Literature DB >> 9120454

Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy.

R M Chalmers1, P Riordan-Eva, N W Wood.   

Abstract

Three siblings are reported with childhood onset hereditary motor and sensory neuropathy (HMSN) and adult onset optic atrophy. Electrophysiological studies showed an axonal neuropathy and dysfunction of the retinal ganglion cells or optic nerve. The presumed mode of inheritance is autosomal recessive. This is the second family in which autosomal recessive inheritance of HMSN and optic atrophy (HMSN type VI) has been described, and the first in which electrophysiological studies have been reported.

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Year:  1997        PMID: 9120454      PMCID: PMC1074097          DOI: 10.1136/jnnp.62.4.385

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  7 in total

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Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1991       Impact factor: 5.270

2.  Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy.

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Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-02       Impact factor: 10.154

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Review 4.  From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins.

Authors:  A E Harding
Journal:  Brain       Date:  1995-06       Impact factor: 13.501

Review 5.  Optic atrophy, hearing loss, and peripheral neuropathy.

Authors:  K Hagemoser; J Weinstein; G Bresnick; R Nellis; S Kirkpatrick; R M Pauli
Journal:  Am J Med Genet       Date:  1989-05

6.  Charcot-Marie-Tooth disease with primary optic atrophy; report of a case.

Authors:  W F HOYT
Journal:  Arch Ophthalmol       Date:  1960-12

7.  Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis.

Authors:  H Eiberg; B Kjer; P Kjer; T Rosenberg
Journal:  Hum Mol Genet       Date:  1994-06       Impact factor: 6.150

  7 in total
  5 in total

Review 1.  The neuro-ophthalmology of mitochondrial disease.

Authors:  J Alexander Fraser; Valérie Biousse; Nancy J Newman
Journal:  Surv Ophthalmol       Date:  2010-05-14       Impact factor: 6.048

2.  PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementation.

Authors:  Viorica Chelban; Matthew P Wilson; Jodi Warman Chardon; Jana Vandrovcova; M Natalia Zanetti; Eleni Zamba-Papanicolaou; Stephanie Efthymiou; Simon Pope; Maria R Conte; Giancarlo Abis; Yo-Tsen Liu; Eloise Tribollet; Nourelhoda A Haridy; Juan A Botía; Mina Ryten; Paschalis Nicolaou; Anna Minaidou; Kyproula Christodoulou; Kristin D Kernohan; Alison Eaton; Matthew Osmond; Yoko Ito; Pierre Bourque; James E C Jepson; Oscar Bello; Fion Bremner; Carla Cordivari; Mary M Reilly; Martha Foiani; Amanda Heslegrave; Henrik Zetterberg; Simon J R Heales; Nicholas W Wood; James E Rothman; Kym M Boycott; Philippa B Mills; Peter T Clayton; Henry Houlden
Journal:  Ann Neurol       Date:  2019-07-01       Impact factor: 10.422

Review 3.  Inherited mitochondrial optic neuropathies.

Authors:  P Yu-Wai-Man; P G Griffiths; G Hudson; P F Chinnery
Journal:  J Med Genet       Date:  2008-11-10       Impact factor: 6.318

4.  Genetic Spectrum and Characteristics of Hereditary Optic Neuropathy in Taiwan.

Authors:  Chao-Wen Lin; Ching-Wen Huang; Allen Chilun Luo; Yuh-Tsyr Chou; Yu-Shu Huang; Pei-Lung Chen; Ta-Ching Chen
Journal:  Genes (Basel)       Date:  2021-08-31       Impact factor: 4.096

5.  Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophy.

Authors:  Arianna Tucci; Yo-Tsen Liu; Elisabeth Preza; Robert D S Pitceathly; Annapurna Chalasani; Vincent Plagnol; John M Land; Daniah Trabzuni; Mina Ryten; Zane Jaunmuktane; Mary M Reilly; Sebastian Brandner; Iain Hargreaves; John Hardy; Andrew B Singleton; Andrey Y Abramov; Henry Houlden
Journal:  J Neurol Neurosurg Psychiatry       Date:  2013-11-06       Impact factor: 10.154

  5 in total

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