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Synostosis involving the elbow

MedGen UID:
871030
•Concept ID:
C4025494
•
Anatomical Abnormality
Synonym: Bone fusion involving the elbow
 
HPO: HP:0003938

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVSynostosis involving the elbow

Professional guidelines

PubMed

Operative treatment of post-traumatic proximal radioulnar synostosis.
Jupiter JB, Ring D
J Bone Joint Surg Am 1998 Feb;80(2):248-57. doi: 10.2106/00004623-199802000-00012. PMID: 9486731
The classification and treatment of heterotopic ossification about the elbow and forearm.
Hastings H 2nd, Graham TJ
Hand Clin 1994 Aug;10(3):417-37. PMID: 7962148
Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis.
Cohen MM Jr
Am J Med Genet 1993 Feb 1;45(3):300-7. doi: 10.1002/ajmg.1320450305. PMID: 8434615

Recent clinical studies

Etiology

Double-level Intraperiosteal Derotational Osteotomy for Congenital Radioulnar Synostosis.
Martínez-Álvarez S, González-Codó S, Vara-Patudo I, Galán-Olleros M, Fraga-Collarte M, Palazón-Quevedo Á
J Pediatr Orthop 2022 Aug 1;42(7):e756-e761. Epub 2022 Jun 8 doi: 10.1097/BPO.0000000000002191. PMID: 35671235
Heterotopic ossification formation after fractures about the elbow.
Wahl EP, Casey PM, Risoli T Jr, Green CL, Richard MJ, Ruch DS
Eur J Orthop Surg Traumatol 2021 Aug;31(6):1061-1067. Epub 2021 Jan 2 doi: 10.1007/s00590-020-02855-4. PMID: 33389077
Distal biceps tendon rupture: advantages and drawbacks of the anatomical reinsertion with a modified double incision approach.
Tarallo L, Lombardi M, Zambianchi F, Giorgini A, Catani F
BMC Musculoskelet Disord 2018 Oct 10;19(1):364. doi: 10.1186/s12891-018-2278-1. PMID: 30305070Free PMC Article
Type 0 ulnar longitudinal deficiency.
Havenhill TG, Manske PR, Patel A, Goldfarb CA
J Hand Surg Am 2005 Nov;30(6):1288-93. doi: 10.1016/j.jhsa.2005.07.006. PMID: 16344190
The classification and treatment of heterotopic ossification about the elbow and forearm.
Hastings H 2nd, Graham TJ
Hand Clin 1994 Aug;10(3):417-37. PMID: 7962148

Diagnosis

A novel variant in MAP3K7 associated with an expanded cardiospondylocarpofacial syndrome phenotype.
AbuBakr F, Jeffries L, Ji W, McGrath JM, Lakhani SA
Cold Spring Harb Mol Case Stud 2020 Jun;6(3) Epub 2020 Jun 12 doi: 10.1101/mcs.a005207. PMID: 32299812Free PMC Article
Tarsal-carpal coalition syndrome: importance of early diagnosis.
Lau GTY, Athalye-Jape G, Amery N
BMJ Case Rep 2019 Jun 6;12(6) doi: 10.1136/bcr-2019-229391. PMID: 31175114Free PMC Article
The developmental spectrum of proximal radioulnar synostosis.
Elliott AM, Kibria L, Reed MH
Skeletal Radiol 2010 Jan;39(1):49-54. doi: 10.1007/s00256-009-0762-2. PMID: 19669136
Pfeiffer syndrome.
Vogels A, Fryns JP
Orphanet J Rare Dis 2006 Jun 1;1:19. doi: 10.1186/1750-1172-1-19. PMID: 16740155Free PMC Article
Type 0 ulnar longitudinal deficiency.
Havenhill TG, Manske PR, Patel A, Goldfarb CA
J Hand Surg Am 2005 Nov;30(6):1288-93. doi: 10.1016/j.jhsa.2005.07.006. PMID: 16344190

Therapy

Distal biceps tendon rupture: advantages and drawbacks of the anatomical reinsertion with a modified double incision approach.
Tarallo L, Lombardi M, Zambianchi F, Giorgini A, Catani F
BMC Musculoskelet Disord 2018 Oct 10;19(1):364. doi: 10.1186/s12891-018-2278-1. PMID: 30305070Free PMC Article

Prognosis

Novel FGF9 variant contributes to multiple synostoses syndrome 3.
Dobson SM, Kiss C, Borschneck D, Heath KE, Gross A, Glucksman MJ, Guerin A
Am J Med Genet A 2022 Jul;188(7):2162-2167. Epub 2022 Mar 22 doi: 10.1002/ajmg.a.62729. PMID: 35316564
Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2.
Kantaputra PN, Dejkhamron P, Intachai W, Ngamphiw C, Kawasaki K, Ohazama A, Krisanaprakornkit S, Olsen B, Tongsima S, Ketudat Cairns JR
Eur J Orthod 2021 Jan 29;43(1):45-50. doi: 10.1093/ejo/cjaa023. PMID: 32255174
Ocular anterior chamber dysgenesis in craniosynostosis syndromes with a fibroblast growth factor receptor 2 mutation.
Okajima K, Robinson LK, Hart MA, Abuelo DN, Cowan LS, Hasegawa T, Maumenee IH, Jabs EW
Am J Med Genet 1999 Jul 16;85(2):160-70. doi: 10.1002/(sici)1096-8628(19990716)85:2<160::aid-ajmg11>3.0.co;2-r. PMID: 10406670
Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis.
Cohen MM Jr
Am J Med Genet 1993 Feb 1;45(3):300-7. doi: 10.1002/ajmg.1320450305. PMID: 8434615

Clinical prediction guides

Double-level Intraperiosteal Derotational Osteotomy for Congenital Radioulnar Synostosis.
Martínez-Álvarez S, González-Codó S, Vara-Patudo I, Galán-Olleros M, Fraga-Collarte M, Palazón-Quevedo Á
J Pediatr Orthop 2022 Aug 1;42(7):e756-e761. Epub 2022 Jun 8 doi: 10.1097/BPO.0000000000002191. PMID: 35671235
Novel FGF9 variant contributes to multiple synostoses syndrome 3.
Dobson SM, Kiss C, Borschneck D, Heath KE, Gross A, Glucksman MJ, Guerin A
Am J Med Genet A 2022 Jul;188(7):2162-2167. Epub 2022 Mar 22 doi: 10.1002/ajmg.a.62729. PMID: 35316564
Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2.
Kantaputra PN, Dejkhamron P, Intachai W, Ngamphiw C, Kawasaki K, Ohazama A, Krisanaprakornkit S, Olsen B, Tongsima S, Ketudat Cairns JR
Eur J Orthod 2021 Jan 29;43(1):45-50. doi: 10.1093/ejo/cjaa023. PMID: 32255174
Posterior dislocation of the elbow with fractures of the radial head and coronoid.
Ring D, Jupiter JB, Zilberfarb J
J Bone Joint Surg Am 2002 Apr;84(4):547-51. doi: 10.2106/00004623-200204000-00006. PMID: 11940613
The classification and treatment of heterotopic ossification about the elbow and forearm.
Hastings H 2nd, Graham TJ
Hand Clin 1994 Aug;10(3):417-37. PMID: 7962148

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