CT and MRI of the Brain in Inherited Neurometabolic Disorders
- 1 April 1992
- journal article
- review article
- Published by SAGE Publications in Journal of Child Neurology
- Vol. 7 (1_suppl) , S112-S131
- https://doi.org/10.1177/08830738920070011611
Abstract
The incidence of many autosomal recessive neurometabolic disorders is very high in Saudi Arabia, probably as a result of the frequency of consanguineous marriages. Because our hospital is the main referral center for the entire Kingdom, we examine a large number of patients who have a wide spectrum of neurometabolic disorders. We add our experience and review the world literature. Though a specific diagnosis is radiologically possible in a few disorders, the diagnosis must always be verified biochemically. When the patient is referred from a pediatric neurologist with the diagnosis of neurometabolic disorder, the aim of the neuroradiologist is to determine the amount of brain damage present and to follow the response to given therapy. When the patient is referred with a nonspecific diagnosis, such as delayed development, the aim is to suggest the possibility of a neurometabolic disorder and to initiate further evaluation including possible therapy and genetic counseling. (J Child Neurol 1992;7(Suppl):S112-S131.)Keywords
This publication has 58 references indexed in Scilit:
- MR imaging of the various stages of normal myelination during the first year of lifeNeuroradiology, 1990
- Normal maturation of the neonatal and infant brain: MR imaging at 1.5 T.Radiology, 1988
- The value of computed tomography in patients with mucopolysaccharidosisNeuroradiology, 1987
- CRANIAL COMPUTERIZED TOMOGRAPHY IN PHENYLKETONURIA1Neuropediatrics, 1981
- Computed tomography studies on patients with mucopolysaccharidosesNeuroradiology, 1981
- Computed Tomography in White-Matter DiseaseRadiology, 1979
- Computerized cranial tomography in cerebral diseases of white matterNeurology, 1978
- Computed tomography in neurodegenerative disorders in childhoodNeuroradiology, 1978
- Computerized tomography in demyelinating disease of the youngNeurology, 1977
- Über Ausscheidung von Phenylbrenztraubensäure in den Harn als Stoffwechselanomalie in Verbindung mit Imbezillität.Hoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1934