Literature DB >> 3407465

Neuropathology of congenital hydrocephalus in the SUMS/NP mouse.

J E Bruni1, M R del Bigio, E R Cardoso, T V Persaud.   

Abstract

The neuropathology of congenital hydrocephalus in SUMS/NP mice was investigated in this study. Hydrocephalus occurred with an incidence of 16.5% and was evident in the form of an enlarged head soon after birth. The condition was progressive; affected mice gradually became noticeably smaller than normals, acquired functional disturbances and died before ever breeding. Hydrocephalic mice exhibited enormous dilatation of the lateral ventricles, thinning of the cortex and compression and distortion of the diencephalon and striatum. Examination of the midbrain in these animals revealed that the proximal cerebral aqueduct was diminished in size, occluded or absent. Evidence of its anomalous development was seen as early as day 15 of foetal development. This is in substantial agreement with previous reports on this strain. Although the mechanism by which this occurs is still unknown, abnormal development of the adjoining diencephalon and/or rostral midbrain is likely to be involved.

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Year:  1988        PMID: 3407465     DOI: 10.1007/bf01401981

Source DB:  PubMed          Journal:  Acta Neurochir (Wien)        ISSN: 0001-6268            Impact factor:   2.216


  24 in total

1.  Brain development in hydrocephalic-polydactyl, a recessive pleiotropic mutant in the mouse.

Authors:  J H Bryan; R L Hughes; T J Bates
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1977-06-23

2.  Hydrocephalus, a Hereditary Character in the House Mouse.

Authors:  F H Clark
Journal:  Proc Natl Acad Sci U S A       Date:  1932-11       Impact factor: 11.205

3.  The developmental effects of congenital hydrocephalus (ch) in the mouse.

Authors:  M C Green
Journal:  Dev Biol       Date:  1970-12       Impact factor: 3.582

4.  Congenital hydrocephalus and the basal cell nevus syndrome.

Authors:  B A Lycka; V R Chichak
Journal:  Can Med Assoc J       Date:  1985-05-01       Impact factor: 8.262

Review 5.  Ependyma: normal and pathological. A review of the literature.

Authors:  J E Bruni; M R Del Bigio; R E Clattenburg
Journal:  Brain Res       Date:  1985-04       Impact factor: 3.252

6.  Cerebrospinal fluid pressure and resistance to absorption during development in normal and hydrocephalic mutant mice.

Authors:  H C Jones
Journal:  Exp Neurol       Date:  1985-10       Impact factor: 5.330

7.  Renal dysplasia and chondrodysplasia in the ch hydrocephalic mouse: a cellular model of defective differentiation and organization.

Authors:  R R Richardson; M G Reyes
Journal:  Mt Sinai J Med       Date:  1984-04

8.  Morphological aspects of the development of hydrocephalus in a mouse mutant (SUMS/NP).

Authors:  H C Jones; S Dack; C Ellis
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

9.  Micro- and macrovascular changes as the direct cause of parenchymal destruction in congenital murine hydrocephalus.

Authors:  M Wozniak; D G McLone; A J Raimondi
Journal:  J Neurosurg       Date:  1975-11       Impact factor: 5.115

10.  X-linked hydrocephalus.

Authors:  R I Kuzniecky; G V Watters; L Watters; K Meagher-Villemure
Journal:  Can J Neurol Sci       Date:  1986-11       Impact factor: 2.104

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  1 in total

1.  Intracerebroventricular antisense knockdown of G alpha i2 results in ciliary stasis and ventricular dilatation in the rat.

Authors:  Kati S Mönkkönen; Juhana M Hakumäki; Robert A Hirst; Riitta A Miettinen; Christopher O'Callaghan; Pekka T Männistö; Jarmo T Laitinen
Journal:  BMC Neurosci       Date:  2007-04-12       Impact factor: 3.288

  1 in total

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