Literature DB >> 6475488

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

G A de León, W D Grover, C A D'Cruz.   

Abstract

Lower motor neuron degeneration, cerebellar hypoplasia, atrophy of pons, olives, and cerebellum, sclerosis of thalamus and pallidum, and deficient myelination were found in a 2-months-old baby with laryngeal paralysis, mental retardation, progressive amyotrophy, and slow nerve conduction velocity. Such changes seem characteristic of an unusual syndrome previously referred to as "cerebellar hypoplasia in Werdnig-Hoffmann disease", or "anterior horn cell disease with pontocerebellar hypoplasia". Although the pathologic changes in lower motor neurons are indistinguishable from those in other cases of infantile spinal muscular atrophy, the consistent reproducibility of a complex pathologic pattern suggests that this is probably a manifestation of a separate disease process. The term "amyotrophic cerebellar hypoplasia" (ACH) is a convenient designation for the syndrome.

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Mesh:

Year:  1984        PMID: 6475488     DOI: 10.1007/bf00687334

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


  10 in total

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  10 in total
  9 in total

1.  Infantile cerebello-optic atrophy. Neuropathology of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome).

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5.  Pontocerebellar hypoplasia type 1: clinical spectrum and relevance of EXOSC3 mutations.

Authors:  Sabine Rudnik-Schöneborn; Jan Senderek; Joanna C Jen; Gunnar Houge; Pavel Seeman; Alena Puchmajerová; Luitgard Graul-Neumann; Ulrich Seidel; Rudolf Korinthenberg; Janbernd Kirschner; Jürgen Seeger; Monique M Ryan; Francesco Muntoni; Maja Steinlin; Laszlo Sztriha; Jaume Colomer; Christoph Hübner; Knut Brockmann; Lionel Van Maldergem; Manuel Schiff; Andreas Holzinger; Peter Barth; William Reardon; Michael Yourshaw; Stanley F Nelson; Thomas Eggermann; Klaus Zerres
Journal:  Neurology       Date:  2013-01-02       Impact factor: 9.910

Review 6.  Classification, diagnosis and potential mechanisms in pontocerebellar hypoplasia.

Authors:  Yasmin Namavar; Peter G Barth; Bwee Tien Poll-The; Frank Baas
Journal:  Orphanet J Rare Dis       Date:  2011-07-12       Impact factor: 4.123

7.  Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration.

Authors:  Jijun Wan; Michael Yourshaw; Hafsa Mamsa; Sabine Rudnik-Schöneborn; Manoj P Menezes; Ji Eun Hong; Derek W Leong; Jan Senderek; Michael S Salman; David Chitayat; Pavel Seeman; Arpad von Moers; Luitgard Graul-Neumann; Andrew J Kornberg; Manuel Castro-Gago; María-Jesús Sobrido; Masafumi Sanefuji; Perry B Shieh; Noriko Salamon; Ronald C Kim; Harry V Vinters; Zugen Chen; Klaus Zerres; Monique M Ryan; Stanley F Nelson; Joanna C Jen
Journal:  Nat Genet       Date:  2012-04-29       Impact factor: 38.330

8.  Pontocerebellar hypoplasia type 2: a neuropathological update.

Authors:  Peter G Barth; Eleonora Aronica; Linda de Vries; Peter G J Nikkels; Wiep Scheper; Jeroen J Hoozemans; Bwe-Tien Poll-The; Dirk Troost
Journal:  Acta Neuropathol       Date:  2007-07-20       Impact factor: 17.088

9.  EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations.

Authors:  Veerle Rc Eggens; Peter G Barth; Jikke-Mien F Niermeijer; Jonathan N Berg; Niklas Darin; Abhijit Dixit; Joel Fluss; Nicola Foulds; Darren Fowler; Tibor Hortobágyi; Thomas Jacques; Mary D King; Periklis Makrythanasis; Adrienn Máté; James A R Nicoll; Declan O'Rourke; Sue Price; Andrew N Williams; Louise Wilson; Mohnish Suri; Laszlo Sztriha; Marit B Dijns-de Wissel; Mia T van Meegen; Fred van Ruissen; Eleonora Aronica; Dirk Troost; Charles Blm Majoie; Henk A Marquering; Bwee Tien Poll-Thé; Frank Baas
Journal:  Orphanet J Rare Dis       Date:  2014-02-13       Impact factor: 4.123

  9 in total

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