developmental delay. Am J Med Genet A. 2022 06; 188(6):1739-1745.
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Helenius IJ, Saarinen AJ, White KK, McClung A, Yazici M, Garg S, Thompson GH, Johnston CE, Pahys JM, Vitale MG, Akbarnia BA, Sponseller PD. Results of growth-friendly management of early-onset scoliosis in children with and without skeletal dysplasias: a matched comparison. Bone Joint J. 2019 12; 101-B(12):1563-1569.
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O'Donnell C, Garg S. Comment on: Slipped capital femoral epiphysis and Blount's disease as indicators for early metabolic surgical intervention. Surg Obes Relat Dis. 2019 10; 15(10):1842-1843.
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White KK, Bompadre V, Shah SA, Redding GJ, Krengel WF, Mackenzie WG. Early-Onset Spinal Deformity in Skeletal Dysplasias: A Multicenter Study of Growth-Friendly Systems. Spine Deform. 2018 Jul - Aug; 6(4):478-482.
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Zarate YA, Steinraths M, Matthews A, Smith WE, Sun A, Wilson LC, Brain C, Allgove J, Jacobs B, Fish JL, Powell CM, Wasserman WW, van Karnebeek CD, Wakeling EL, Ma NS. Bone health and SATB2-associated syndrome. Clin Genet. 2018 03; 93(3):588-594.
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Gray MJ, Kannu P, Sharma S, Neyt C, Zhang D, Paria N, Daniel PB, Whetstone H, Sprenger HG, Hammerschmidt P, Weng A, Dupuis L, Jobling R, Mendoza-Londono R, Dray M, Su P, Wilson MJ, Kapur RP, McCarthy EF, Alman BA, Howard A, Somers GR, Marshall CR, Manners S, Flanagan AM, Rathjen KE, Karol LA, Crawford H, Markie DM, Rios JJ, Wise CA, Robertson SP. Mutations Preventing Regulated Exon Skipping in MET Cause Osteofibrous Dysplasia. Am J Hum Genet. 2015 Dec 03; 97(6):837-47.
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Johnston PS, Paxton ES, Gordon V, Kraeutler MJ, Abboud JA, Williams GR. Os acromiale: a review and an introduction of a new surgical technique for management. Orthop Clin North Am. 2013 Oct; 44(4):635-44.
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Kochhar A, Kirmani S, Cetta F, Younge B, Hyland JC, Michels V. Similarity of geleophysic dysplasia and Weill-Marchesani syndrome. Am J Med Genet A. 2013 Dec; 161A(12):3130-2.
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Braman JP, Stewart TM. Treatment of proximal humeral dysplasia epiphysealis hemimelica with custom hemiarthroplasty: a case report. J Shoulder Elbow Surg. 2011 Dec; 20(8):e1-3.
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Beales PL, Bland E, Tobin JL, Bacchelli C, Tuysuz B, Hill J, Rix S, Pearson CG, Kai M, Hartley J, Johnson C, Irving M, Elcioglu N, Winey M, Tada M, Scambler PJ. IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy. Nat Genet. 2007 Jun; 39(6):727-9.
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