2-propanol has been researched along with Klein Syndrome 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "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) |
| "We present a toddler with Waardenburg syndrome type 1 who was referred to our service for developmental delay concerns." | 1.91 | Association of autism spectrum disorder with Waardenburg syndrome in a toddler. ( George, FSA; Sam, LE; Tanwar, M; Wall, L, 2023) |
| "There are four types of Waardenburg syndrome (1-4) with different characteristics." | 1.72 | Waardenburg syndrome type 4 coexisting with open-angle glaucoma: a case report. ( Wan, Y; Wang, N; Zhang, L, 2022) |
| "The Waardenburg syndrome is a group of rare genetic diseases, which clinical manifestations include neurosensory hearing loss, diminished pigmentation of forelock in the frontal region, iris heterochromia, medial canthus dystopia, and the presence of such changes in first-line relatives." | 1.51 | [Ophthalmologic manifestations of Waardenburg syndrome]. ( Astakhov, SY; Astakhov, YS; Lisochkina, AB; Shakhnazarova, AA; Takhtaev, YV; Tultseva, SN, 2019) |
| "Waardenburg syndrome is a rare genetic disorder characterized by varying degree of deafness associated with pigmentary anomaly and defects of neural crest cell derived structures." | 1.39 | Waardenburg syndrome--a case report. ( Bansal, Y; Goyal, G; Jain, P; Mishra, C; Singh, M, 2013) |
| "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) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 21 (52.50) | 18.7374 |
| 1990's | 3 (7.50) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 11 (27.50) | 24.3611 |
| 2020's | 5 (12.50) | 2.80 |
| Authors | Studies |
|---|---|
| Park, JG | 1 |
| Randhawa, S | 1 |
| Capone, A | 1 |
| Zhang, L | 1 |
| Wan, Y | 1 |
| Wang, N | 1 |
| Woldetensaye, AG | 1 |
| Runyan, CM | 1 |
| Koerner, JC | 1 |
| George, FSA | 1 |
| Sam, LE | 1 |
| Tanwar, M | 1 |
| Wall, L | 1 |
| Kumawat, D | 1 |
| Kumar, V | 1 |
| Sahay, P | 1 |
| Nongrem, G | 1 |
| Chandra, P | 1 |
| Astakhov, YS | 1 |
| Tultseva, SN | 1 |
| Lisochkina, AB | 1 |
| Takhtaev, YV | 1 |
| Astakhov, SY | 1 |
| Shakhnazarova, AA | 1 |
| Zhang, W | 1 |
| Xiao, L | 1 |
| Chen, B | 1 |
| Xu, Y | 1 |
| Yan, N | 1 |
| Dave, TV | 1 |
| Pappuru, RR | 1 |
| Dave, VP | 1 |
| Nasser, LS | 1 |
| Paranaíba, LM | 1 |
| Frota, AC | 1 |
| Gomes, A | 1 |
| Versiani, G | 1 |
| Martelli Júnior, H | 1 |
| Akal, A | 1 |
| Göncü, T | 1 |
| Boyaci, N | 1 |
| Yılmaz, ÖF | 1 |
| Okamura, K | 1 |
| Oiso, N | 1 |
| Tamiya, G | 1 |
| Makino, S | 1 |
| Tsujioka, D | 1 |
| Abe, Y | 1 |
| Kawaguchi, M | 1 |
| Hozumi, Y | 1 |
| Shimomura, Y | 1 |
| Suzuki, T | 1 |
| Chen, Y | 1 |
| Yang, F | 1 |
| Zheng, H | 1 |
| Zhou, J | 1 |
| Zhu, G | 1 |
| Hu, P | 1 |
| Wu, W | 1 |
| Pattebahadur, R | 1 |
| Singhi, S | 1 |
