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Ehlers-Danlos Syndrome Type VIIC: A Mexican Case Report
Ehlers-Danlos syndrome (EDS) is a heterogeneous group of heritable connective tissue disorders whose primary clinical features include soft and extensible skin, articular hypermobility and tissue fragility. EDS type VIIC or ‘human dermatosparaxis’ is an autosomal recessive disease characterized by s...
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| Main Authors: | , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
S. Karger AG
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3362267/ https://ncbi.nlm.nih.gov/pubmed/22787447 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000338277 |
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