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Page 1
Hearing Loss in Adults: Differential Diagnosis and Treatment.
Michels TC, Duffy MT, Rogers DJ. Michels TC, et al. Am Fam Physician. 2019 Jul 15;100(2):98-108. Am Fam Physician. 2019. PMID: 31305044 Free article. Review.
Patients should then undergo examination for cerumen impaction, exostoses, and other abnormalities of the external canal and tympanic membrane, in addition to a neurologic examination. ...
Patients should then undergo examination for cerumen impaction, exostoses, and other abnormalities of the external canal and tympanic …
Clinical Practice Guideline (Update): Earwax (Cerumen Impaction).
Schwartz SR, Magit AE, Rosenfeld RM, Ballachanda BB, Hackell JM, Krouse HJ, Lawlor CM, Lin K, Parham K, Stutz DR, Walsh S, Woodson EA, Yanagisawa K, Cunningham ER Jr. Schwartz SR, et al. Otolaryngol Head Neck Surg. 2017 Jan;156(1_suppl):S1-S29. doi: 10.1177/0194599816671491. Otolaryngol Head Neck Surg. 2017. PMID: 28045591
The guideline does not apply to patients with cerumen impaction associated with the following conditions: dermatologic diseases of the ear canal; recurrent otitis externa; keratosis obturans; prior radiation therapy affecting the ear; previous tympanoplasty/myringoplasty, …
The guideline does not apply to patients with cerumen impaction associated with the following conditions: dermatologic diseases of the ear c …
A genotype-phenotype study of hereditary multiple exostoses in forty-six Chinese patients.
Li Y, Wang J, Wang Z, Tang J, Yu T. Li Y, et al. BMC Med Genet. 2017 Nov 10;18(1):126. doi: 10.1186/s12881-017-0488-2. BMC Med Genet. 2017. PMID: 29126381 Free PMC article.
BACKGROUND: Hereditary multiple exostoses (HME) is a rare autosomal dominant skeletal disorder that can cause a variety of clinical manifestations. ...
BACKGROUND: Hereditary multiple exostoses (HME) is a rare autosomal dominant skeletal disorder that can cause a variety of clinical m …
Clinical practice guideline: cerumen impaction.
Roland PS, Smith TL, Schwartz SR, Rosenfeld RM, Ballachanda B, Earll JM, Fayad J, Harlor AD Jr, Hirsch BE, Jones SS, Krouse HJ, Magit A, Nelson C, Stutz DR, Wetmore S. Roland PS, et al. Otolaryngol Head Neck Surg. 2008 Sep;139(3 Suppl 2):S1-S21. doi: 10.1016/j.otohns.2008.06.026. Otolaryngol Head Neck Surg. 2008. PMID: 18707628
PURPOSE: The primary purpose of this guideline is to improve diagnostic accuracy for cerumen impaction, promote appropriate intervention in patients with cerumen impaction, highlight the need for evaluation and intervention in special populations, promote appropriate therapeut …
PURPOSE: The primary purpose of this guideline is to improve diagnostic accuracy for cerumen impaction, promote appropriate intervention in …
Nonoperative management of retrocalcaneal pain with AFO and stretching regimen.
Johnson MD, Alvarez RG. Johnson MD, et al. Foot Ankle Int. 2012 Jul;33(7):571-81. doi: 10.3113/FAI.2012.0571. Foot Ankle Int. 2012. PMID: 22835395
Patients with an exostosis less than 1 cm had less improvement than those with an exostosis of 1 cm or more. Patients with Types I and III exostoses had significantly less improvement in FFI compared to Types II and IV. ...CONCLUSION: Our study is the first to report the o …
Patients with an exostosis less than 1 cm had less improvement than those with an exostosis of 1 cm or more. Patients with Types I and III …
Clinical outcome and genotype in patients with hereditary multiple exostoses.
Jäger M, Westhoff B, Portier S, Leube B, Hardt K, Royer-Pokora B, Gossheger G, Krauspe R. Jäger M, et al. J Orthop Res. 2007 Dec;25(12):1541-51. doi: 10.1002/jor.20479. J Orthop Res. 2007. PMID: 17676624 Free article.
