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1.
Am J Med Genet C Semin Med Genet ; 175(1): 195-211, 2017 03.
Artículo en Inglés | MEDLINE | ID: mdl-28220607

RESUMEN

The Ehlers-Danlos syndromes (EDS) are a heterogeneous group of heritable connective tissue disorders characterized by joint hypermobility, skin extensibility, and tissue fragility. This communication briefly reports upon the neurological manifestations that arise including the weakness of the ligaments of the craniocervical junction and spine, early disc degeneration, and the weakness of the epineurium and perineurium surrounding peripheral nerves. Entrapment, deformation, and biophysical deformative stresses exerted upon the nervous system may alter gene expression, neuronal function and phenotypic expression. This report also discusses increased prevalence of migraine, idiopathic intracranial hypertension, Tarlov cysts, tethered cord syndrome, and dystonia, where associations with EDS have been anecdotally reported, but where epidemiological evidence is not yet available. Chiari Malformation Type I (CMI) has been reported to be a comorbid condition to EDS, and may be complicated by craniocervical instability or basilar invagination. Motor delay, headache, and quadriparesis have been attributed to ligamentous laxity and instability at the atlanto-occipital and atlantoaxial joints, which may complicate all forms of EDS. Discopathy and early degenerative spondylotic disease manifest by spinal segmental instability and kyphosis, rendering EDS patients prone to mechanical pain, and myelopathy. Musculoskeletal pain starts early, is chronic and debilitating, and the neuromuscular disease of EDS manifests symptomatically with weakness, myalgia, easy fatigability, limited walking, reduction of vibration sense, and mild impairment of mobility and daily activities. Consensus criteria and clinical practice guidelines, based upon stronger epidemiological and pathophysiological evidence, are needed to refine diagnosis and treatment of the various neurological and spinal manifestations of EDS. © 2017 Wiley Periodicals, Inc.


Asunto(s)
Síndrome de Ehlers-Danlos/patología , Enfermedades del Sistema Nervioso/patología , Enfermedades de la Columna Vertebral/patología , Comorbilidad , Síndrome de Ehlers-Danlos/complicaciones , Síndrome de Ehlers-Danlos/fisiopatología , Humanos , Dolor Musculoesquelético/etiología , Enfermedades del Sistema Nervioso/diagnóstico , Guías de Práctica Clínica como Asunto , Enfermedades de la Columna Vertebral/diagnóstico
2.
Fam Community Health ; 33(4): 318-28, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-20736758

RESUMEN

While breast-feeding initiation and duration among US Latina women appear to decrease with acculturation, health care providers in the Greater Cincinnati area have noted lower rates of breast-feeding among even first-generation Latina immigrants. This study's purpose was to identify determinants of breast-feeding for Latina mothers in Cincinnati through qualitative interviews and Spanish Breastfeeding Self-Efficacy Scale ratings. Our findings suggest that, along with similar levels of breast-feeding self-confidence, foreign-born Latina women in the Greater Cincinnati area share similar breast-feeding determinants with the general population. However, characteristics of these determinants and their impact vary because of unique pressures experienced by this community.


Asunto(s)
Lactancia Materna/psicología , Hispánicos o Latinos/psicología , Adulto , Lactancia Materna/estadística & datos numéricos , Cultura , Femenino , Humanos , Modelos Psicológicos , Madres , Ohio , Autoeficacia , Esposos , Adulto Joven
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