of motor unit action potential-like discharges (Fig. ); they disappeared during sleep. With the needle in the masseter, a spatula test 1 was performed. It was positive, and could be documented by EMG monitoring. This case suggests that NNT should be kept in mind and always be considered in neonates
Psychosocial functioning in the Ehlers-Danlos syndrome
✍ Scribed by Lumley, Mark A. ;Jordan, Margaret ;Rubenstein, Ralph ;Tsipouras, Petros ;Evans, Mark I.
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 465 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
✦ Synopsis
Ehlers-Danlos Syndrome (EDS) is a group of related genetic disorders of connective tissue presenting with joint hypermobility, skin extensibility, and tissue fragility. Although the pathophysiology of EDS is increasingly understood, the psychosocial effects of having EDS have not been examined. We psychologically tested and interviewed 41 adults and 7 children with EDS. Anxiety, depression, anger, and interpersonal concerns were significantly elevated, varying from one-quarter to onethird of patients; over 70% had a history of some mental health care use. Psychological difficulties appear to result from chronic pain and disability, ostracism or avoidance of relationships and social activities, sexual difficulties and reproductive concerns, and frustration with the medical system. Specific types of EDS (e.g., EDS '&pe I) are associated with greater pain and psychological distress. Psychological intervention, prescribed with the recognition that psychiatric features are secondary to EDS, is recommended for some patients.
📜 SIMILAR VOLUMES
## Abstract ## Objective Ehlers–Danlos syndrome (EDS) is a clinically and genetically heterogeneous group of heritable connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility. Muscle involvement is plausible based on recently discovered inter
## Abstract We present two unrelated individuals with complete deficiency of tenascin‐X, resulting in an autosomal recessive form of Ehlers–Danlos syndrome (EDS). Consistent with the original description of tenascin‐X deficiency, these individuals had marked skin hyperextensibility, easy bruising,
## Abstract Structural cardiovascular alterations in the classical and hypermobile forms of Ehlers–Danlos syndrome(EDS) warrant investigation. We have examined a cohort of 38 patients with hypermobile and classical EDSs using two‐dimensional echocardiography. The cohort includes 7 males and 31 fema