Morphological aspects of the development of hydrocephalus in a mouse mutant (SUMS/NP)
- 1 January 1987
- journal article
- research article
- Published by Springer Nature in Acta Neuropathologica
- Vol. 72 (3), 268-276
- https://doi.org/10.1007/bf00691100
Abstract
The SUMS/NP is a mouse mutant with a recessive gene for congenital hydrocephalus. The condition is detectable outwardly at 3 days after birth and affected animals die soon after weaning. The heads of fetuses from 14 to 20 days gestation and at 1, 4, 5, 12 and 18 days after birth have been sectioned for light microscopy and the volume of the lateral ventricles measured in all but the three oldest ages. At 16 days gestation and earlier all fetuses had a relatively large lateral ventricle volume. Hydrocephalus was first detected from volume measurements at 18 days gestation and generally became progressively more severe with age. Hydrocephalic animals, in addition to lateral and third ventricle dilatation, always showed a reduction in the cross-sectional area of the cerebral aqueduct or a total absence of the aqueduct. All hydrocephalics, with the exception of two fetuses, also had cystic cavitation of the forebrain around the lateral ventricles. Electron microscopy of animals with a reduced aqueduct showed the ventral part to be absent in hydrocephalics.This publication has 15 references indexed in Scilit:
- Cerebrospinal fluid pressure and resistance to absorption during development in normal and hydrocephalic mutant miceExperimental Neurology, 1985
- The Development of Congenital Hydrocephalus in the MouseEuropean Journal of Pediatric Surgery, 1984
- The limitation of pulsatile flow through the aqueduct of sylvius as a cause of hydrocephalusJournal of the Neurological Sciences, 1979
- Brain development in hydrocephalic-polydactyl, a recessive pleiotropic mutant in the mouseVirchows Archiv, 1977
- Pathogenesis of aqueductal occlusion in congenital murine hydrocephalusJournal of Neurosurgery, 1976
- Developmental morphology of the subarachnoid space and contiguous structures in the mouseJournal of Anatomy, 1975
- Aqueductal stenosis as the cause of hydrocephalus in mice fed the substituted hydrazine, cuprizoneExperimental and Molecular Pathology, 1970
- The inheritance and pathogenesis of hydrocephalus‐3 in the mouseThe Journal of Pathology and Bacteriology, 1961
- HEREDITARY STENOSIS OF THE AQUEDUCT OF SYLVIUS AS A CAUSE OF CONGENITAL HYDROCEPHALUSBrain, 1949
- Two new mutant genes in the house mouseJournal of Genetics, 1943