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Traducción y análisis de palabras por inteligencia artificial ChatGPT
En esta página puede obtener un análisis detallado de una palabra o frase, producido utilizando la mejor tecnología de inteligencia artificial hasta la fecha:
- cómo se usa la palabra
- frecuencia de uso
- se utiliza con más frecuencia en el habla oral o escrita
- opciones de traducción
- ejemplos de uso (varias frases con traducción)
- etimología
Qué (quién) es luxatio imperfecta - definición
SPECIES OF MAMMAL
Didelphis imperfecta; Guianan White-eared Opossum
Amelogenesis imperfecta
DENTAL ENAMEL HYPOPLASIA CHARACTERIZED BY ABNORMAL ENAMEL FORMATION
Amelogenesis Imperfecta; Congenital enamel hypoplasia; Ameleogenesis imperfecta
Amelogenesis imperfecta (AI) is a congenital disorder which presents with a rare abnormal formation of the enamel or external layer of the crown of teeth, unrelated to any systemic or generalized conditions. Enamel is composed mostly of mineral, that is formed and regulated by the proteins in it.
Fernandocrambus imperfecta
SPECIES OF INSECT
Juania imperfecta
Fernandocrambus imperfecta is a moth in the family Crambidae. It was described by John Frederick Gates Clarke in 1965.
brittle bone disease
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![α1 type I collagen]] [[protein]]](https://commons.wikimedia.org/wiki/Special:FilePath/COL1A1 protein - PDB rendering based on 1y0f.jpg?width=200 "α1 type I collagen]] [[protein]]")
![[[Pamidronate]]](https://commons.wikimedia.org/wiki/Special:FilePath/Pamidronate2DACS.svg?width=200 "[[Pamidronate]]")
![[[Preimplantation genetic diagnosis]] is a medical procedure that families with OI can undergo to guarantee non-affected offspring.](https://commons.wikimedia.org/wiki/Special:FilePath/Preimplantation genetic diagnosis.svg?width=200 "[[Preimplantation genetic diagnosis]] is a medical procedure that families with OI can undergo to guarantee non-affected offspring.")
OSTEOCHONDRODYSPLASIA THAT HAS MATERIAL BASIS IN A DEFICIENCY IN TYPE-I COLLAGEN WHICH RESULTS IN BRITTLE BONES AND DEFECTIVE CONNECTIVE TISSUE
Brittle bone disease; Osteogenesis Imperfecta; Ekman-Lobstein disease; Vrolik disease; Brittle Bone Disease; Brittle bones; Cole carpenter syndrome; Lobstein syndrome; Lobstein disease; Bone fragility craniosynostosis proptosis hydrocephalus; Bone fragility with craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features; Van de Hoeve's syndrome; Van der Hoeve's syndrome; Vrolik Syndrome; Vrolik's Syndrome; Osteopetrosis tarda; Osteopsathyrosis; Osteogenisis imperfecta; Fragilitas ossium; OI type I; OI type II; OI type III; OI type IV; OI type 1; OI type 2; OI type 3; OI type 4; OI type IA; OI type I-A; OI type IB; OI type I-B; OI type IVA; OI type IV-A; OI type IVB; OI type IV-B
¦ noun another term for osteogenesis imperfecta or osteoporosis.
Wikipedia
Guianan white-eared opossum
The Guianan white-eared opossum (Didelphis imperfecta) is an opossum species from South America. It is found in Brazil, Suriname, French Guiana and Venezuela.
Possessing the smallest distribution area of its genus, this species is endemic to the Guiana Shield and can inhabit elevations ranging from 80 to 2,250 meters above sea level in the region's lowland forests.
This species, together with the Andean white-eared opossum (D. pernigra), was separated from the white-eared opossum (D. albiventris) in 2002, having been included with that species in 1993.
