Literature DB >> 2646524

Hereditary motor-sensory neuropathies. Charcot-Marie-Tooth syndrome.

T D Bird1.   

Abstract

The Charcot-Marie-Tooth (CMT) syndrome is also referred to as hereditary motor-sensory neuropathy (HMSN). It is not a single disease but has a multitude of genetic causes. The typical clinical characteristics are distal muscle weakness and atrophy, depressed tendon reflexes, often slow motor NCV, and the frequent finding of other similarly affected relatives. The most common variant of this syndrome is HMSN-I showing autosomal dominant inheritance, markedly slow motor NCV and nerve hypertrophy. One form of HMSN-I is linked to the Duffy locus on chromosome 1. There are numerous other varieties of HMSN including other autosomal dominant conditions such as HMSN-II (with nearly normal motor NCV) and several types of familial amyloid neuropathy (with specific amino acid substitutions in transthyretin); autosomal recessive conditions such as HMSN-III (Déjérine-Sottas hypertrophic neuropathy of childhood) and Refsum's disease (defect of phytanic acid metabolism); and conditions produced by mutations on the X chromosome such as X-linked HMSN, Fabry trihexoside storage disease, and adrenomyeloneuropathy. The known biochemical abnormalities, chromosomal locations, clinical findings and genetic counseling of these disorders are reviewed.

Entities:  

Mesh:

Year:  1989        PMID: 2646524

Source DB:  PubMed          Journal:  Neurol Clin        ISSN: 0733-8619            Impact factor:   3.806


  3 in total

1.  Charcot-Marie-Tooth disease: extensive cranial nerve involvement on CT and MR imaging.

Authors:  Todd R Aho; Robert C Wallace; Alan M Pitt; Kumaraswamy Sivakumar
Journal:  AJNR Am J Neuroradiol       Date:  2004-03       Impact factor: 3.825

2.  Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales families.

Authors:  J C MacMillan; M Upadhyaya; P S Harper
Journal:  J Med Genet       Date:  1992-01       Impact factor: 6.318

3.  A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease.

Authors:  Paschalis Nicolaou; Carlo Cianchetti; Anna Minaidou; Giovanni Marrosu; Eleni Zamba-Papanicolaou; Lefkos Middleton; Kyproula Christodoulou
Journal:  Eur J Hum Genet       Date:  2012-07-11       Impact factor: 4.246

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.