Hereditary multiple exostoses (HME) is an autosomal dominant skeletal disorder with a wide spectrum of clinical manifestations. ...were more severely affected, underwent more surgeries, and showed a higher number of exostoses at follow-up. Moreover, we found an incr …
Hereditary multiple exostoses (HME) is an autosomal dominant skeletal disorder with a wide spectrum of clinical manifestations. ...we …
Surgical treatment of nail bed subungual exostosis.
Malkoc M, Korkmaz O, Keskinbora M, Seker A, Oltulu I, Bulbul AM, Say F, Cakir A. Malkoc M, et al. Singapore Med J. 2016 Nov;57(11):630-633. doi: 10.11622/smedj.2015180. Epub 2015 Dec 14. Singapore Med J. 2016. PMID: 26778465 Free PMC article.
INTRODUCTION: A subungual exostosis (SE) is a bony overgrowth that is permanently attached to the tip of the distal phalanx. Its pathology differs from osteocartilaginous exostoses in that it mainly involves the overgrowth of normal bone, which may present beneath the toen …
INTRODUCTION: A subungual exostosis (SE) is a bony overgrowth that is permanently attached to the tip of the distal phalanx. Its pathology d …
Surgical Treatment of Solitary Periarticular Osteochondromas About the Knee in Pediatric and Adolescent Patients: Complications and Functional Outcomes.
Wu M, Zheng ET, Anderson ME, Miller PE, Spencer SA, Heyworth BE. Wu M, et al. J Bone Joint Surg Am. 2021 Jul 21;103(14):1276-1283. doi: 10.2106/JBJS.20.00998. J Bone Joint Surg Am. 2021. PMID: 34029267
BACKGROUND: Solitary osteochondromas, or osteocartilaginous exostoses (OCEs), represent the most common benign bone tumor. Despite frequently causing symptoms about the knee in younger populations, there is minimal previous literature investigating surgical treatment. ...R …
BACKGROUND: Solitary osteochondromas, or osteocartilaginous exostoses (OCEs), represent the most common benign bone tumor. Despite fr …
Hereditary multiple exostoses: anatomical distribution and burden of exostoses is dependent upon genotype and gender.
Clement ND, Porter DE. Clement ND, et al. Scott Med J. 2014 Feb;59(1):35-44. doi: 10.1177/0036933013518150. Epub 2014 Jan 10. Scott Med J. 2014. PMID: 24413927
BACKGROUND AND AIMS: We describe the novel anatomical distribution of exostoses in patients with hereditary multiple exostoses according to their gender and genotype. ...The hand was affected by the greatest proportion of exostoses for both EXT1 (19%) and EXT …
BACKGROUND AND AIMS: We describe the novel anatomical distribution of exostoses in patients with hereditary multiple exostoses …
Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome.
Maas SM, Shaw AC, Bikker H, Lüdecke HJ, van der Tuin K, Badura-Stronka M, Belligni E, Biamino E, Bonati MT, Carvalho DR, Cobben J, de Man SA, Den Hollander NS, Di Donato N, Garavelli L, Grønborg S, Herkert JC, Hoogeboom AJ, Jamsheer A, Latos-Bielenska A, Maat-Kievit A, Magnani C, Marcelis C, Mathijssen IB, Nielsen M, Otten E, Ousager LB, Pilch J, Plomp A, Poke G, Poluha A, Posmyk R, Rieubland C, Silengo M, Simon M, Steichen E, Stumpel C, Szakszon K, Polonkai E, van den Ende J, van der Steen A, van Essen T, van Haeringen A, van Hagen JM, Verheij JB, Mannens MM, Hennekam RC. Maas SM, et al. Eur J Med Genet. 2015 May;58(5):279-92. doi: 10.1016/j.ejmg.2015.03.002. Epub 2015 Mar 16. Eur J Med Genet. 2015. PMID: 25792522
The radiological hallmark are the cone-shaped epiphyses and in TRPS II multiple exostoses. Osteopenia is common in both, as is reduced linear growth, both prenatally and postnatally. ...
The radiological hallmark are the cone-shaped epiphyses and in TRPS II multiple exostoses. Osteopenia is common in both, as is reduce …
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