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Literature DB >> 6880614

Pachygyria and congenital nephrosis disorder of migration and neuronal orientation.

Abstract

A case of pachygyria with associated nephrosis has been studied. Several microscopic abnormalities have been identified: cytoarchitectonic disorders including neuronal ectopies in the molecular layer and in the meninges, improperly oriented neurons shown with Golgi stain, fetal aspect of inferior olives. The mechanism of the disorder of migration and neuronal and dendritic orientation are discussed. The significance of the association of microcephaly and nephrosis is also reviewed in light of recent literature.

Entities: Disease

Mesh：

Year: 1983 PMID： 6880614 DOI： 10.1007/bf00685358

Source DB: PubMed Journal: Acta Neuropathol ISSN： 0001-6322 Impact factor: 17.088

13 in total

1. Pachygyria.

Authors: L CROME
Journal: J Pathol Bacteriol Date: 1956-04

2. [Familial microcephalies due to cerebral malformation. Anatomical and clinical study].

Authors: O Robain; G Lyon
Journal: Acta Neuropathol Date: 1972 Impact factor: 17.088

3. Congenital microcephaly with hiatus hernia and nephrotic syndrome in two sibs.

Authors: W H Galloway; A P Mowat
Journal: J Med Genet Date: 1968-12 Impact factor: 6.318

4. The subpial granular layer of the foetal cerebral cortex in man. Its ontogeny and significance in congenital cortical malformations.

Authors: A Brun
Journal: Acta Pathol Microbiol Scand Date: 1965

5. Radial neuronal assemblies, ectopia and necrosis of developing cortex: a case analysis.

Authors: V S Caviness; P Evrard; G Lyon
Journal: Acta Neuropathol Date: 1978-01-19 Impact factor: 17.088

6. Identification of Cajal-Retzius cells in immature rodent cerebral cortex: a combined Golgi--EM study.

Authors: N König; J P Hornung; H Van der Loos
Journal: Neurosci Lett Date: 1981-12-23 Impact factor: 3.046

7. Heredity in the congenital nephrotic syndrome. A genetic study of 57 finnish FAMILIES WITH A REVIEW OF REPORTED CASES.

Authors: R Norio
Journal: Ann Paediatr Fenn Date: 1966

8. Pattern and field in cortical structure: the rabbit.

Authors: A Globus; A B Scheibel
Journal: J Comp Neurol Date: 1967-10 Impact factor: 3.215

9. Lissencephaly and Pachygyria: an architectonic and topographical analysis.

Authors: R M Stewart; D P Richman; V S Caviness
Journal: Acta Neuropathol Date: 1975 Impact factor: 17.088

10. Experimental studies on cerebellar foliation. I. A qualitative morphological analysis of cerebellar fissuration defects after neonatal treatment with 6-OHDA in the rat.

Authors: J Sievers; U Mangold; M Berry; C Allen; H G Schlossberger
Journal: J Comp Neurol Date: 1981-12-20 Impact factor: 3.215

13 in total

1. Clinical quiz. Congenital nephrotic syndrome, microcephaly, brain malformations and diaphragmatic abnormality associated with histological features of diffuse mesangial sclerosis.

Authors: O Koskimies; H Sariola; C Holmberg; J Rapola
Journal: Pediatr Nephrol Date: 1991-07 Impact factor: 3.714

Review 10. Congenital nephrotic syndrome.

Authors: J Rapola
Journal: Pediatr Nephrol Date: 1987-07 Impact factor: 3.714

Pachygyria and congenital nephrosis disorder of migration and neuronal orientation.

1. Pachygyria.

2. [Familial microcephalies due to cerebral malformation. Anatomical and clinical study].

3. Congenital microcephaly with hiatus hernia and nephrotic syndrome in two sibs.

4. The subpial granular layer of the foetal cerebral cortex in man. Its ontogeny and significance in congenital cortical malformations.

5. Radial neuronal assemblies, ectopia and necrosis of developing cortex: a case analysis.

6. Identification of Cajal-Retzius cells in immature rodent cerebral cortex: a combined Golgi--EM study.

7. Heredity in the congenital nephrotic syndrome. A genetic study of 57 finnish FAMILIES WITH A REVIEW OF REPORTED CASES.

8. Pattern and field in cortical structure: the rabbit.

9. Lissencephaly and Pachygyria: an architectonic and topographical analysis.

10. Experimental studies on cerebellar foliation. I. A qualitative morphological analysis of cerebellar fissuration defects after neonatal treatment with 6-OHDA in the rat.

1. Clinical quiz. Congenital nephrotic syndrome, microcephaly, brain malformations and diaphragmatic abnormality associated with histological features of diffuse mesangial sclerosis.

2. Muscular dystonia and athetosis in six patients with congenital nephrotic syndrome of the Finnish type (NPHS1).

3. Inverted neurons in agyria. A Golgi study of a case with abnormal chromosome 17.

4. Cortical dysplasia associated with massive ectopia of neurons and glial cells within the subarachnoid space.

5. Congenital microcephaly and infantile nephrotic syndrome--a case report.

6. Microcephaly and early-onset nephrotic syndrome--confusion in Galloway-Mowat syndrome.

7. Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome.

8. Congenital microcephaly, infantile spasms, psychomotor retardation, and nephrotic syndrome in two sibs.

9. Shaking rat Kawasaki (SRK): a new neurological mutant rat in the Wistar strain.

Review 10. Congenital nephrotic syndrome.