2-propanol has been researched along with Hirschsprung Disease in 8 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.
Hirschsprung Disease: Congenital MEGACOLON resulting from the absence of ganglion cells (aganglionosis) in a distal segment of the LARGE INTESTINE. The aganglionic segment is permanently contracted thus causing dilatation proximal to it. In most cases, the aganglionic segment is within the RECTUM and SIGMOID COLON.
Excerpt | Relevance | Reference |
---|---|---|
"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) |
"Association of imperforate anus and Hirschsprung's disease is rare, the incidence of both events occurring together would be one child out of every 25 million live births." | 1.27 | Association of Hirschsprung's disease and imperforate anus in a patient with "cat-eye" syndrome. A report of one case and review of the literature. ( Mahboubi, S; Templeton, JM, 1984) |
"Two of the children, one with a coloboma and one without, are from the same consanguineous pedigree." | 1.27 | Unknown syndrome: Hirschsprung's disease, microcephaly, and iris coloboma: a new syndrome of defective neuronal migration. ( Brett, EM; Hurst, JA; Kumar, D; Markiewicz, M, 1988) |
"The child has mild developmental delay, coloboma of the right eye, and Hirschsprung's disease." | 1.27 | Concurrent de novo interstitial deletion of band 2p22 and reciprocal translocation (3;7)(p21;q22). ( Campbell, NT; Keith, CG; Webb, GC, 1988) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (50.00) | 18.7374 |
1990's | 2 (25.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (12.50) | 24.3611 |
2020's | 1 (12.50) | 2.80 |
Authors | Studies |
---|---|
Zhang, L | 1 |
Wan, Y | 1 |
Wang, N | 1 |
Pattebahadur, R | 1 |
Singhi, S | 1 |
Maharana, PK | 1 |
Mahboubi, S | 1 |
Templeton, JM | 1 |
Ohnuma, K | 1 |
Imaizumi, K | 1 |
Masuno, M | 1 |
Nakamura, M | 1 |
Kuroki, Y | 1 |
Guion-Almeida, ML | 1 |
Richieri-Costa, A | 1 |
Hurst, JA | 1 |
Markiewicz, M | 1 |
Kumar, D | 1 |
Brett, EM | 1 |
Kaplan, P | 1 |
de Chaderévian, JP | 1 |
Webb, GC | 1 |
Keith, CG | 1 |
Campbell, NT | 1 |
8 other studies available for 2-propanol and Hirschsprung Disease
Article | Year |
---|---|
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-Shah Syndrome: a rare case in an Indian child.
Topics: Child; Correction of Hearing Impairment; Hirschsprung Disease; Humans; India; Iris; Male; Pigmentati | 2016 |
Association of Hirschsprung's disease and imperforate anus in a patient with "cat-eye" syndrome. A report of one case and review of the literature.
Topics: Anus, Imperforate; Coloboma; Heart Septal Defects, Ventricular; Hirschsprung Disease; Humans; Infant | 1984 |
Magnetic resonance imaging abnormalities of the brain in Goldberg-Shprintzen syndrome (Hirschsprung disease, microcephaly, and iris coloboma)
Topics: Brain; Coloboma; Hirschsprung Disease; Humans; Infant; Iris; Magnetic Resonance Imaging; Male; Micro | 1997 |
Callosal agenesis, iris coloboma, and megacolon in a Brazilian boy with Rubinstein-Taybi syndrome.
Topics: Agenesis of Corpus Callosum; Child; Coloboma; Corpus Callosum; Hirschsprung Disease; Humans; Iris; M | 1992 |
Unknown syndrome: Hirschsprung's disease, microcephaly, and iris coloboma: a new syndrome of defective neuronal migration.
Topics: Coloboma; Consanguinity; Female; Hirschsprung Disease; Humans; Infant, Newborn; Iris; Male; Microcep | 1988 |
Piebaldism-Waardenburg syndrome: histopathologic evidence for a neural crest syndrome.
Topics: Abnormalities, Multiple; Eye Color; Hirschsprung Disease; Humans; Infant; Iris; Male; Neural Crest; | 1988 |
Concurrent de novo interstitial deletion of band 2p22 and reciprocal translocation (3;7)(p21;q22).
Topics: Abnormalities, Multiple; Adult; Child, Preschool; Chromosome Banding; Chromosome Deletion; Chromosom | 1988 |