2-propanol has been researched along with Deafness in 40 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.
Deafness: A general term for the complete loss of the ability to hear from both ears.
Excerpt | Relevance | Reference |
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"Waardenburg's syndrome consists of lateral displacement of the inner canthi of the eyes (dystopia canthorum), a broad nasal root and confluent eyebrows, heterochromia iridum, a white forelock and congenital deafness." | 3.64 | WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION. ( PARTINGTON, MW, 1964) |
"Waardenburg-Klein syndrome is an "Oculo-dermato-auditif" dysplasia described in 1947 by Waardenburg and by Klein in 1950." | 2.40 | [A case of Waardenburg-Klein syndrome observed at the Cotonou NUHC]. ( Babagbeto, M; Bassabi, SK; Doutetien, C; Hounkpe, YY; Latoundji, S; Medji, AP; Oussa, G; Vodouhe, SJ, 1997) |
"One child had an iris coloboma." | 1.29 | Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder? ( Barrow, M; Donnai, D, 1993) |
"Eighty-nine children with the Waardenburg syndrome were identified during diagnostic surveys of 3006 deaf children attending 19 special schools in southern Africa." | 1.27 | The Waardenburg syndrome in deaf children in southern Africa. ( Beighton, P; Sellars, S, 1983) |
"In addition to acronymic features of Coloboma, Heart disease, Atresia of the choanae, Retarded growth and development, Genital hypoplasia, and Ear anomalies, other important diagnostic features include facial paralysis and feeding problems suggestive of velopharyngeal incompetency." | 1.27 | The spectrum of clinical features in CHARGE syndrome. ( Davenport, SL; Hefner, MA; Mitchell, JA, 1986) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 35 (87.50) | 18.7374 |
1990's | 4 (10.00) | 18.2507 |
2000's | 1 (2.50) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
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Magdesian, KG | 1 |
Williams, DC | 1 |
Aleman, M | 1 |
Lecouteur, RA | 1 |
Madigan, JE | 1 |
BROBECK, VH | 1 |
FLEISCHLI, CA | 1 |
DIGEORGE, AM | 1 |
OLMSTED, RW | 1 |
HARLEY, RD | 1 |
PARTSCH, CJ | 1 |
HOUGHTON, NI | 1 |
COUTEAU-LAGARDE, JM | 1 |
COLLIER, M | 1 |
PARTINGTON, MW | 1 |
NATH, K | 1 |
VIJAY, SD | 1 |
NEMA, HV | 1 |
SHUKLA, BR | 1 |
RUGEL, SJ | 1 |
KEATES, EU | 1 |
PAUFIQUE, L | 1 |
RAVAULT, MP | 1 |
MORGON, A | 1 |
ROBINSON, GC | 3 |
MILLER, JR | 1 |
SOEPARDEN, LI | 1 |
POROT, M | 2 |
FILIU, M | 1 |
Uyama, S | 1 |
Aikawa, K | 1 |
Tomemori, S | 1 |
Feingold, M | 1 |
Robinson, MJ | 1 |
Gellis, SS | 1 |
Sellars, S | 1 |
Beighton, P | 1 |
Donnai, D | 1 |
Barrow, M | 1 |
Bassabi, SK | 1 |
Medji, AP | 1 |
Doutetien, C | 1 |
Oussa, G | 1 |
Hounkpe, YY | 1 |
Vodouhe, SJ | 1 |
Babagbeto, M | 1 |
Latoundji, S | 1 |
Bard, LA | 1 |
Hayasaka, S | 1 |
Noda, S | 1 |
Setogawa, T | 1 |
Kobayashi, A | 1 |
Kishida, K | 1 |
Sakai, T | 1 |
Warburg, M | 1 |
Tommerup, N | 1 |
Vestermark, S | 1 |
Parving, A | 1 |
Weismann, K | 1 |
Russell, B | 1 |
Thomsen, HK | 1 |
Davenport, SL | 1 |
Hefner, MA | 1 |
Mitchell, JA | 1 |
de Chadarévian, JP | 1 |
Kaplan, P | 1 |
Vekemans, M | 1 |
Kaplan, BS | 1 |
Bradley, WG | 1 |
Richardson, J | 1 |
Frew, IJ | 1 |
Mair, IW | 1 |
Pollard, G | 1 |
Neumaier, R | 1 |
Remlein-Mozolewska, G | 1 |
Roberts, SR | 1 |
Mohamed, MA | 1 |
Weiss, DI | 1 |
Ziring, PR | 1 |
Cooper, LZ | 1 |
Schulze, W | 1 |
Ganz, H | 1 |
Oba, N | 1 |
Biéder, J | 1 |
Faidherbe, D | 1 |
Houillon, P | 1 |
Amini-Elihou, S | 1 |
Amin-Zaki, L | 1 |
Wright, VJ | 1 |
Gorlin, RJ | 1 |
Hertzberg, R | 1 |
Ahrendts, H | 1 |
2 reviews available for 2-propanol and Deafness
Article | Year |
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[A case of Waardenburg-Klein syndrome observed at the Cotonou NUHC].
