Histochemistry and morphometry of 
Werdnig-Hoffmann disease

Publication:
Histochemistry and morphometry of Werdnig-Hoffmann disease

dc.contributor.author	Pérula, E. Artacho
dc.contributor.author	Villalobos, R. Roldán
dc.contributor.author	Lernos, R. Vaamonde
dc.date.accessioned	2011-01-27T12:46:03Z
dc.date.available	2011-01-27T12:46:03Z
dc.date.issued	1989
dc.description.abstract	We report a case of the Werdnig-Hoffmann disease in a 4-month-old male infant. The morphological study revealed perimysial fibrosis. variability in the size of muscle fibers, absence of target fibers, few central nuclei and normality in vessels, nerves and neuromuscular junctions. The morphometrical examination showed the existence of normal-sized and atrophic fibers in both fibrillar types. as well as in hypertrophic type 1 fibers. The percentage of fibrillar types and the data obtained from the form factor are normal. Random distribution of type 1 and 11 muscle fibers were observed.	es
dc.format	application/pdf	es
dc.format.extent	6	es
dc.identifier.issn	0213-3911
dc.identifier.uri	http://hdl.handle.net/10201/18073
dc.language	eng	es
dc.publisher	Murcia : F. Hernández	es
dc.rights	info:eu-repo/semantics/openAccess	es
dc.subject	Histochemistry	es
dc.subject	Morphometry	es
dc.subject.other	CDU::6 - Ciencias aplicadas::61 - Medicina	es
dc.title	Histochemistry and morphometry of Werdnig-Hoffmann disease	es
dc.type	info:eu-repo/semantics/article	es
dspace.entity.type	Publication	es