Mondini cochlea
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Mondini cochlea deafness deformity (malformation) — Mon·di·ni cochlea, deafness, deformity (malformation) (mon deґne) [C. Mondini, Italian physician, 1729–1803] see under cochlea, deafness, and deformity … Medical dictionary
Mondini dysplasia — Mondini Dysplasia, (Mondini malformation, Mondini defect) is an abnormality in the inner ear that can be the cause of hearing loss. A person with Mondini dysplasia has a cochlea that is incomplete. A normal cochlea has two and a half turns, a… … Wikipedia
Mondini-Dysplasie — Klassifikation nach ICD 10 Q 16.5 Angeborene Fehlbildung des Innenohres, Anomalie: Corti Organ, häutiges Labyrinth … Deutsch Wikipedia
Mondini deformity — a misshapen cochlea with dysplasia or aplasia of the bony and membranous labyrinths, as seen in Mondini deafness. Called also Mondini malformation … Medical dictionary
Mondini deafness — congenital deafness due to dysgenesis of the organ of Corti, with partial aplasia of the bony and membranous labyrinth and a resultant flattened cochlea. See also Mondini deformity, under deformity … Medical dictionary
Hearing impairment — See also: Deaf culture for the social movement.. Deaf and/or hard of hearing Classification and external resources The International Symbol for Deafness … Wikipedia
Dysplasia — Abnormal in form. From the Greek dys (bad, disordered, abnormal) and plassein (to form). For example, retinal dysplasia is abnormal formation of the retina during embryonic development. * * * Abnormal tissue development. SEE ALSO: heteroplasia.… … Medical dictionary
Hörschnecke — Ausguss eines menschlichen Labyrinths Die Hörschnecke (lat. Cochlea) ist ein Teil des Innenohrs und stellt das Rezeptorfeld für die Hörwahrnehmung dar. Inhaltsverzeichnis … Deutsch Wikipedia
hearing impairment, hearing loss — A reduction in the ability to perceive sound; may range from slight inability to complete deafness. SEE ALSO: deafness, threshold shift. acoustic trauma hearing loss sensory hearing … Medical dictionary
Pendred syndrome — Classification and external resources OMIM 274600 DiseasesDB 9771 GeneReviews … Wikipedia
