埃勒斯-丹洛斯综合征
医学
梅德林
重症监护医学
皮肤病科
生物
生物化学
作者
Nikolaus Kernich,Franziska Peters,Julia Schreml,Oliver Semler,Manuel Koch,Eckhard Schönaü,Michael Huntgeburth,Peer Eysel,Thomas Krieg,Esther von Stebut-Borschitz,Iliana Tantcheva‐Poór
出处
期刊:Dermatology
[S. Karger AG]
日期:2024-12-10
卷期号:: 1-23
摘要
(215 words): Introduction: Ehlers-Danlos syndromes (EDS) represent a group of heritable connective tissue disorders characterised by skin hyperelasticity, joint hypermobility and generalized tissue fragility. Many patients remain undiagnosed years after initial symptoms and an accurate diagnosis is difficult despite all efforts. Currently, Germany lacks a patient registry and a specialised EDS centre.
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