2-propanol has been researched along with Growth Disorders in 19 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.
Growth Disorders: Deviations from the average values for a specific age and sex in any or all of the following: height, weight, skeletal proportions, osseous development, or maturation of features. Included here are both acceleration and retardation of growth.
| Excerpt | Relevance | Reference |
|---|---|---|
| "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) |
| "A 17-year-old female with Goltz's syndrome was examined because of visual acuity loss in her right eye." | 1.30 | Focal dermal hypoplasia (Goltz's syndrome). ( Erden, I; Günalp, I; Gündüz, K, 1997) |
| "Two had bilateral anophthalmia, the optic nerves not detectable by computed cranial tomography and magnetic resonance imaging, and the third child had bilateral microphthalmia and coloboma iridis." | 1.28 | New observations on midline defects: coincidence of anophthalmos, microphthalmos and cryptophthalmos with hypothalamic disorders. ( Bierich, JR; Christie, M; Heinrich, JJ; Martinez, AS, 1991) |
| "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) |
| "The first child had a large basal encephalocele, agenesis of the corpus callosum, mild optic atrophy in one eye, a retinal pigment epithelial defect in the other eye and bitemporal hemianopia; the second child had septo-optic dysplasia and the third child had Rieger's anomaly." | 1.26 | Ocular defects and short stature. ( Guyda, HJ; Little, JM; Polomeno, RC; Staudenmaier, C, 1980) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 11 (57.89) | 18.7374 |
| 1990's | 5 (26.32) | 18.2507 |
| 2000's | 2 (10.53) | 29.6817 |
| 2010's | 1 (5.26) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Singh, A | 1 |
| Arora, R | 1 |
| Singh, P | 1 |
| Kapoor, S | 1 |
| Bahillo, P | 1 |
| Cantero, T | 1 |
| Solís, P | 1 |
| Aragón, P | 1 |
| Gómez, S | 1 |
| Cambronero, R | 1 |
| Polomeno, RC | 1 |
| Staudenmaier, C | 1 |
| Guyda, HJ | 1 |
| Little, JM | 1 |
| Toriello, HV | 1 |
| Higgins, JV | 1 |
| Miller, T | 1 |
| Gündüz, K | 1 |
| Günalp, I | 1 |
| Erden, I | 1 |
| Monaghan, KG | 1 |
| Van Dyke, DL | 1 |
| Wiktor, A | 1 |
| Feldman, GL | 1 |
| Natacci, F | 1 |
| Pierri, M | 1 |
| Rossetti, M | 1 |
| Sala, M | 1 |
| Larizza, L | 1 |
| Bonnel, S | 1 |
| Dureau, P | 1 |
| LeMerrer, M | 1 |
| Dufier, JL | 1 |
| Benthem, LH | 1 |
| Bleeker-Wagemakers, EM | 1 |
| Delleman, JW | 1 |
| de Groot, WP | 1 |
| Pendergrass, TW | 1 |
| Gorlin, RJ | 1 |
| Cervenka, J | 1 |
| Moller, K | 1 |
| Horrobin, M | 1 |
| Witkop, CJ | 1 |
| Jones, KL | 1 |
| Smith, DW | 1 |
| Bierich, JR | 1 |
| Christie, M | 1 |
| Heinrich, JJ | 1 |
| Martinez, AS | 1 |
| Davenport, SL | 1 |
| Hefner, MA | 1 |
| Mitchell, JA | 1 |
| Stratton, RF | 1 |
| Parker, MW | 1 |
| McKeown, CA | 1 |
| Johnson, CP | 1 |
| Liberfarb, RM | 1 |
| Abdo, OP | 1 |
| Pruett, RC | 1 |
| Mollica, F | 1 |
| Pavone, L | 1 |
| Antener, I | 1 |
| Noël, B | 1 |
| Mottet, J | 1 |
| Nantois, Y | 1 |
| Quack, B | 1 |
| Arias, D | 1 |
| Passarge, E | 1 |
| Engle, MA | 1 |
| German, J | 1 |
1 review available for 2-propanol and Growth Disorders
| Article | Year |
|---|---|
Cytogenetic and clinical findings in a patient with a deletion of 16q23.1: first report of bilateral cataracts and a 16q deletion.
