Common recessive limb girdle muscular dystrophies differential diagnosis: why and how?
Limb girdle muscular dystrophies are heterogeneous autosomal hereditary neuromuscular disorders. They produce dystrophic changes on muscle biopsy and they are associated with mutations in several genes involved in muscular structure and function. Detailed clinical, laboratorial, imaging, diagnostic...
Saved in:
| Main Authors: | Ana Cotta, Elmano Carvalho, Antonio Lopes da-Cunha-Júnior, Júlia Filardi Paim, Monica M. Navarro, Jaquelin Valicek, Miriam Melo Menezes, Simone Vilela Nunes, Rafael Xavier Neto, Reinaldo Issao Takata, Antonio Pedro Vargas |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Thieme Revinter Publicações
2014-09-01
|
| Series: | Arquivos de Neuro-Psiquiatria |
| Subjects: | |
| Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2014000900721&lng=en&tlng=en |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Duplicação entérica cística
by: Anna Carolina Pereira Staico, et al.
Published: (2024-03-01) -
Single-centre experience with autosomal recessive limb-girdle muscular dystrophy: case series and literature review
by: Paulo José Lorenzoni, et al.
Published: (2023-10-01) -
Merosin-positive congenital muscular dystrophy: neuroimaging findings Distrofia muscular congênita merosina-positiva: achados de neuroimagem
by: André Palma da Cunha Matta, et al.
Published: (2007-03-01) -
Diagnóstico de linfangioma cavernoso de face em paciente adulto: relato de caso clínico
by: Edela Puricelli, et al.
Published: (2021-07-01) -
Autosomal recessive spastic ataxia of Charlevoix-Saguenay: a family report from South Brazil
by: Daniela Burguêz, et al.