Natural History of Craniofacial Anomalies and Developmental Growth Variants
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 2,400
- 试验地点
- 1
- 主要终点
- Database or registry
研究概览
简要总结
Background:
Some head and facial abnormalities are rare and present at birth. Others are more common, and may not show up until puberty. These conditions have different causes and characteristics. Researchers want to learn more about these conditions by comparing people with face, head, and neck abnormalities to family members and to healthy volunteers without such conditions.
Objectives:
To learn more about abnormal development of the face, head, and neck. To determine their genetic variants.
Eligibility:
People who have not had surgery for facial trauma:
People ages 2 and older with craniofacial abnormalities (may participate offsite)
Unaffected relatives ages 2 and older
Healthy volunteers ages 6 and older
Design:
Participants will be screened with medical history and physical exam focusing on head, face, and neck
Participants may be followed for several years. Visits may require staying near the clinic for a few days.
A visit is required for the following developmental stages, along with follow-up visits:
Age 2-6
Age 6-10
Age 11-17
Age 18 and older
Visits may include:
Medical history
Physical exam
Questionnaires
Oral exam
Blood and urine tests
Cheek swab: a cotton swab will be wiped across the inside of the cheek several times.
Cone beam CT scan (CBCT): x-rays create an image of the head, face, teeth, and neck. Participants will
stand still or sit on a chair for about 20 minutes while the scanner rotates around the head.
Photos of the head and face
Offsite participants will provide:
Copies of medical and dental records
Leftover tissue samples from previous surgery
Blood sample or cheek swab
详细描述
Study Description:
This is a natural history study that will examine craniofacial anomalies that affect the normal development of the facial skeleton, including birth defects and dentofacial developmental abnormalities that express themselves with the growth of the individual. Craniofacial anomalies may be rare and present at birth, such as hemifacial microsomia (1 in every 7500 live births), or common, such as dentofacial deformities including the Habsburg Jaw or mandibular prognathism (1% of the US population) that becomes apparent as a child enters puberty. These are striking disorders as they involve the face and surrounding structures, which is a focal point of self-identity and are intimately tied to quality of life and daily function.
Objectives:
Primary Objective:
To characterize and determine genetic variants of rare and common craniofacial anomalies
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 年龄范围
- 2 Years 至 100 Years（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •INCLUSION CRITERIA:
- •For Subjects:
- •Age > 2 to < 100 with craniofacial anomalies/abnormalities. Affected family member (defined as an individual with a demonstrable relationship, any family relationship no matter how distant, with the above subject in the pedigree) who expresses craniofacial anomalies will be classified as a subject.
- •Able to provide consent, or in the case of minors, have a legally authorized representative to provide consent.
- •For Unaffected Family Members:
- •These family members are defined as individuals with a demonstrable relationship (any family relationship, no matter how distant) with a proband subject by pedigree who do not express craniofacial anomalies.
- •>= 2 years old to <= 100 years old.
- •Able to provide consent, or in the case of minors, have a legally authorized representative to provide consent.
- •For Healthy Volunteers:
- •In good general health.
- •>= 6 years old to < 100 years old.
- •Able to provide consent, or in the case of minors, have a legally authorized representative to provide consent.
- •Absence of a craniofacial congenital anomaly or malocclusion.
- •No family history of a craniofacial syndrome.
排除标准
- •An individual who meets any of the following criteria will be excluded from participation in this study:
- •For All Participants:
- •A history of facial trauma requiring surgical treatment and facial reconstruction.
- •Refusal for both genetic testing and CBCT imaging. Participants must agree to at least one of the two (one or the other is required to participate).
- •For Healthy Volunteers:
- •Female volunteers who are pregnant or nursing.
研究组 & 干预措施
1
hemifacial microsomia
2
mandibular prognathism
结局指标
主要结局
Database or registry
时间窗: 17 years
using both extensive clinical evaluations, 3D cone-beam computed tomography-based geometric morphometric and cephalometric analyses, and surface morphology
次要结局
未报告次要终点