Page last updated: 2024-10-29

2-propanol and Deafness, Transitory

2-propanol has been researched along with Deafness, Transitory in 12 studies

2-Propanol: An isomer of 1-PROPANOL. It is a colorless liquid having disinfectant properties. It is used in the manufacture of acetone and its derivatives and as a solvent. Topically, it is used as an antiseptic.
propan-2-ol : A secondary alcohol that is propane in which one of the hydrogens attached to the central carbon is substituted by a hydroxy group.

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-19906 (50.00)18.7374
1990's1 (8.33)18.2507
2000's3 (25.00)29.6817
2010's2 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Silverstein, H1
Wycherly, BJ1
Alameda, Y1
Van Ess, MJ1
Sobreira, N1
Walsh, MF1
Batista, D1
Wang, T1
Shazly, TA1
Farrag, AN1
Kamel, A1
Al-Hussaini, AK1
PARTSCH, CJ1
HOUGHTON, NI1
RUGEL, SJ1
KEATES, EU1
PAUFIQUE, L1
RAVAULT, MP1
MORGON, A1
ROBINSON, GC1
MILLER, JR1
SOEPARDEN, LI1
Khoury, T1
Gonzalez-Fernandez, F1
Munschauer, FE1
Ostrow, P1
Stefaniu, I1
Chiotoroiu, S1
Epure, C1
Frasia, M1
Stratton, RF1
Bluestone, DL1
Abruzzo, MA1
Erickson, RP1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Correlation Between Pupil Size and Ocular Signs in Pseudoexfoliation Syndrome (PEX): a Contralateral Eye Study.[NCT05113121]100 participants (Actual)Observational [Patient Registry]2021-08-25Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

1 review available for 2-propanol and Deafness, Transitory

ArticleYear
Oto-palatal-digital syndrome type II with X-linked cerebellar hypoplasia/hydrocephalus.
    American journal of medical genetics, 1991, Nov-01, Volume: 41, Issue:2

    Topics: Abnormalities, Multiple; Cerebellum; Cleft Palate; Coloboma; Hearing Loss; Hearing Loss, Bilateral;

1991

Trials

1 trial available for 2-propanol and Deafness, Transitory

ArticleYear
A prospective study to evaluate the efficacy of isopropyl alcohol irrigations to prevent cerumen impaction.
    Ear, nose, & throat journal, 2012, Volume: 91, Issue:3

    Topics: 2-Propanol; Aged; Aged, 80 and over; Cerumen; Ear Canal; Female; Hearing Loss; Humans; Male; Middle

2012

Other Studies

10 other studies available for 2-propanol and Deafness, Transitory

ArticleYear
Interstitial deletion 5q14.3-q21 associated with iris coloboma, hearing loss, dental anomaly, moderate intellectual disability, and attention deficit and hyperactivity disorder.
    American journal of medical genetics. Part A, 2009, Volume: 149A, Issue:11

    Topics: Attention Deficit Disorder with Hyperactivity; Child; Chromosome Deletion; Chromosomes, Human, Pair

2009
Prevalence of pseudoexfoliation syndrome and pseudoexfoliation glaucoma in Upper Egypt.
    BMC ophthalmology, 2011, Jun-27, Volume: 11

    Topics: Adult; Age Distribution; Aged; Aged, 80 and over; Cataract; Corneal Opacity; Egypt; Exfoliation Synd

2011
[Hereditary deafness in the Waardenburg-Klein syndrome].
    Zeitschrift fur Laryngologie, Rhinologie, Otologie und ihre Grenzgebiete, 1962, Volume: 41

    Topics: Albinism; Bone Diseases; Deafness; Genetics, Medical; Hearing Loss; Humans; Iris; Nose; Nose Deformi

1962
WAARDENBURG'S SYNDROME WITH DEAFNESS AS THE PRESENTING SYMPTOM. REPORT OF TWO CASES.
    The New Zealand medical journal, 1964, Volume: 63

    Topics: Child; Congenital Abnormalities; Deafness; Eyebrows; Eyelids; Genetics, Medical; Hair; Hearing Loss;

1964
WAARDENBURG'S SYNDROME IN SIX GENERATIONS OF ONE FAMILY.
    American journal of diseases of children (1960), 1965, Volume: 109

    Topics: Congenital Abnormalities; Deafness; Eyelids; Facial Expression; Genetics, Medical; Hair; Hearing Los

1965
[APROPOS OF THE WAARDENBURG-KLEIN SYNDROME].
    Bulletin des societes d'ophtalmologie de France, 1964, Volume: 64

    Topics: Child; Deafness; Eye Diseases; Hearing Loss; Humans; Iris; Lacrimal Apparatus; Nose; Nose Deformitie

1964
WAARDENBURG'S SYNDROME: THE RISK OF RECURRENCE OF CONGENITAL DEAFNESS IN A KINDRED.
    The Journal of pediatrics, 1965, Volume: 67

    Topics: Congenital Abnormalities; Deafness; Eyebrows; Eyelids; Genetics, Medical; Hair; Hearing Loss; Humans

1965
A 47-year-old man with sudden onset of blindness, pleocytosis, and temporary hearing loss. Vogt-Koyanagi-Harada syndrome (Uveomeningoencephalitic syndrome).
    Archives of pathology & laboratory medicine, 2006, Volume: 130, Issue:7

    Topics: Blindness; Choroid; Fatal Outcome; Hearing Loss; Humans; Iris; Leukocytosis; Male; Middle Aged; Uveo

2006
[Irido-corneal dysgenesis, Axenfeld Rieger syndrome].
    Oftalmologia (Bucharest, Romania : 1990), 2007, Volume: 51, Issue:2

    Topics: Abnormalities, Multiple; Adult; Anterior Eye Segment; Corneal Opacity; Diagnosis, Differential; Eye

2007
Re-evaluation of new X-linked syndrome for evidence of CHARGE syndrome or association.
    American journal of medical genetics, 1989, Volume: 34, Issue:3

    Topics: Abnormalities, Multiple; Adolescent; Cleft Palate; Coloboma; Dwarfism; Ear; Follow-Up Studies; Heari

1989