Topics: Abnormalities, Multiple; Autistic Disorder; Cataract; Child, Preschool; Chromosome Aberrations; Chro | 1997 |
18 other studies available for 2-propanol and Growth Disorders
| Article | Year |
|---|---|
Short syndrome-an expanding phenotype.
Topics: Adolescent; Consanguinity; Face; Fundus Oculi; Growth Disorders; Humans; Hypercalcemia; Iris; Male; | 2013 |
Hyper-IgM syndrome with CHARGE association.
Topics: Abnormalities, Multiple; Child, Preschool; Choanal Atresia; Coloboma; Cranial Nerve Diseases; Face; | 2003 |
Ocular defects and short stature.
Topics: Adolescent; Agenesis of Corpus Callosum; Child; Child, Preschool; Coloboma; Encephalocele; Eye Abnor | 1980 |
Provisionally unique autosomal recessive chondrodysplasia punctata syndrome.
Topics: Abnormalities, Multiple; Child; Child, Preschool; Chondrodysplasia Punctata; Coloboma; Face; Female; | 1993 |
Focal dermal hypoplasia (Goltz's syndrome).
Topics: Abnormalities, Multiple; Adolescent; Brain; Choroid; Coloboma; Cornea; Eye Abnormalities; Female; Fo | 1997 |
New case of the Richieri-Costa/Guion-Almeida syndrome.
Topics: Abnormalities, Multiple; Adolescent; Cleft Lip; Cleft Palate; Growth Disorders; Humans; Iris; Male; | 1999 |
SHORT syndrome: a case with high hyperopia and astigmatism.
Topics: Abnormalities, Multiple; Astigmatism; Child; Cornea; Corneal Opacity; Developmental Disabilities; Ey | 2000 |
[Profuse lentigo, little leopard syndrome].
Topics: Abnormalities, Multiple; Anus, Imperforate; Attention Deficit Disorder with Hyperactivity; Child; Cr | 1977 |
Congenital anomalies in children with Wilms' tumor: a new survey.
Topics: Child; Child, Preschool; Congenital Abnormalities; Female; Genitalia; Growth Disorders; Humans; Infa | 1976 |
Malformation syndromes. A selected miscellany.
Topics: Abnormalities, Multiple; Adolescent; Child; Child, Preschool; Chromosomes, Human, 6-12 and X; Dental | 1975 |
The Williams elfin facies syndrome. A new perspective.
Topics: Adolescent; Adult; Aortic Valve Stenosis; Child; Child, Preschool; Eyelids; Face; Female; Growth Dis | 1975 |
New observations on midline defects: coincidence of anophthalmos, microphthalmos and cryptophthalmos with hypothalamic disorders.
Topics: Abnormalities, Multiple; Anophthalmos; Anus, Imperforate; Coloboma; Congenital Hypothyroidism; Growt | 1991 |
The spectrum of clinical features in CHARGE syndrome.
Topics: Abnormalities, Multiple; Adolescent; Adult; Central Nervous System Diseases; Child, Preschool; Choan | 1986 |
Sibs with growth deficiency, delayed bone age, congenital hip dislocation, and iridocorneal abnormalities with glaucoma.
Topics: Abnormalities, Multiple; Body Height; Cornea; Female; Genes, Recessive; Glaucoma; Growth Disorders; | 1989 |
Ocular coloboma associated with a solitary maxillary central incisor and growth failure: manifestations of holoprosencephaly.
Topics: Abnormalities, Multiple; Cataract; Choroid; Coloboma; Eye Abnormalities; Growth Disorders; Humans; I | 1987 |
Short stature, mental retardation and ocular alterations in three siblings.
Topics: Adolescent; Cataract; Child; Chromosome Aberrations; Chromosome Disorders; Eye Diseases; Facial Expr | 1972 |
[Identification of the small submetacentric supernumerary chromosome in the cat's-eye syndrome].
Topics: Adult; Choroid; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 6-12 and X; Colobo | 1973 |
Human chromosomal deletion: two patients with the 4p- syndrome.
Topics: Abnormalities, Multiple; Autoradiography; Chromosome Aberrations; Chromosome Disorders; Chromosomes, | 1970 |