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  • Marfan syndrome - Symptoms and causes - Mayo Clinic
    Marfan syndrome is a genetic disorder that causes people to have unusually long arms, legs and fingers Your doctor may want to measure your arm span if he or she thinks you might have the disorder
  • Síndrome de Marfan - Síntomas y causas - Mayo Clinic
    Síndrome de Marfan Descripción general El síndrome de Marfan es un trastorno hereditario que afecta el tejido conectivo, es decir, las fibras que sostienen y sujetan los órganos y otras estructuras del cuerpo El síndrome de Marfan afecta más frecuentemente el corazón, los ojos, los vasos sanguíneos y el esqueleto
  • Ehlers-Danlos syndrome - Symptoms and causes - Mayo Clinic
    Overview Ehlers-Danlos syndrome (EDS) is a group of inherited conditions that affect the body's connective tissues These tissues provide support and give flexibility to the skin, joints, blood vessels and organs There are 13 types of Ehlers-Danlos syndrome The most common types cause very flexible joints, fragile skin, and a higher risk of bruising and injury Symptoms typically can be managed
  • Marfan syndrome - Diagnosis and treatment - Mayo Clinic
    Diagnosis Marfan syndrome can be challenging for doctors to diagnose because many connective tissue disorders have similar signs and symptoms Even among members of the same family, the signs and symptoms of Marfan syndrome vary widely — both in their features and in their severity
  • Thoracic aortic aneurysm - Symptoms and causes - Mayo Clinic
    A genetic condition called Marfan syndrome can weaken the wall of the aorta If you have Marfan syndrome or a related condition, such as Loeys-Dietz syndrome or vascular Ehlers-Danlos syndrome, you have a much higher risk of a thoracic aortic aneurysm These conditions also make you more likely to have an aortic rupture or aortic dissection
  • Síndrome de Marfan - Diagnóstico y tratamiento - Mayo Clinic
    Diagnóstico Para los médicos, puede ser difícil diagnosticar el síndrome de Marfan, ya que muchos trastornos del tejido conjuntivo presentan signos y síntomas similares Incluso entre los miembros de la misma familia, los signos y síntomas del síndrome de Marfan varían ampliamente, tanto en lo que respecta a las características como en lo que respecta a la gravedad
  • Marfan syndrome - Doctors and departments - Mayo Clinic
    Marfan syndrome Departments and specialties Mayo Clinic has one of the largest and most experienced practices in the United States, with campuses in Arizona, Florida and Minnesota Staff skilled in dozens of specialties work together to ensure quality care and successful recovery
  • Thoracic aortic aneurysm - Diagnosis and treatment - Mayo Clinic
    Surgery may be recommended for smaller aneurysms if you have a family history of aortic dissection or a condition linked to aortic aneurysm, such as Marfan syndrome The type of surgery done depends on: The cause of the aneurysm Your overall health The location of the aneurysm Types of surgeries and procedures for thoracic aortic aneurysms
  • Marfan Syndrome and Thoracic Aorta Clinic Overview
    The Marfan Syndrome and Thoracic Aorta Clinic is staffed by a multidisciplinary team of doctors trained in heart conditions (cardiologists), heart and blood vessel surgery (cardiovascular surgeons), cardiac imaging, hereditary conditions (medical geneticists), eye conditions (ophthalmologists) and bone and muscle surgery (orthopedic surgeons)
  • Marfan syndrome and related disorders - Mayo Clinic
    The past 30 years have seen much progress in the diagnosis and treatment of Marfan syndrome and related disorders When Victor A McKusick, M D , first described Marfan syndrome in 1955, he predicted that these patients with serious ocular, musculoskeletal and cardiovascular problems would eventually be found to have a mutation in a structural connective tissue protein





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