| Maharana, PK | 1 |
| Issa, S | 1 |
| Bondurand, N | 1 |
| Faubert, E | 1 |
| Poisson, S | 1 |
| Lecerf, L | 1 |
| Nitschke, P | 1 |
| Deggouj, N | 1 |
| Loundon, N | 1 |
| Jonard, L | 1 |
| David, A | 1 |
| Sznajer, Y | 1 |
| Blanchet, P | 1 |
| Marlin, S | 1 |
| Pingault, V | 1 |
| Rennie, IG | 1 |
| Bansal, Y | 1 |
| Jain, P | 1 |
| Goyal, G | 1 |
| Singh, M | 1 |
| Mishra, C | 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 |
| RUGEL, SJ | 1 |
| KEATES, EU | 1 |
| PAUFIQUE, L | 1 |
| RAVAULT, MP | 1 |
| MORGON, A | 1 |
| BEAVER, R | 1 |
| ROBINSON, GC | 1 |
| MILLER, JR | 1 |
| SOEPARDEN, LI | 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 |
| Shah, KN | 1 |
| Dalal, SJ | 1 |
| Desai, MP | 1 |
| Sheth, PN | 1 |
| Joshi, NC | 1 |
| Ambani, LM | 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 |
| Mullaney, PB | 1 |
| Parsons, MA | 1 |
| Weatherhead, RG | 1 |
| Karcioglu, ZA | 1 |
| Bard, LA | 1 |
| Jones, KL | 1 |
| Smith, DW | 1 |
| Harvey, MA | 1 |
| Hall, BD | 1 |
| Quan, L | 1 |
| Hayasaka, S | 1 |
| Noda, S | 1 |
| Setogawa, T | 1 |
| Kobayashi, A | 1 |
| Kishida, K | 1 |
| Sakai, T | 1 |
| Kaplan, P | 1 |
| de Chaderévian, JP | 1 |
| Mohamed, MA | 1 |
| Schulze, W | 1 |
| Ganz, H | 1 |
| Biéder, J | 1 |
| Faidherbe, D | 1 |
| Houillon, P | 1 |
| Amini-Elihou, S | 1 |
| Ahrendts, H | 1 |
3 reviews available for 2-propanol and Klein Syndrome
| Article | Year |
|---|---|
Don't it make my blue eyes brown: heterochromia and other abnormalities of the iris.
Topics: Adenocarcinoma; Adenoma; Female; Horner Syndrome; Humans; Immunohistochemistry; Iris; Iris Diseases; | 2012 |
[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 |
37 other studies available for 2-propanol and Klein Syndrome
| Article | Year |
|---|---|
Iris Heterochromia and Choroidal Hypopigmentation in Waardenburg Syndrome.
Topics: Humans; Hypopigmentation; Iris; Iris Diseases; Waardenburg Syndrome | 2023 |
Waardenburg syndrome type 4 coexisting with open-angle glaucoma: a case report.
Topics: Adult; Amino Acids; Glaucoma, Open-Angle; Hirschsprung Disease; Humans; Hypopigmentation; Iris; Male | 2022 |
Waardenburg syndrome-associated neurotrophic keratopathy in a child treated with neurotization surgery.
Topics: Child; Corneal Dystrophies, Hereditary; Humans; Hypopigmentation; Iris; Iris Diseases; Nerve Transfe | 2022 |
Association of autism spectrum disorder with Waardenburg syndrome in a toddler.
Topics: Autism Spectrum Disorder; Child, Preschool; Hair; Humans; Infant, Newborn; Iris; Rare Diseases; Skin | 2023 |
Bilateral asymmetrical partial heterochromia of iris and fundus in Waardenburg syndrome type 2A with a novel
Topics: Child, Preschool; DNA; Female; Humans; Iris; Iris Diseases; Microphthalmia-Associated Transcription | 2019 |
[Ophthalmologic manifestations of Waardenburg syndrome].
