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11,989 results

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Quoted phrase not found in phrase index: "Sensorineural hearing loss disorder"
Page 1
Contemporary review of the causes and differential diagnosis of sudden sensorineural hearing loss.
Young YH. Young YH. Int J Audiol. 2020 Apr;59(4):243-253. doi: 10.1080/14992027.2019.1689432. Epub 2019 Nov 12. Int J Audiol. 2020. PMID: 31714154 Review.
Objectives: This article provides an overview of the causes and differential diagnosis of sudden deafness (SD) and sudden sensorineural hearing loss (SSHL).Design: Contemporary review.Study sample: This review is based on peer-reviewed articles published in t …
Objectives: This article provides an overview of the causes and differential diagnosis of sudden deafness (SD) and sudden sensorineural …
Harboyan Syndrome.
Javaid A, Orakzai AA. Javaid A, et al. J Ayub Med Coll Abbottabad. 2020 Oct-Dec;32(Suppl 1)(4):S701-S703. J Ayub Med Coll Abbottabad. 2020. PMID: 33754535 Free article.
Harboyan syndrome is a degenerative corneal disorder characterized by congenital hereditary endothelial dystrophy along with progressive, post lingual sensorineural hearing loss. We present the case of a 16-year-old female, who came to us for her follo …
Harboyan syndrome is a degenerative corneal disorder characterized by congenital hereditary endothelial dystrophy along with progress …
MEGDEL Syndrome.
Finsterer J, Scorza FA, Fiorini AC, Scorza CA. Finsterer J, et al. Pediatr Neurol. 2020 Sep;110:25-29. doi: 10.1016/j.pediatrneurol.2020.03.009. Epub 2020 Jul 16. Pediatr Neurol. 2020. PMID: 32684373 Review.
MEGDEL syndrome is an autosomal recessive disorder, clinically characterized by 3-methylglutaconic aciduria, psychomotor delay, muscle hypotonia, sensorineural deafness, and Leigh-like lesions on brain magnetic resonance imaging. ...
MEGDEL syndrome is an autosomal recessive disorder, clinically characterized by 3-methylglutaconic aciduria, psychomotor delay, muscl …
MYH9 Associated nephropathy.
Furlano M, Arlandis R, Venegas MDP, Novelli S, Crespi J, Bullich G, Ayasreh N, Remacha Á, Ruiz P, Lorente L, Ballarín J, Matamala A, Ars E, Torra R. Furlano M, et al. Nefrologia (Engl Ed). 2019 Mar-Apr;39(2):133-140. doi: 10.1016/j.nefro.2018.08.008. Epub 2018 Nov 22. Nefrologia (Engl Ed). 2019. PMID: 30471777 Free article. Review. English, Spanish.
The MYH9 gene, encodes the nonmuscle myosin heavy chain IIA, expressed in different tissues and especially in podocytes and mesangial cells. The disorder is characterized by the presence of macrothrombocytopenia, leukocyte inclusions and a variable risk of developing renal …
The MYH9 gene, encodes the nonmuscle myosin heavy chain IIA, expressed in different tissues and especially in podocytes and mesangial cells. …
Barakat syndrome revisited.
Barakat AJ, Raygada M, Rennert OM. Barakat AJ, et al. Am J Med Genet A. 2018 Jun;176(6):1341-1348. doi: 10.1002/ajmg.a.38693. Epub 2018 Apr 16. Am J Med Genet A. 2018. PMID: 29663634 Review.
Barakat syndrome also known as HDR syndrome (Online Mendelian Inheritance in Man [OMIM] 146255), was first described by Barakat et al. in . It is a rare genetic disorder characterized by the triad of hypoparathyroidism "H," sensorineural deafness "D," and renal dise …
Barakat syndrome also known as HDR syndrome (Online Mendelian Inheritance in Man [OMIM] 146255), was first described by Barakat et al. in . …
Surgical Management of Intractable Meniere's Disease.
Luca P, Ralli M, Cassandro C, Russo FY, Gioacchini FM, Cavaliere M, Fiore M, Greco A, Cassandro E, Scarpa A. Luca P, et al. Int Tinnitus J. 2022 Jun 21;26(1):50-56. doi: 10.5935/0946-5448.20220007. Int Tinnitus J. 2022. PMID: 35861458 Review.
Meniere's Disease (MD) is an inner ear disorder characterized by spontaneous recurrent vertigo, fluctuating sensorineural hearing loss, aural fullness and low-pitch tinnitus. ...A minority of cases is characterized by frequent vertigo attacks, progress …
Meniere's Disease (MD) is an inner ear disorder characterized by spontaneous recurrent vertigo, fluctuating sensorineural h …
Association between vitiligo and hearing loss.
Ma SH, Ang MD, Chang YT, Dai YX. Ma SH, et al. J Am Acad Dermatol. 2021 Dec;85(6):1465-1472. doi: 10.1016/j.jaad.2020.12.029. Epub 2021 Jan 22. J Am Acad Dermatol. 2021. PMID: 33359081
However, the relationship between vitiligo and sensorineural hearing loss (SNHL) remains uncertain. OBJECTIVE: We investigated the association between vitiligo and SNHL. ...These results suggest audiologic assessment for early recognition and management of …
However, the relationship between vitiligo and sensorineural hearing loss (SNHL) remains uncertain. OBJECTIVE: We inves …
Pendred syndrome.
Wémeau JL, Kopp P. Wémeau JL, et al. Best Pract Res Clin Endocrinol Metab. 2017 Mar;31(2):213-224. doi: 10.1016/j.beem.2017.04.011. Epub 2017 May 10. Best Pract Res Clin Endocrinol Metab. 2017. PMID: 28648509 Review.
Pendred syndrome is an autosomal recessive disorder that is classically defined by the combination of sensorineural deafness/hearing impairment, goiter, and an abnormal organification of iodide with or without hypothyroidism. The hallmark of the syndrome is t …
Pendred syndrome is an autosomal recessive disorder that is classically defined by the combination of sensorineural deafness/ …
Morphine-induced hearing loss.
Leache L, Aquerreta I, Moraza L, Ortega A. Leache L, et al. Am J Health Syst Pharm. 2016 Nov 15;73(22):1840-1843. doi: 10.2146/ajhp151012. Am J Health Syst Pharm. 2016. PMID: 27821396
PURPOSE: A case of severe bilateral sensorineural hearing loss associated with oral morphine is reported. ...Brain magnetic resonance imaging discarded other possible causes of hearing loss. Our patient's hearing loss did not resol …
PURPOSE: A case of severe bilateral sensorineural hearing loss associated with oral morphine is reported. ...Brain magn …
11,989 results
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