Page last updated: 2024-10-29

2-propanol and Genetic Diseases, X-Chromosome Linked

2-propanol has been researched along with Genetic Diseases, X-Chromosome Linked in 10 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 Excerpts

ExcerptRelevanceReference
"The retinal detachment was managed with translimbal iridectomy, lensectomy, capsulectomy, and vitrectomy."1.46Repair of Total Tractional Retinal Detachment in Norrie Disease: Report of Technique and Successful Surgical Outcome. ( Capone, A; Thanos, A; Todorich, B; Yonekawa, Y, 2017)

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19902 (20.00)18.7374
1990's0 (0.00)18.2507
2000's2 (20.00)29.6817
2010's5 (50.00)24.3611
2020's1 (10.00)2.80

Authors

AuthorsStudies
Jacobson, A1
Bohnsack, BL1
Chang, TC1
Bauer, M1
Puerta, HS1
Greenberg, MB1
Cavuoto, KM1
Galvis, V1
Tello, A1
Rangel, CM1
Carreño, NI1
Berrospi, RD1
Niño, CA1
Morlino, S1
Alesi, V1
Calì, F1
Lepri, FR1
Secinaro, A1
Grammatico, P1
Novelli, A1
Drago, F1
Castori, M1
Baban, A1
Todorich, B1
Thanos, A1
Yonekawa, Y1
Capone, A1
Fang, S1
Guo, X1
Jia, X1
Xiao, X1
Li, S1
Zhang, Q1
Hu, J1
Liang, D1
Xue, J1
Liu, J1
Wu, L1
WEEKERS, R1
WATILLON, M1
DEITCH, RD1
WILSON, FM1
Reisli, I1
Artac, H1
van der Burg, M1
Ozturk, BT1

Other Studies

10 other studies available for 2-propanol and Genetic Diseases, X-Chromosome Linked

ArticleYear
Anterior megalophthalmos in sisters with Witteveen-Kolk syndrome.
    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus, 2022, Volume: 26, Issue:3

    Topics: Eye Abnormalities; Eye Diseases, Hereditary; Female; Genetic Diseases, X-Linked; Humans; Hydrophthal

2022
Ophthalmic findings in Frank-ter Haar syndrome: report of a sibling pair.
    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus, 2017, Volume: 21, Issue:6

    Topics: Abnormalities, Multiple; Adaptor Proteins, Signal Transducing; Amblyopia; Child, Preschool; Choroid;

2017
Iris-clip versus iris-claw intraocular lenses.
    Journal of cataract and refractive surgery, 2018, Volume: 44, Issue:11

    Topics: Cataract; Eye Diseases, Hereditary; Follow-Up Studies; Genetic Diseases, X-Linked; Humans; Iris; Len

2018
LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant.
    American journal of medical genetics. Part A, 2019, Volume: 179, Issue:1

    Topics: Adolescent; Child; Corneal Diseases; Ectopia Lentis; Eye Diseases, Hereditary; Female; Genetic Disea

2019
Repair of Total Tractional Retinal Detachment in Norrie Disease: Report of Technique and Successful Surgical Outcome.
    Ophthalmic surgery, lasers & imaging retina, 2017, 03-01, Volume: 48, Issue:3

    Topics: Blindness; Fluorescein Angiography; Follow-Up Studies; Fundus Oculi; Genetic Diseases, X-Linked; Hum

2017
Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism.
    Molecular vision, 2008, Volume: 14

    Topics: Adolescent; Adult; Albinism, Ocular; Asian People; Base Sequence; Child; Child, Preschool; China; DN

2008
A novel GPR143 splicing mutation in a Chinese family with X-linked congenital nystagmus.
    Molecular vision, 2011, Mar-12, Volume: 17

    Topics: Adolescent; Adult; Asian People; Base Sequence; Child; China; DNA Mutational Analysis; Eye Proteins;

2011
[Congenital glaucoma without megalocornea; clinical studies].
    Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde, 1957, Volume: 133, Issue:1

    Topics: Child; Eye Diseases, Hereditary; Genetic Diseases, X-Linked; Glaucoma; Humans; Infant; Iris

1957
Leukemic reticuloendotheliosis with presenting ocular complaints. Report of a case.
    Archives of ophthalmology (Chicago, Ill. : 1960), 1963, Volume: 69

    Topics: Eye; Eye Manifestations; Eye Neoplasms; Genetic Diseases, X-Linked; Humans; Iris; Leukemia; Leukemia

1963
Iris atrophy in a patient with X-linked agammaglobulinemia.
    Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, 2007, Volume: 42, Issue:6

    Topics: Agammaglobulinaemia Tyrosine Kinase; Agammaglobulinemia; Atrophy; Child, Preschool; Consanguinity; D

2007