Microtia (Q46124): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed an Item |
||||||||||||||
| (7 intermediate revisions by the same user not shown) | |||||||||||||||
| description / pt-br | description / pt-br | ||||||||||||||
Microtia é uma malformação congênita de gravidade variável de orelha externa e da média. Tanto fatores hereditários (evidências de microssomia craniofacial familiar e padrões sugestivos de herança multifatorial) quanto acidentes vasculares estão envolvidos na etiologia da doença. Fatores causais específicos também podem incluir rubéola materna durante o primeiro trimestre da gravidez. A microtia comumente envolve o conduto auditivo externo e a orelha média; portanto, a audição pode ser afetada. A microtia pode se apresentar dentro de um espectro de defeitos do arco branquial (microssomia hemifacial, microssomia craniofacial) ou pode se manifestar como uma malformação independente. A aurícula micrótica consiste em um remanescente desorganizado de cartilagem ligado a uma quantidade variável de lóbulo de tecido mole. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Microtia is a congenital malformation of variable severity of the external and middle ear. Both hereditary factors (evidence for familial craniofacial microsomia and patterns suggestive of multifactorial inheritance) and vascular accidents are involved in the etiology of the disease. Specific causative factors also can include maternal rubella during the first trimester of pregnancy. Microtia commonly involves the external canal and middle ear; hence, hearing can be affected. Microtia may present within a spectrum of branchial arch defects (hemifacial microsomia, craniofacial microsomia) or may manifest as an independent malformation. The microtic auricle consists of a disorganised remnant of cartilage attached to a variable amount of soft tissue lobule. | |||||||||||||||
| Property / Canonical URI | |||||||||||||||
| Property / Canonical URI: https://id.who.int/icd/entity/2005415414 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:LA22.0 | |||||||||||||||
| Property / CURIE: CID11:LA22.0 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-LA22.0 | |||||||||||||||
| Property / Canary Token: dki-india-LA22.0 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Linked ICD 10 | |||||||||||||||
| Property / Linked ICD 10: Q17.2 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 14:30, 13 August 2026
Microtia is a congenital malformation of variable severity of the external and middle ear. Both hereditary factors (evidence for familial craniofacial microsomia and patterns suggestive of multifactorial inheritance) and vascular accidents are involved in the etiology of the disease. Specific causative factors also can include maternal rubella during the first trimester of pregnancy. Microtia commonly involves the external canal and middle ear; hence, hearing can be affected. Microtia may present within a spectrum of branchial arch defects (hemifacial microsomia, craniofacial microsomia) or may manifest as an independent malformation. The microtic auricle consists of a disorganised remnant of cartilage attached to a variable amount of soft tissue lobule.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LA22.0 |
||
| English | Microtia |
Microtia is a congenital malformation of variable severity of the external and middle ear. Both hereditary factors (evidence for familial craniofacial microsomia and patterns suggestive of multifactorial inheritance) and vascular accidents are involved in the etiology of the disease. Specific causative factors also can include maternal rubella during the first trimester of pregnancy. Microtia commonly involves the external canal and middle ear; hence, hearing can be affected. Microtia may present within a spectrum of branchial arch defects (hemifacial microsomia, craniofacial microsomia) or may manifest as an independent malformation. The microtic auricle consists of a disorganised remnant of cartilage attached to a variable amount of soft tissue lobule. |
Statements
CID11:LA22.0
0 references
dki-india-LA22.0
0 references
Concluído
0 references
13 August 2026
0 references
