Literature DB >> 10932274

Hereditary motor and sensory neuropathy with myelin folding and juvenile onset glaucoma.

T Kiwaki1, F Umehara, H Takashima, M Nakagawa, K Kamimura, N Kashio, Y Sakamoto, K Unoki, Y Nobuhara, K Michizono, O Watanabe, H Arimura, M Osame.   

Abstract

OBJECTIVE: We describe three patients from a family with motor and sensory neuropathy accompanied by open-angle glaucoma.
BACKGROUND: Autosomal recessive demyelinating hereditary motor and sensory neuropathies (HMSN) include different disorders. To our knowledge, autosomal recessive HMSN has not been associated with juvenile onset glaucoma.
METHODS: Sural nerve pathology of the three patients were examined, and genetic analysis of the family was performed. RESULT: - The most prominent pathologic finding was a highly unusual myelin abnormality consisting of irregular redundant loops and folding of the myelin sheath. The family survey supports autosomal recessive inheritance. The molecular analysis failed to demonstrate either linkage of the disease to MPZ gene, PMP22 gene, Cx32 gene, orEGR2 gene. Analysis did not establish linkage of the disease to the locus of CMT4A, 4B, and 4C genes.
CONCLUSION: The present cases may represent a new type of HMSN accompanied by juvenile onset glaucoma.

Entities:  

Mesh:

Year:  2000        PMID: 10932274     DOI: 10.1212/wnl.55.3.392

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  6 in total

Review 1.  Juvenile-onset open-angle glaucoma - A clinical and genetic update.

Authors:  Harathy Selvan; Shikha Gupta; Janey L Wiggs; Viney Gupta
Journal:  Surv Ophthalmol       Date:  2021-09-16       Impact factor: 6.197

2.  Loss of the inactive myotubularin-related phosphatase Mtmr13 leads to a Charcot-Marie-Tooth 4B2-like peripheral neuropathy in mice.

Authors:  Fred L Robinson; Ingrid R Niesman; Kristina K Beiswenger; Jack E Dixon
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-18       Impact factor: 11.205

3.  Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma.

Authors:  H Azzedine; A Bolino; T Taïeb; N Birouk; M Di Duca; A Bouhouche; S Benamou; A Mrabet; T Hammadouche; T Chkili; R Gouider; R Ravazzolo; A Brice; J Laporte; E LeGuern
Journal:  Am J Hum Genet       Date:  2003-04-08       Impact factor: 11.025

4.  Whole-exome sequencing in patients with inherited neuropathies: outcome and challenges.

Authors:  Maria Schabhüttl; Thomas Wieland; Jan Senderek; Jonathan Baets; Vincent Timmerman; Peter De Jonghe; Mary M Reilly; Karl Stieglbauer; Eva Laich; Reinhard Windhager; Wolfgang Erwa; Slave Trajanoski; Tim M Strom; Michaela Auer-Grumbach
Journal:  J Neurol       Date:  2014-03-15       Impact factor: 4.849

5.  Charcot-Marie-Tooth 4B2 caused by a novel mutation in the MTMR13/SBF2 gene in two related Portuguese families.

Authors:  Luís Negrão; Luciano Almendra; Joana Ribeiro; Anabela Matos; Argemiro Geraldo; Jorge Pinto-Basto
Journal:  Acta Myol       Date:  2014-12

6.  An In Vitro Model of Charcot-Marie-Tooth Disease Type 4B2 Provides Insight Into the Roles of MTMR13 and MTMR2 in Schwann Cell Myelination.

Authors:  Danielle C Robinson; Anna E Mammel; Anne M Logan; Aubree A Larson; Eric J Schmidt; Alec F Condon; Fred L Robinson
Journal:  ASN Neuro       Date:  2018 Jan-Dec       Impact factor: 4.146

  6 in total

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