dysplasia$23529$ - translation to ισπανικά
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dysplasia$23529$ - translation to ισπανικά

TEETH HARD TISSUE DISEASE CHARACTERIZED BY PRESENCE OF NORMAL ENAMEL BUT ATYPICAL DENTIN WITH ABNORMAL PULPAL MORPHOLOGY
Dentinal dysplasia; Dentin dysplasia, radicular; Dentin dysplasia, coronal

dysplasia      
n. displasía, defecto en el desarrollo de un órgano o tejido
hearing impairment         
  • A deaf person using a camera-equipped smartphone to communicate in sign language
  • The sign for "friend" in [[American Sign Language]]
  • alt=a female medical professional is seated in front of a special [[sound-proof]] booth with a glass window, controlling diagnostic test equipment. Inside the booth a middle aged man can be seen wearing headphones and is looking straight ahead of himself, not at the [[audiologist]], and appears to be concentrating on hearing something
  • An in-the-canal hearing aid
  • >700}}
{{col-end}}
  • 275x275px
FORM OF HEARING DISORDER
Hearing disability; Hearing Impairment; Hard-of-hearing; Hard of hearing; Hearing-impaired; Partial loss of hearing; Hearing impaired; Hearing Loss; Impairment of hearing; Profoundly deaf; Hearing disorder; Hereditary deafness; Hereditary hearing disorder; Hereditary hearing loss; Congenital deafness; Noise induced deafness; Hearing damage; Profound hearing loss; Hearing disorders; Hypoacusis; Age Related Hearing Impairment; Anacusis; International Symbol for Deafness; Profound deafness; International symbol for deafness; Perceptive deafness; Hardness of hearing; Temporary deafness; Auditory impairment; Partial deafness; Familial deafness; Hearing disorders and deafness; Hearing problems in children; Hearing impairment; Hearing deficits; Loss of hearing; Hearing problems; LY411575; Syndromic deafness; Late-deafened; Scheibe's dysplasia; Scheibes dysplasia; Scheibe dysplasia; Cochleosaccular dysplasia; Hearing problem; Hearing Damage; Sudden hearing loss; DOHH; Bilateral hearing loss; Hearing disabilities
(n.) = deficiencia auditiva, problemas auditivos
Ex: This article provides sources that will enable readers to find other publications that deal with deafness and hearing impairment.
hearing impaired         
  • A deaf person using a camera-equipped smartphone to communicate in sign language
  • The sign for "friend" in [[American Sign Language]]
  • alt=a female medical professional is seated in front of a special [[sound-proof]] booth with a glass window, controlling diagnostic test equipment. Inside the booth a middle aged man can be seen wearing headphones and is looking straight ahead of himself, not at the [[audiologist]], and appears to be concentrating on hearing something
  • An in-the-canal hearing aid
  • >700}}
{{col-end}}
  • 275x275px
FORM OF HEARING DISORDER
Hearing disability; Hearing Impairment; Hard-of-hearing; Hard of hearing; Hearing-impaired; Partial loss of hearing; Hearing impaired; Hearing Loss; Impairment of hearing; Profoundly deaf; Hearing disorder; Hereditary deafness; Hereditary hearing disorder; Hereditary hearing loss; Congenital deafness; Noise induced deafness; Hearing damage; Profound hearing loss; Hearing disorders; Hypoacusis; Age Related Hearing Impairment; Anacusis; International Symbol for Deafness; Profound deafness; International symbol for deafness; Perceptive deafness; Hardness of hearing; Temporary deafness; Auditory impairment; Partial deafness; Familial deafness; Hearing disorders and deafness; Hearing problems in children; Hearing impairment; Hearing deficits; Loss of hearing; Hearing problems; LY411575; Syndromic deafness; Late-deafened; Scheibe's dysplasia; Scheibes dysplasia; Scheibe dysplasia; Cochleosaccular dysplasia; Hearing problem; Hearing Damage; Sudden hearing loss; DOHH; Bilateral hearing loss; Hearing disabilities
discapacitado de oído

Ορισμός

Hyperchromatism
·noun The condition of having an unusual intensity of color.

Βικιπαίδεια

Dentin dysplasia

Dentin dysplasia (DD) is a rare genetic developmental disorder affecting dentine production of the teeth, commonly exhibiting an autosomal dominant inheritance that causes malformation of the root. It affects both primary and permanent dentitions in approximately 1 in every 100,000 patients. It is characterized by presence of normal enamel but atypical dentin with abnormal pulpal morphology. Witkop in 1972 classified DD into two types which are Type I (DD-1) is the radicular type, and type II (DD-2) is the coronal type. DD-1 has been further divided into 4 different subtypes (DD-1a,1b,1c,1d) based on the radiographic features.