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Ehlers-Danlos Syndrome, Hypermobility Type: An Underdiagnosed Hereditary Connective Tissue Disorder with Mucocutaneous, Articular, and Systemic Manifestations
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a, b) An 8-year-old girl with Ehlers-Danlos syndrome showing marked... | Download Scientific Diagram
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Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives | Orphanet Journal of Rare Diseases | Full Text
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The role of cutaneous manifestations in the diagnosis of the Ehlers‐Danlos syndromes - Stembridge - 2023 - Skin Health and Disease - Wiley Online Library
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Figure 2 from Ehlers-Danlos Syndrome, Hypermobility Type: An Underdiagnosed Hereditary Connective Tissue Disorder with Mucocutaneous, Articular, and Systemic Manifestations | Semantic Scholar
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Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history - Tinkle - 2017 - American Journal of Medical Genetics Part C: Seminars in
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Ehlers-Danlos Syndrome, Hypermobility Type: An Underdiagnosed Hereditary Connective Tissue Disorder with Mucocutaneous, Articular, and Systemic Manifestations
![The role of cutaneous manifestations in the diagnosis of the Ehlers‐Danlos syndromes - Stembridge - 2023 - Skin Health and Disease - Wiley Online Library The role of cutaneous manifestations in the diagnosis of the Ehlers‐Danlos syndromes - Stembridge - 2023 - Skin Health and Disease - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/669d8460-9bf5-46e5-af82-3d00a016de75/ski2140-fig-0002-m.jpg)
The role of cutaneous manifestations in the diagnosis of the Ehlers‐Danlos syndromes - Stembridge - 2023 - Skin Health and Disease - Wiley Online Library
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