Letter to the Editor
Familial autosomal-dominant carpal tunnel syndrome presenting in a 5-year-old case
Florian Stögbauer MD,
Corresponding Author
Florian Stögbauer MD
Klinik und Poliklinik für Neurologie, Universität Münster, Albert Schweitzer Str. 33, D-48129 Münster, Germany
Klinik und Poliklinik für Neurologie, Universität Münster, Albert Schweitzer Str. 33, D-48129 Münster, Germany
Search for more papers by this author Peter Young MD,
Peter Young MD
Klinik und Poliklinik für Neurologie, Universität Münster, Albert Schweitzer Str. 33, D-48129 Münster, Germany
Search for more papers by this author Harald Funke MD,
Harald Funke MD
Institut für Arterioskleroseforschung und Institut für Klinische Chemie und Laboratoriumsmedizin, Universität Münster, Münster, Germany
Search for more papers by this author
Florian Stögbauer MD,
Corresponding Author
Florian Stögbauer MD
Klinik und Poliklinik für Neurologie, Universität Münster, Albert Schweitzer Str. 33, D-48129 Münster, Germany
Klinik und Poliklinik für Neurologie, Universität Münster, Albert Schweitzer Str. 33, D-48129 Münster, Germany
Search for more papers by this author Peter Young MD,
Peter Young MD
Klinik und Poliklinik für Neurologie, Universität Münster, Albert Schweitzer Str. 33, D-48129 Münster, Germany
Search for more papers by this author Harald Funke MD,
Harald Funke MD
Institut für Arterioskleroseforschung und Institut für Klinische Chemie und Laboratoriumsmedizin, Universität Münster, Münster, Germany
Search for more papers by this author
First published: 07 December 1998
No abstract is available for this article.
References
- 1
Chance PF,
Alderson MK,
Leppig KA,
Lensch MW,
Matsunami N,
Smith B,
Swanson PD,
Odelberg SJ,
Disteche CM,
Bird TD:
DNA deletion associated with hereditary neuropathy with liability to pressure palsies.
Cell
1993;
72:
143–151.
- 2
Pareyson D,
Scaioli V,
Taroni F,
Botti S,
Lorenzetti D,
Solari A,
Ciano C,
Sghirlanzoni A:
Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2 deletion.
Neurology
1996;
46:
1133–1137.
- 3
Vadasz AG,
Chance PF,
Epstein LG,
Lou J-S:
Familial autosomal-dominant carpal tunnel syndrome presenting in a 5-year-old-case. Report and review of the literature.
Muscle Nerve
1997;
20:
376–378.
- 4
Young P.
Wiebusch H,
Stögbauer F,
Ringelstein EB,
Assmann G,
Funke H:
Four frequently observed polymorphisms in the 3′UTR of the human peripheral myelin protein 22 (PMP22) gene.
Clin Genet
1996;
49:
321–322.
- 5
Young P,
Wiebusch H,
Stögbauer F,
Ringelstein EB,
Assmann G,
Funke H:
A frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies (HNPP).
Neurology
1997;
48:
450–452.
