Literature DB >> 8480512

Fatal infantile encephalopathy with olivopontocerebellar hypoplasia and micrencephaly. Report of three siblings.

S Albrecht1, M C Schneider, J Belmont, D L Armstrong.   

Abstract

We report three siblings born with severe neonatal encephalopathy, manifested clinically by microcephaly, myoclonus, and muscular hypertonus. Karyotypic analyses and all biochemical investigations were unrevealing. All three patients died during infancy. Postmortem examination of the brain in one child disclosed severe neuronal loss in the inferior olives and the pontine nuclei. There was also severe hypoplasia of the cerebellum and micrencephaly. There was diffuse gliosis of the white matter in all areas of the brain. We believe this may represent a previously undescribed form of familial infantile encephalopathy with olivopontocerebellar hypoplasia.

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Year:  1993        PMID: 8480512     DOI: 10.1007/bf00334450

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


  23 in total

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Journal:  Arch Dis Child       Date:  1989-05       Impact factor: 3.791

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Journal:  Arch Dis Child       Date:  1989-01       Impact factor: 3.791

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Journal:  Clin Neuropathol       Date:  1990 Jan-Feb       Impact factor: 1.368

6.  Subtle cerebellar phenotype in mice homozygous for a targeted deletion of the En-2 homeobox.

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Journal:  Science       Date:  1991-03-08       Impact factor: 47.728

7.  Amyotrophic cerebellar hypoplasia: a specific form of infantile spinal atrophy.

Authors:  G A de León; W D Grover; C A D'Cruz
Journal:  Acta Neuropathol       Date:  1984       Impact factor: 17.088

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Journal:  J Neurol       Date:  1977-07-20       Impact factor: 4.849

9.  Congenital spongy degeneration of the brain (van Bogaert - Bertrand) associated with micrencephaly and ponto - cerebellar atrophy (contributions to the pathology of glial dystrophy of intrauterin origin).

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Journal:  Neuropadiatrie       Date:  1977-02

10.  Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalities.

Authors:  B N Harding; D B Dunger; D B Grant; M Erdohazi
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-03       Impact factor: 10.154

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Journal:  Brain       Date:  2010-10-15       Impact factor: 15.255

5.  Pontocerebellar hypoplasia type 2: a neuropathological update.

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6.  Posterior fossa in primary microcephaly: relationships between forebrain and mid-hindbrain size in 110 patients.

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Review 7.  Clinical and neuroimaging features as diagnostic guides in neonatal neurology diseases with cerebellar involvement.

Authors:  Jessica L Klein; Monica E Lemmon; Frances J Northington; Eugen Boltshauser; Thierry A G M Huisman; Andrea Poretti
Journal:  Cerebellum Ataxias       Date:  2016-01-13

Review 8.  What's new in pontocerebellar hypoplasia? An update on genes and subtypes.

Authors:  Tessa van Dijk; Frank Baas; Peter G Barth; Bwee Tien Poll-The
Journal:  Orphanet J Rare Dis       Date:  2018-06-15       Impact factor: 4.123

9.  TSEN54 missense variant in Standard Schnauzers with leukodystrophy.

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  9 in total

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