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Ehlers–Danlos syndrome: correlation with headache disorders in a young woman
Ehlers–Danlos syndrome is a rare inherited illness, which includes an autosomal dominant and also a recessive X–linked variant. Its main clinical characteristic is a generalised connective tissue involving collagen and elastin, causing fragile and hyperextensible skin, loose jointedness and bruising...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3452297/ https://www.ncbi.nlm.nih.gov/pubmed/16388346 http://dx.doi.org/10.1007/s10194-005-0256-0 |
Sumario: | Ehlers–Danlos syndrome is a rare inherited illness, which includes an autosomal dominant and also a recessive X–linked variant. Its main clinical characteristic is a generalised connective tissue involving collagen and elastin, causing fragile and hyperextensible skin, loose jointedness and bruising. Many clinical subtypes are described, each of a different severity degree pattern. The correlation of this syndrome and headache disorders is rare. In this paper we describe the case of a young woman with Type II (less severe) Ehlers–Danlos Syndrome and headache. |
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