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  • Moebius syndrome - Wikipedia
    Möbius syndrome or Moebius syndrome is a rare congenital neurological disorder which is characterized by facial paralysis and the inability to move the eyes from side to side
  • Moebius Syndrome: What It Is, Causes, Symptoms Treatment
    Moebius syndrome is a congenital (present at birth) disease It affects babies’ facial muscles, including their ability to smile or move their eyes, but may cause other symptoms
  • What Is Moebius Syndrome?
    As a very simple explanation, Moebius syndrome is a form of facial paralysis combined with outward, to the side, eye paralysis Individuals with Moebius syndrome typically cannot make facial expressions, such as smiling, frowning, squinting, or blinking
  • Moebius Syndrome - Johns Hopkins Medicine
    Moebius syndrome is a rare congenital (present at birth) condition that results from underdevelopment of the facial nerves that control some of the eye movements and facial expressions
  • Moebius syndrome: clinical features, diagnosis, management and early . . .
    Moebius syndrome (MBS) is a rare disease characterized by unilateral or bilateral nonprogressive congenital facial palsy (VII cranial nerve) with impairments of ocular abduction (VI cranial nerve); it can also be associated with other cranial nerve (CN) palsies, orofacial anomalies and limb defects [1]
  • Moebius syndrome: MedlinePlus Genetics
    Moebius syndrome is a rare neurological condition that primarily affects the muscles that control facial expression and eye movement The signs and symptoms of this condition are present from birth Weakness or paralysis of the facial muscles is one of the most common features of Moebius syndrome
  • Moebius syndrome: The rare condition that makes people unable to smile
    Moebius syndrome is a rare condition that affects several cranial nerves, impairing the muscles that control facial expressions and eye movements
  • Möbius Syndrome - EyeWiki
    Möbius syndrome (otherwise spelled Moebius syndrome) is a rare congenital disorder that is part of the cranial congenital dysinnervation disorders It is characterized by non-progressive unilateral or bilateral paralysis of the facial musculature with preservation of the vertical eye movements


















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