Topics: Fluorescein Angiography; Humans; Iris; Iris Diseases; Pigmentation Disorders; Waardenburg Syndrome | 2019 |
22q12.3-q13.1 microdeletion including
Topics: Chromosomes, Human, Pair 22; Exome Sequencing; Humans; Infant; Iris; Male; Mutation; Pedigree; SOXE | 2021 |
When color matters: Waardenburg syndrome.
Topics: Adult; Choroid; Diagnosis, Differential; Female; Genetic Testing; Humans; Iris; Waardenburg Syndrome | 2019 |
[Waardenburg syndrome--ophthalmic findings and criteria for diagnosis: case reports].
Topics: Adult; Child, Preschool; Eye Diseases, Hereditary; Female; Genetic Predisposition to Disease; Humans | 2012 |
Anisometropic amblyopia in a case of type 2 Waardenburg syndrome.
Topics: Amblyopia; Child; Humans; Iris; Iris Diseases; Male; Pigmentation Disorders; Visual Acuity; Waardenb | 2013 |
Waardenburg syndrome type IIE in a Japanese patient caused by a novel missense mutation in the SOX10 gene.
Topics: Asian People; Humans; Iris; Japan; Male; Mutation, Missense; SOXE Transcription Factors; Waardenburg | 2015 |
Clinical and genetic investigation of families with type II Waardenburg syndrome.
Topics: Asian People; Base Sequence; China; DNA Mutational Analysis; Exons; Family; Female; Finger Joint; Ge | 2016 |
Waardenburg-Shah Syndrome: a rare case in an Indian child.
Topics: Child; Correction of Hearing Impairment; Hirschsprung Disease; Humans; India; Iris; Male; Pigmentati | 2016 |
EDNRB mutations cause Waardenburg syndrome type II in the heterozygous state.
Topics: Adolescent; Adult; Amino Acid Substitution; Child; Child, Preschool; Computational Biology; DNA Muta | 2017 |
Waardenburg syndrome--a case report.
Topics: Child; Cornea; Diagnosis, Differential; Female; Fundus Oculi; Genetic Predisposition to Disease; Hum | 2013 |
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 |
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 |
DEFECTIVE HEARING IN CHILDREN ATTENDING ORDINARY SCHOOLS.
Topics: Abnormalities, Drug-Induced; Child; Cleft Palate; Congenital Abnormalities; Female; Goiter; Hearing | 1965 |
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 |
[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 |
White forelock, pigmentary disorder of irides, and long segment Hirschsprung disease: possible variant of Waardenburg syndrome.
Topics: Abnormalities, Multiple; Female; Humans; Infant; Infant, Newborn; Intestinal Obstruction; Iris; Male | 1981 |
Clinical and morphological features of Waardenburg syndrome type II.
Topics: Cataract; Eye Color; Female; Humans; Infant; Iris; Iris Diseases; Microscopy, Electron; Pigmentation | 1998 |
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 |
Older paternal age and fresh gene mutation: data on additional disorders.
Topics: Age Factors; Bone Cysts; Brain Diseases; Carcinoma, Basal Cell; Cleidocranial Dysplasia; Congenital | 1975 |
Piebaldism-Waardenburg syndrome: histopathologic evidence for a neural crest syndrome.
Topics: Abnormalities, Multiple; Eye Color; Hirschsprung Disease; Humans; Infant; Iris; Male; Neural Crest; | 1988 |
Inter-oculo-irido-auditory dysplasia. (Waardenburg, van der Hoeve, Halberstsma syndrome).
Topics: Abnormalities, Multiple; Child; Deafness; Egypt; Eye Abnormalities; Female; Humans; Iris; Osteogenes | 1971 |
[Hearing disorders in Waardenburg's syndrome].
Topics: Abnormalities, Multiple; Adult; Audiometry; Child; Child, Preschool; Deafness; Eyebrows; Humans; Iri | 1972 |
[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 |
[Waardenburg's syndrome demonstrated on 5 families].
Topics: Adolescent; Adult; Child; Deafness; Female; Fundus Oculi; Humans; Iris; Male; Malocclusion; Nose Def | 1965 |