File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.ejpn.2005.01.007
- Scopus: eid_2-s2.0-17144380033
- PMID: 15843075
- WOS: WOS:000229054200006
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Peripheral neuropathy - A novel finding in dyskeratosis congenita
Title | Peripheral neuropathy - A novel finding in dyskeratosis congenita |
---|---|
Authors | |
Keywords | Cerebellar ataxia Delayed myelination Dyskeratosis congenita Peripheral neuropathy |
Issue Date | 2005 |
Publisher | WB Saunders Co Ltd. The Journal's web site is located at http://www.elsevier.com/locate/ejpn |
Citation | European Journal Of Paediatric Neurology, 2005, v. 9 n. 2, p. 85-89 How to Cite? |
Abstract | We report the case of a 3.5-year-old boy who presented with truncal ataxia, microcephaly and delayed global development in infancy. Hypoplasia of cerebellum and corpus callosum and delayed myelination were found on brain MRI. Failure to thrive, sparse hairs and dystrophic nails became evident at the age of 2 years. He subsequently developed bleeding tendency, thrombocytopenia and hypocellularity on bone marrow examination leading to a diagnosis of dyskeratosis congenita. Impaired pain perception with slowing of nerve conduction velocities was demonstrated, suggesting a mild peripheral neuropathy. To the best of our knowledge, peripheral neuropathy has never been reported as a feature of the congenital form of dyskeratosis congenita. © 2005 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/170340 |
ISSN | 2023 Impact Factor: 2.3 2023 SCImago Journal Rankings: 0.916 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ip, P | en_US |
dc.contributor.author | Knight, R | en_US |
dc.contributor.author | Dokal, I | en_US |
dc.contributor.author | Manzur, AY | en_US |
dc.contributor.author | Muntoni, F | en_US |
dc.date.accessioned | 2012-10-30T06:07:37Z | - |
dc.date.available | 2012-10-30T06:07:37Z | - |
dc.date.issued | 2005 | en_US |
dc.identifier.citation | European Journal Of Paediatric Neurology, 2005, v. 9 n. 2, p. 85-89 | en_US |
dc.identifier.issn | 1090-3798 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/170340 | - |
dc.description.abstract | We report the case of a 3.5-year-old boy who presented with truncal ataxia, microcephaly and delayed global development in infancy. Hypoplasia of cerebellum and corpus callosum and delayed myelination were found on brain MRI. Failure to thrive, sparse hairs and dystrophic nails became evident at the age of 2 years. He subsequently developed bleeding tendency, thrombocytopenia and hypocellularity on bone marrow examination leading to a diagnosis of dyskeratosis congenita. Impaired pain perception with slowing of nerve conduction velocities was demonstrated, suggesting a mild peripheral neuropathy. To the best of our knowledge, peripheral neuropathy has never been reported as a feature of the congenital form of dyskeratosis congenita. © 2005 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved. | en_US |
dc.language | eng | en_US |
dc.publisher | WB Saunders Co Ltd. The Journal's web site is located at http://www.elsevier.com/locate/ejpn | en_US |
dc.relation.ispartof | European Journal of Paediatric Neurology | en_US |
dc.subject | Cerebellar ataxia | - |
dc.subject | Delayed myelination | - |
dc.subject | Dyskeratosis congenita | - |
dc.subject | Peripheral neuropathy | - |
dc.subject.mesh | Child, Preschool | en_US |
dc.subject.mesh | Demyelinating Diseases - Diagnosis - Etiology - Physiopathology | en_US |
dc.subject.mesh | Dyskeratosis Congenita - Complications | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Neural Conduction - Physiology | en_US |
dc.subject.mesh | Peripheral Nervous System Diseases - Diagnosis - Etiology - Physiopathology | en_US |
dc.title | Peripheral neuropathy - A novel finding in dyskeratosis congenita | en_US |
dc.type | Article | en_US |
dc.identifier.email | Ip, P:patricip@hku.hk | en_US |
dc.identifier.authority | Ip, P=rp01337 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/j.ejpn.2005.01.007 | en_US |
dc.identifier.pmid | 15843075 | - |
dc.identifier.scopus | eid_2-s2.0-17144380033 | en_US |
dc.identifier.hkuros | 98110 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-17144380033&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 9 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.spage | 85 | en_US |
dc.identifier.epage | 89 | en_US |
dc.identifier.isi | WOS:000229054200006 | - |
dc.publisher.place | United Kingdom | en_US |
dc.identifier.scopusauthorid | Ip, P=7003622681 | en_US |
dc.identifier.scopusauthorid | Knight, R=8356641100 | en_US |
dc.identifier.scopusauthorid | Dokal, I=7003881972 | en_US |
dc.identifier.scopusauthorid | Manzur, AY=7004508063 | en_US |
dc.identifier.scopusauthorid | Muntoni, F=7102038246 | en_US |
dc.identifier.issnl | 1090-3798 | - |