glutaric acid has been researched along with Cerebral Palsy in 6 studies
glutaric acid: RN given refers to parent cpd
glutaric acid : An alpha,omega-dicarboxylic acid that is a linear five-carbon dicarboxylic acid.
Cerebral Palsy: A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7)
| Excerpt | Relevance | Reference |
|---|---|---|
| "In a male infant with macrocephaly and dystonic cerebral palsy glutaric aciduria type I was detected by analysis of urine for organic acids." | 7.68 | [Macrocephaly and dystonic cerebral palsy in a child with type I glutaric aciduria]. ( Christensen, E; Colombo, JP; Plöchl, E; Weiss-Wichert, P; Wenger, E, 1991) |
| "In a male infant with macrocephaly and dystonic cerebral palsy glutaric aciduria type I was detected by analysis of urine for organic acids." | 3.68 | [Macrocephaly and dystonic cerebral palsy in a child with type I glutaric aciduria]. ( Christensen, E; Colombo, JP; Plöchl, E; Weiss-Wichert, P; Wenger, E, 1991) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 4 (66.67) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hauser, SE | 1 |
| Peters, H | 1 |
| Ulrich, T | 1 |
| Monavari, AA | 1 |
| Naughten, ER | 1 |
| Plöchl, E | 1 |
| Christensen, E | 1 |
| Colombo, JP | 1 |
| Weiss-Wichert, P | 1 |
| Wenger, E | 1 |
| Morton, DH | 1 |
| Bennett, MJ | 1 |
| Seargeant, LE | 1 |
| Nichter, CA | 1 |
| Kelley, RI | 1 |
| Stutchfield, P | 1 |
| Edwards, MA | 1 |
| Gray, RG | 1 |
| Crawley, P | 1 |
| Green, A | 1 |
6 other studies available for glutaric acid and Cerebral Palsy
| Article | Year |
|---|---|
Glutaric aciduria type 1: an underdiagnosed cause of encephalopathy and dystonia-dyskinesia syndrome in children.
Topics: Amino Acid Metabolism, Inborn Errors; Cerebral Palsy; Child, Preschool; Diagnosis, Differential; Dys | 1998 |
Linking an Amish hereditary disease with cerebral palsy, a pediatrician challenges a dark inheritance.
Topics: Cerebral Palsy; Child; Christianity; Ethnicity; Founder Effect; Genetic Carrier Screening; Genetic L | 1997 |
Prevention of cerebral palsy in glutaric aciduria type 1 by dietary management.
Topics: Adolescent; Adult; Biomarkers; Cerebral Palsy; Child; Family Health; Glutarates; Humans; Magnetic Re | 2000 |
[Macrocephaly and dystonic cerebral palsy in a child with type I glutaric aciduria].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Cephalometry; Cerebral Palsy; Dietary Proteins; G | 1991 |
Glutaric aciduria type I: a common cause of episodic encephalopathy and spastic paralysis in the Amish of Lancaster County, Pennsylvania.
Topics: Acute Disease; Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Cells, Cultured; Cerebral Pa | 1991 |
Glutaric aciduria type I misdiagnosed as Leigh's encephalopathy and cerebral palsy.
Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Cerebral Palsy; Child; Child, Presc | 1985 |