Literature DB >> 185990

Acromutilating, paralyzing neuropathy with corneal ulceration in Navajo children.

O Appenzeller, M Kornfeld, R Snyder.   

Abstract

Four Navajo children had a mutilating neuropathy with severe motor involvement. The disorder appears to be recessively inherited and is present from the earliest observable age. Manifestations include severe anesthesia, corneal ulceration, painless fractures, acral mutilation, and weakness. Mental function is normal. Sural nerves are practically devoid of myelinated fibers that show no evidence of regeneration. Unmyelinated axons show degenerative and regenerative morphologic and histometric features. Onion bulb formation is absent. We believe this neuropathy is a distinct clinical entity.

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Mesh:

Year:  1976        PMID: 185990     DOI: 10.1001/archneur.1976.00500110001001

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  8 in total

1.  Hand involvement in Navajo neurohepatopathy: a case report.

Authors:  Tahseen A Cheema; Scott Swanson
Journal:  Hand (N Y)       Date:  2010-11-19

2.  [Quantitative and electron microscope study of the nerve in seven cases of sporadic idiopathic sensory neuropathy (author's transl)].

Authors:  A Guimaraes; J J Hauw; R Escourolle
Journal:  Acta Neuropathol       Date:  1979-04-12       Impact factor: 17.088

3.  Navajo neurohepatopathy is caused by a mutation in the MPV17 gene.

Authors:  Charalampos L Karadimas; Tuan H Vu; Stephen A Holve; Penelope Chronopoulou; Catarina Quinzii; Stanley D Johnsen; Janice Kurth; Elizabeth Eggers; Lluis Palenzuela; Kurenai Tanji; Eduardo Bonilla; Darryl C De Vivo; Salvatore DiMauro; Michio Hirano
Journal:  Am J Hum Genet       Date:  2006-06-28       Impact factor: 11.025

Review 4.  Genetic pain loss disorders.

Authors:  Annette Lischka; Petra Lassuthova; Arman Çakar; Christopher J Record; Jonas Van Lent; Jonathan Baets; Maike F Dohrn; Jan Senderek; Angelika Lampert; David L Bennett; John N Wood; Vincent Timmerman; Thorsten Hornemann; Michaela Auer-Grumbach; Yesim Parman; Christian A Hübner; Miriam Elbracht; Katja Eggermann; C Geoffrey Woods; James J Cox; Mary M Reilly; Ingo Kurth
Journal:  Nat Rev Dis Primers       Date:  2022-06-16       Impact factor: 65.038

5.  Hereditary sensory neuropathy. Nociceptive loss and acral mutilation in pointer dogs: canine hereditary sensory neuropathy.

Authors:  J F Cummings; A de Lahunta; K G Braund; W J Mitchell
Journal:  Am J Pathol       Date:  1983-07       Impact factor: 4.307

6.  Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout mice.

Authors:  Carlo Viscomi; Antonella Spinazzola; Marco Maggioni; Erika Fernandez-Vizarra; Valeria Massa; Claudio Pagano; Roberto Vettor; Marina Mora; Massimo Zeviani
Journal:  Hum Mol Genet       Date:  2008-09-24       Impact factor: 6.150

7.  MPV17-related hepatocerebral mitochondrial DNA depletion syndrome (MPV17-NNH) revisited.

Authors:  Clifford Qualls; Mario Kornfeld; Nancy Joste; Abdul-Mehdi Ali; Otto Appenzeller
Journal:  eNeurologicalSci       Date:  2016-01-28

8.  A novel MPV17 gene mutation in a Saudi infant causing fatal progressive liver failure.

Authors:  Ahmed Al Sarkhy; Areej Al-Sunaid; Ahmad Abdullah; Majid AlFadhel; Wafa Eiyad
Journal:  Ann Saudi Med       Date:  2014 Mar-Apr       Impact factor: 1.526

  8 in total

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