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En esta página puede obtener un análisis detallado de una palabra o frase, producido utilizando la mejor tecnología de inteligencia artificial hasta la fecha:
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otomandibular dysostosis - traducción al árabe
HUMAN DISEASE
First and second branchial arch syndrome; Oral-mandibular-auricular syndrome; Otomandibular dysostosis; Craniofacial microsomia; Lateral facial dysplasia; Hemifacial Microsomia; Moeschler Clarren syndrome; First and second brachial arch syndrome; Moeschler–Clarren syndrome; Moeschler-Clarren syndrome
otomandibular dysostosis
خَلَلُ التَّعَظُّمِ الأُذُنِيِّ الفَكِّيّ
cleidocranial dysostosis
OSTEOCHONDRODYSPLASIA THAT HAS MATERIAL BASIS IN MUTATIONS IN THE RUNX2 GENE WHICH RESULTS IN UNDEVELOPED OR ABSENT LOCATED IN CLAVICLE ALONG WITH DELAYED CLOSING OF FONTANELS IN THE LOCATED IN SKULL
Cleidocranial dysplasia; Cleidocranial; Cleidocranial Dysostosis; Craniocleidodysostosis; Mutational dysostosis
خَلَلُ التَّعَظُّمٍ التَّرْقُوِيٌّ القِحْفِيّ, خَلَلُ التَّعَظُّمِ التَّرْقُوِيِّ القِحْفِيّ
mandibulofacial dysostosis
MEDICAL CONDITION
Mandibulofacial dysostosis; Mandibulofacial Dysostosis; Franceschetti-Klein syndrome; Franceschetti syndrome; Tracher-Collins syndrome; Mandubulofacial dysostosis
سوءُ تَعَظُّمِ الفَكِّ السُّفْلِيِّ و الوَجْه
Wikipedia
Hemifacial microsomia
Hemifacial microsomia (HFM) is a congenital disorder that affects the development of the lower half of the face, most commonly the ears, the mouth and the mandible. It usually occurs on one side of the face, but both sides are sometimes affected. If severe, it may result in difficulties in breathing due to obstruction of the trachea—sometimes even requiring a tracheotomy. With an incidence in the range of 1:3500 to 1:4500, it is the second most common birth defect of the face, after cleft lip and cleft palate.[1] HFM shares many similarities with Treacher Collins syndrome.
