2-propanol has been researched along with Hearing Loss, Sensorineural in 7 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.
Hearing Loss, Sensorineural: Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Clinically, coloboma has been described as a feature in a WDR37-related disorder and a PACS1-related disorder (Schuurs-Hoeijmakers syndrome), but not in a PACS2-related disorder." | 2.72 | Coloboma may be a shared feature in a spectrum of disorders caused by mutations in the WDR37-PACS1-PACS2 axis. ( Kosaki, K; Miyama, S; Sakaguchi, Y; Takenouchi, T; Uehara, T; Yoshihashi, H, 2021) |
| "A girl with coloboma of the iris, sensorineural deafness, growth delay, distinctive face, and cranial nerve dysfunction was diagnosed of CHARGE association in the first year of life." | 1.32 | Hyper-IgM syndrome with CHARGE association. ( Aragón, P; Bahillo, P; Cambronero, R; Cantero, T; Gómez, S; Solís, P, 2003) |
| "Rieger syndrome is a dysembryogenetic disease in which labyrinthic damage can be associated with other genetic anomalies." | 1.32 | Rieger syndrome: case report. ( Megighian, D; Poli, P; Savastano, M, 2003) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 4 (57.14) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Sakaguchi, Y | 1 |
| Yoshihashi, H | 1 |
| Uehara, T | 1 |
| Miyama, S | 1 |
| Kosaki, K | 1 |
| Takenouchi, T | 1 |
| Gironi, LC | 1 |
| Zottarelli, F | 1 |
| Savoldi, G | 1 |
| Notarangelo, LD | 1 |
| Basso, ME | 1 |
| Ferrero, I | 1 |
| Timeus, F | 1 |
| Fagioli, F | 1 |
| Maiuri, L | 1 |
| Colombo, E | 1 |
| Savoia, P | 1 |
| Vieira, H | 1 |
| Gregory-Evans, K | 1 |
| Lim, N | 1 |
| Brookes, JL | 1 |
| Brueton, LA | 1 |
| Gregory-Evans, CY | 1 |
| Bahillo, P | 1 |
| Cantero, T | 1 |
| Solís, P | 1 |
| Aragón, P | 1 |
| Gómez, S | 1 |
| Cambronero, R | 1 |
| Megighian, D | 1 |
| Savastano, M | 1 |
| Poli, P | 1 |
| Avunduk, AM | 1 |
| Aslan, Y | 1 |
| Kapicioğlu, Z | 1 |
| Elmas, R | 1 |
| Stratton, RF | 1 |
| Bluestone, DL | 1 |
2 reviews available for 2-propanol and Hearing Loss, Sensorineural
| Article | Year |
|---|---|
Coloboma may be a shared feature in a spectrum of disorders caused by mutations in the WDR37-PACS1-PACS2 axis.
Topics: Abnormalities, Multiple; Amino Acid Substitution; Cerebellum; Choroid; Coloboma; Craniofacial Abnorm | 2021 |
Oto-palatal-digital syndrome type II with X-linked cerebellar hypoplasia/hydrocephalus.
Topics: Abnormalities, Multiple; Cerebellum; Cleft Palate; Coloboma; Hearing Loss; Hearing Loss, Bilateral; | 1991 |
5 other studies available for 2-propanol and Hearing Loss, Sensorineural
| Article | Year |
|---|---|
Congenital Hypopigmentary Disorders with Multiorgan Impairment: A Case Report and an Overview on Gray Hair Syndromes.
Topics: Abnormalities, Multiple; Adult; Chediak-Higashi Syndrome; Child, Preschool; Craniofacial Abnormaliti | 2019 |
First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
Topics: Adult; Child, Preschool; Chromosome Mapping; Chromosomes, Human, Pair 20; Coloboma; DNA Mutational A | 2002 |
Hyper-IgM syndrome with CHARGE association.
Topics: Abnormalities, Multiple; Child, Preschool; Choanal Atresia; Coloboma; Cranial Nerve Diseases; Face; | 2003 |
Rieger syndrome: case report.
Topics: Adult; Atrophy; Audiometry, Pure-Tone; Auditory Threshold; Brain Stem; Ear, Inner; Eye Abnormalities | 2003 |
High myopia, hypertelorism, iris coloboma, exomphalos, absent corpus callosum, and sensorineural deafness: report of a case and further evidence for autosomal recessive inheritance.
Topics: Abnormalities, Multiple; Agenesis of Corpus Callosum; Coloboma; Consanguinity; Corpus Callosum; Exop | 2000 |