Page last updated: 2024-10-27

flumazenil and Cataract

flumazenil has been researched along with Cataract in 10 studies

Flumazenil: A potent benzodiazepine receptor antagonist. Since it reverses the sedative and other actions of benzodiazepines, it has been suggested as an antidote to benzodiazepine overdoses.
flumazenil : An organic heterotricyclic compound that is 5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine which is substituted at positions 3, 5, 6, and 8 by ethoxycarbonyl, methyl, oxo, and fluoro groups, respectively. It is used as an antidote to benzodiazepine overdose.

Cataract: Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, location) or etiology (cause and time of occurrence). (Dorland, 27th ed)

Research Excerpts

ExcerptRelevanceReference
"Management includes surgical treatment of the cataracts, and rehabilitation and corrective orthopaedic surgery for the peripheral neuropathy."2.43Congenital cataracts-facial dysmorphism-neuropathy. ( Kalaydjieva, L, 2006)
"The CCFDN syndrome is a complex phenotype involving multiple systems, characterized by facial dysmorphism, congenital cataracts, microcorneae, delayed early motor and intellectual development, hypogonadotrop hypogonadism, hypomyelination of the peripheral nervous system, and serious complications related to general anaesthesia."1.34[Congenital cataracts facial dysmorphism neuropathy syndrome--first Hungarian case report]. ( Molnár, MJ; Neuwirth, M; Rebecca, G; Siska, E, 2007)

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (10.00)18.2507
2000's7 (70.00)29.6817
2010's2 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Haret, D1
Lassuthova, P1
Sišková, D1
Haberlová, J1
Sakmaryová, I1
Filouš, A1
Seeman, P1
Herczegfalvi, A1
Pikó, H1
Karcagi, V1
Tzifi, F1
Pons, R1
Athanassaki, C1
Poulou, M1
Kanavakis, E1
Varon, R1
Gooding, R2
Steglich, C1
Marns, L1
Tang, H1
Angelicheva, D3
Yong, KK1
Ambrugger, P1
Reinhold, A1
Morar, B1
Baas, F1
Kwa, M1
Tournev, I1
Guerguelcheva, V1
Kremensky, I1
Lochmüller, H2
Müllner-Eidenböck, A1
Merlini, L2
Neumann, L1
Bürger, J1
Walter, M1
Swoboda, K1
Thomas, PK2
von Moers, A1
Risch, N1
Kalaydjieva, L4
Shabo, G1
Scheffer, H1
Cruysberg, JR1
Lammens, M1
Pasman, JW1
Spruit, M1
Willemsen, MA1
Siska, E1
Neuwirth, M1
Rebecca, G1
Molnár, MJ1
Turnev, I1
Dye, D1
Chandler, D1
Müller-Felber, W1
Walter, MC1
Talim, B1
Hallmayer, J1

Reviews

1 review available for flumazenil and Cataract

ArticleYear
Congenital cataracts-facial dysmorphism-neuropathy.
    Orphanet journal of rare diseases, 2006, Aug-29, Volume: 1

    Topics: Abnormalities, Multiple; Cataract; Chromosomes, Human, Pair 18; Face; Facial Nerve Diseases; Humans;

2006

Other Studies

9 other studies available for flumazenil and Cataract

ArticleYear
Rectal Flumazenil can save the day.
    Paediatric anaesthesia, 2008, Volume: 18, Issue:4

    Topics: Administration, Rectal; Anesthesia Recovery Period; Anti-Anxiety Agents; Antidotes; Cataract; Catara

2008
Congenital cataract, facial dysmorphism and demyelinating neuropathy (CCFDN) in 10 Czech Gypsy children--frequent and underestimated cause of disability among Czech Gypsies.
    Orphanet journal of rare diseases, 2014, Apr-01, Volume: 9

    Topics: Adolescent; Cataract; Child; Child, Preschool; Craniofacial Abnormalities; Czech Republic; Female; H

2014
[Screening for hereditary neuromuscular disorders with molecular genetic methods in the Roma population of Hungary].
    Ideggyogyaszati szemle, 2008, Nov-30, Volume: 61, Issue:11-12

    Topics: Cataract; Face; Founder Effect; Frameshift Mutation; Gene Deletion; Hereditary Sensory and Motor Neu

2008
Congenital cataracts, facial dysmorphism, and neuropathy syndrome.
    Pediatric neurology, 2011, Volume: 45, Issue:3

    Topics: Adult; Cataract; Face; Female; Humans; Infant, Newborn; Male; Mutation; Peripheral Nervous System Di

2011
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome.
    Nature genetics, 2003, Volume: 35, Issue:2

    Topics: Amino Acid Sequence; Base Sequence; Binding Sites; Cataract; Chromosome Mapping; Chromosomes, Human,

2003
Congenital cataract facial dysmorphism neuropathy syndrome: a clinically recognizable entity.
    Pediatric neurology, 2005, Volume: 33, Issue:4

    Topics: Cataract; Child, Preschool; Craniofacial Abnormalities; Diagnosis, Differential; Female; Humans; Neu

2005
[Congenital cataracts facial dysmorphism neuropathy syndrome--first Hungarian case report].
    Ideggyogyaszati szemle, 2007, May-30, Volume: 60, Issue:5-6

    Topics: Adolescent; Brain; Cataract; Child; Child, Preschool; Developmental Disabilities; Facial Nerve Disea

2007
Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qter.
    European journal of human genetics : EJHG, 1999, Volume: 7, Issue:5

    Topics: Adolescent; Adult; Cataract; Child; Child, Preschool; Chromosome Mapping; Chromosomes, Human, Pair 1

1999
Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromes.
    Neurology, 2002, Jan-22, Volume: 58, Issue:2

    Topics: Adolescent; Cataract; Child; Child, Preschool; Chromosomes, Human, Pair 18; Face; Female; Founder Ef

2002