Topics: Benin; Child, Preschool; Deafness; Humans; Iris; Male; Waardenburg Syndrome | 1997 |
Waardenburg syndrome in Japanese patients. Case reports and literature review.
Topics: Adult; Albinism, Ocular; Child, Preschool; Deafness; Eye Color; Female; Humans; Incidence; Infant; I | 1992 |
38 other studies available for 2-propanol and Deafness
Article | Year |
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Evaluation of deafness in American Paint Horses by phenotype, brainstem auditory-evoked responses, and endothelin receptor B genotype.
Topics: Animals; Behavior, Animal; Deafness; Evoked Potentials, Auditory, Brain Stem; Female; Genetic Predis | 2009 |
Cataract, recurrent iritis, and deafness secondary to injury by lightning.
Topics: Cataract; Deafness; Electric Injuries; Electricity; Humans; Inflammation; Iris; Iritis; Lightning | 1946 |
Waardenburg's syndrome. A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects.
Topics: Deafness; Eye Abnormalities; Eyelids; Humans; Iris; Lacrimal Apparatus; Waardenburg Syndrome | 1960 |
[Hereditary deafness in the Waardenburg-Klein syndrome].
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.
Topics: Child; Congenital Abnormalities; Deafness; Eyebrows; Eyelids; Genetics, Medical; Hair; Hearing Loss; | 1964 |
[THE WHITE FORELOCK AND MYOPIA AS "INDICATOR" FACTORS OF THE WAARDENBURG-KLEIN SYNDROME].
Topics: Child; Congenital Abnormalities; Deafness; Eyebrows; Eyelids; Genetics, Medical; Hair; Hair Diseases | 1963 |
WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION.
Topics: Adolescent; Anemia, Iron-Deficiency; Black People; Canada; Child; Deafness; Eye; Eyebrows; Eyelids; | 1964 |
CROUZON'S DISEASE AND PITUITARY DYSFUNCTION. CROUZON'S DISEASE, HYPOPITUITARISM, ECTOPIA LENTIS, SECONDARY GLAUCOMA, AND IRIS ATROPHY IN DEAF-MUTE FAMILY.
Topics: Adolescent; Atrophy; Craniofacial Dysostosis; Deafness; Ectopia Lentis; Eye Diseases; Genetics, Medi | 1964 |
WAARDENBURG'S SYNDROME IN SIX GENERATIONS OF ONE FAMILY.
Topics: Congenital Abnormalities; Deafness; Eyelids; Facial Expression; Genetics, Medical; Hair; Hearing Los | 1965 |
[APROPOS OF THE WAARDENBURG-KLEIN SYNDROME].
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.
Topics: Congenital Abnormalities; Deafness; Eyebrows; Eyelids; Genetics, Medical; Hair; Hearing Loss; Humans | 1965 |
[A curious syndrome: deaf-mutism, iridal heterochromia and epilepsy].
Topics: Deafness; Epilepsy; Eye Abnormalities; Humans; Iris; Iris Diseases; Medical Records; Syndrome; Trite | 1959 |
[A second case of deaf-mutism with heterochromia iridis and epilepsy].
Topics: Deafness; Epilepsy; Humans; Iris; Iris Diseases; Pigmentation Disorders | 1959 |
[Waardenburg's syndrome in three generations of one family].
Topics: Adult; Child, Preschool; Chromosomes; Deafness; Female; Humans; Iris; Male; Nose Deformities, Acquir | 1966 |
Waardenburg's syndrome during the first year of life.
Topics: Audiometry; Deafness; Fundus Oculi; Hair; Humans; Infant; Infant, Newborn; Iris; Male; Nose Deformit | 1967 |
The Waardenburg syndrome in deaf children in southern Africa.
Topics: Abnormalities, Multiple; Black or African American; Black People; Color; Deafness; Female; Humans; I | 1983 |
Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?
Topics: Abnormalities, Multiple; Agenesis of Corpus Callosum; Child, Preschool; Coloboma; Deafness; Female; | 1993 |
Heterogeneity in Waardenburg's syndrome. Report of a family with ocular albinism.
