Literature DB >> 9219740

Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family.

P De Jonghe1, V Timmerman, D FitzPatrick, P Spoelders, J J Martin, C Van Broeckhoven.   

Abstract

BACKGROUND: Charcot-Marie-Tooth disease type 2 (CMT2) or hereditary motor and sensory neuropathy type II (HMSN II) is an inherited axonal neuropathy of the peripheral nervous system. Three autosomal dominant CMT2 loci have been located on chromosomes 1p35-p36 (CMT2A), 3q13-q22 (CMT2B), and 7p14 (CMT2D) indicating that CMT2 is a genetically heterogeneous disorder.
METHODS: A CMT2 family was examined for linkage to the CMT2A, CMT2B, and CMT2D loci using short tandem repeat polymorphisms.
RESULTS: Suggestive evidence for linkage to 3q13-q22 was found. Recombinations occurred with markers D3S1769 and D3S1267 indicating that the CMT2B locus is located distal to D3S1267 and resides in an interval of 25 cM. Some patients in this family have pronounced sensory disturbances leading to poorly healing ulcerations.
CONCLUSIONS: These unusual sensory signs for CMT were also noted in the only other CMT2B family reported so far, suggesting a distinct clinical phenotype for CMT2B. Exclusion of the locus for hereditary sensory neuropathy type I (HSN I) on chromosome 9q22 indicates that HSN I with mild motor symptoms and CMT2 with prominent sensory abnormalities are not allelic.

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Year:  1997        PMID: 9219740      PMCID: PMC1074138          DOI: 10.1136/jnnp.62.6.570

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


  14 in total

1.  Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B.

Authors:  J M Vance; M C Speer; J M Stajich; S West; C Wolpert; P Gaskell; F Lennon; R M Tim; M Rozear; K B Othmane
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

2.  Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D).

Authors:  V Ionasescu; C Searby; V C Sheffield; T Roklina; D Nishimura; R Ionasescu
Journal:  Hum Mol Genet       Date:  1996-09       Impact factor: 6.150

3.  Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and Xq13.

Authors:  V Timmerman; P De Jonghe; P Spoelders; S Simokovic; A Löfgren; E Nelis; J Vance; J J Martin; C Van Broeckhoven
Journal:  Neurology       Date:  1996-05       Impact factor: 9.910

4.  A comprehensive genetic map of the human genome based on 5,264 microsatellites.

Authors:  C Dib; S Fauré; C Fizames; D Samson; N Drouot; A Vignal; P Millasseau; S Marc; J Hazan; E Seboun; M Lathrop; G Gyapay; J Morissette; J Weissenbach
Journal:  Nature       Date:  1996-03-14       Impact factor: 49.962

5.  Faster sequential genetic linkage computations.

Authors:  R W Cottingham; R M Idury; A A Schäffer
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

6.  The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3.

Authors:  G A Nicholson; J L Dawkins; I P Blair; M L Kennerson; M J Gordon; A K Cherryson; J Nash; T Bananis
Journal:  Nat Genet       Date:  1996-05       Impact factor: 38.330

7.  Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity.

Authors:  K Ben Othmane; L T Middleton; L J Loprest; K M Wilkinson; F Lennon; M P Rozear; J M Stajich; P C Gaskell; A D Roses; M A Pericak-Vance
Journal:  Genomics       Date:  1993-08       Impact factor: 5.736

8.  Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families.

Authors:  G Nicholson; J Nash
Journal:  Neurology       Date:  1993-12       Impact factor: 9.910

9.  The clinical features of hereditary motor and sensory neuropathy types I and II.

Authors:  A E Harding; P K Thomas
Journal:  Brain       Date:  1980-06       Impact factor: 13.501

10.  Genetic heterogeneity in Charcot-Marie-Tooth neuropathy type 2.

Authors:  R Yoshioka; P J Dyck; P F Chance
Journal:  Neurology       Date:  1996-02       Impact factor: 9.910

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  10 in total

1.  A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene.

Authors:  I V Mersiyanova; A V Perepelov; A V Polyakov; V F Sitnikov; E L Dadali; R B Oparin; A N Petrin; O V Evgrafov
Journal:  Am J Hum Genet       Date:  2000-06-07       Impact factor: 11.025

Review 2.  A review of genetic counseling for Charcot Marie Tooth disease (CMT).

Authors:  Carly E Siskind; Seema Panchal; Corrine O Smith; Shawna M E Feely; Joline C Dalton; Alice B Schindler; Karen M Krajewski
Journal:  J Genet Couns       Date:  2013-04-21       Impact factor: 2.537

3.  Hereditary sensory neuropathy type I: haplotype analysis shows founders in southern England and Europe.

Authors:  G A Nicholson; J L Dawkins; I P Blair; M Auer-Grumbach; S B Brahmbhatt; D J Hulme
Journal:  Am J Hum Genet       Date:  2001-07-27       Impact factor: 11.025

Review 4.  Molecular genetics of hereditary sensory neuropathies.

Authors:  Michaela Auer-Grumbach; Barbara Mauko; Piet Auer-Grumbach; Thomas R Pieber
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

5.  Axonal Charcot-Marie-Tooth disease and the neurofilament light gene (NF-L)

Authors:  J R Lupski
Journal:  Am J Hum Genet       Date:  2000-06-07       Impact factor: 11.025

6.  Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy.

Authors:  Kristien Verhoeven; Peter De Jonghe; Katrien Coen; Nathalie Verpoorten; Michaela Auer-Grumbach; Jennifer M Kwon; David FitzPatrick; Eric Schmedding; Els De Vriendt; An Jacobs; Veerle Van Gerwen; Klaus Wagner; Hans-Peter Hartung; Vincent Timmerman
Journal:  Am J Hum Genet       Date:  2003-01-21       Impact factor: 11.025

Review 7.  Inherited peripheral neuropathies.

Authors:  Mario A Saporta; Michael E Shy
Journal:  Neurol Clin       Date:  2013-03-05       Impact factor: 3.806

Review 8.  Hereditary sensory neuropathy type I.

Authors:  Michaela Auer-Grumbach
Journal:  Orphanet J Rare Dis       Date:  2008-03-18       Impact factor: 4.123

9.  Charcot-Marie-Tooth Type 2B: A New Phenotype Associated with a Novel RAB7A Mutation and Inhibited EGFR Degradation.

Authors:  Paola Saveri; Maria De Luca; Veronica Nisi; Chiara Pisciotta; Roberta Romano; Giuseppe Piscosquito; Mary M Reilly; James M Polke; Tiziana Cavallaro; Gian Maria Fabrizi; Paola Fossa; Elena Cichero; Raffaella Lombardi; Giuseppe Lauria; Stefania Magri; Franco Taroni; Davide Pareyson; Cecilia Bucci
Journal:  Cells       Date:  2020-04-21       Impact factor: 6.600

10.  Factors Affecting Phenotype Variability in a Family with CMT2B: Gender and LRSAM1 Genotype.

Authors:  Leema Reddy Peddareddygari; Kinsi Oberoi; Jaasrini Reddy Vellore; Raji P Grewal
Journal:  Case Rep Neurol       Date:  2016-06-06
  10 in total

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