Topics: Abnormalities, Multiple; Adolescent; Adult; Albinism; Child; Child, Preschool; Deafness; Female; Gen | 1978 |
The Yemenite deaf-blind hypopigmentation syndrome. A new oculo-dermato-auditory syndrome.
Topics: Abnormalities, Multiple; Blindness; Child; Coloboma; Cytogenetics; Deafness; Female; Humans; Iris; M | 1990 |
The spectrum of clinical features in CHARGE syndrome.
Topics: Abnormalities, Multiple; Adolescent; Adult; Central Nervous System Diseases; Child, Preschool; Choan | 1986 |
Aniridia/glaucoma and Wilms tumor in a sibship with renal tubular acidosis and sensory nerve deafness.
Topics: Acidosis, Renal Tubular; Adult; Consanguinity; Deafness; Diabetes Mellitus, Type 1; Genes, Recessive | 1987 |
The familial association of neurofibromatosis, peroneal muscular atrophy, congenital deafness, partial albinism, and Axenfeld's defect.
Topics: Adult; Albinism; Congenital Abnormalities; Corneal Opacity; Deafness; Electromyography; Female; Fund | 1974 |
Hereditary deafness in the white cat.
Topics: Age Factors; Animals; Cats; Cochlea; Deafness; Ear, Inner; Female; Functional Laterality; Ganglia; G | 1973 |
Vision characteristics of deaf students.
Topics: Adolescent; Adult; Amblyopia; California; Cataract; Child; Child, Preschool; Color Vision Defects; D | 1974 |
[Case of iridoschisis in a 10-year-old girl].
Topics: Age Factors; Child; Deafness; Eye Diseases; Female; Humans; Iris | 1973 |
Color dilution and hereditary defects in collie dogs.
Topics: Animals; Blindness; Deafness; Dog Diseases; Dogs; Ear; Eye Abnormalities; Fundus Oculi; Genes; Hair; | 1967 |
Inter-oculo-irido-auditory dysplasia. (Waardenburg, van der Hoeve, Halberstsma syndrome).
Topics: Abnormalities, Multiple; Child; Deafness; Egypt; Eye Abnormalities; Female; Humans; Iris; Osteogenes | 1971 |
Surgery of the rubella cataract.
Topics: Abnormalities, Multiple; Age Factors; Cataract; Cataract Extraction; Child, Preschool; Deafness; Fem | 1972 |
[Hearing disorders in Waardenburg's syndrome].
Topics: Abnormalities, Multiple; Adult; Audiometry; Child; Child, Preschool; Deafness; Eyebrows; Humans; Iri | 1972 |
[A case report of a family of Rieger's anomaly].
Topics: Abnormalities, Multiple; Adult; Atropine; Child; Cornea; Deafness; Eye Diseases; Glaucoma; Humans; I | 1971 |
[Heterochromia iridis, hypoacousia and epilepsy in the same family].
Topics: Child; Child Behavior Disorders; Deafness; Epilepsy; Humans; Iris; Language Disorders; Male; Pigment | 1970 |
[A Swiss family with Klein-Waardenburg's syndrome associated with hyperkeratosis of the palms and feet and with serious oligophrenia].
Topics: Abnormalities, Multiple; Adolescent; Blood Cells; Child; Deafness; Diseases in Twins; Eye Diseases; | 1970 |
An Arab family with Waardenburg syndrome.
Topics: Abnormalities, Multiple; Adolescent; Adult; Deafness; Female; Humans; Iraq; Iris; Male; Middle Aged; | 1971 |
Sensorineural hearing loss and congenital heterochromia iridum. Report of a case.
Topics: Asian People; Audiometry; Child; Deafness; Ear, External; Humans; Iris; Male; Pigmentation Disorders | 1968 |
Sensorineural hearing loss and congenital heterochromia iridium.
Topics: Child; Color; Deafness; Ear; Humans; Iris | 1969 |
Sensorineural hearing loss and congenital heterochromia iridium.
Topics: Branchial Region; Child; Color; Deafness; Ear; Humans; Iris | 1969 |
Ocular defects in congenital rubella.
Topics: Atrophy; Cataract; Chorioretinitis; Deafness; Diagnosis, Differential; Edema; Eye Diseases; Female; | 1969 |
[Waardenburg's syndrome demonstrated on 5 families].
Topics: Adolescent; Adult; Child; Deafness; Female; Fundus Oculi; Humans; Iris; Male; Malocclusion; Nose Def | 1965 |