Summary

for people ages up to 80 years (full criteria)
healthy people welcome
at UC Davis
study started
estimated completion:

Description

Summary

Craniosynostosis (CS) is a common malformation occurring in ~4 per 10,000 live births in which the sutures between skull bones close too early, causing long-term problems with brain and skull growth. Infants with CS typically require extensive surgical treatment and may experience many perioperative complications, including hemorrhage and re-synostosis. Even with successful surgery, children can experience developmental and learning disabilities or vision problems. Most often, CS appears as isolated nonsyndromic CS (NSC). Of the several subtypes of CS, unilateral or bilateral fusion of the coronal suture is the second most common form of CS accounting for 20-30% of all NSC cases. The etiology of coronal NSC (cNSC) is not well understood, although the published literature suggests that it is a multifactorial condition. About 5-14% of coronal craniosynostosis patients have a positive family history, with a specific genetic etiology identified in >25% of cNSC cases, suggesting a strong genetic component in the pathogenesis of this birth defect. The causes for cNSC and its phenotypic heterogeneity remain largely unknown. An international team of investigators will generate large genomic and gene expression datasets on samples from patients with cNSC. State-of-the-art imaging, genetic, and developmental and systems biology approaches will be used to quantitatively model novel pathways and networks involved in the development of cNSC. Novel variant-, gene- and network-level analyses will be performed on the genomic data obtained from cNSC cases, their relatives, and controls to identify novel variants and genetic regions associated with cNCS. Quantitative, analytical, and functional validations of these predictions will provide insights into the etiology and possible therapeutic targets for CS and potentially other bone-related disorders.

Official Title

Craniosynostosis Network

Details

The long-term goal of the Program Project, Craniosynostosis Network, is to elucidate normal and abnormal craniofacial biology to ultimately improve the treatment of craniofacial disorders. Craniosynostosis and other skull abnormalities are among the most common human malformations usually requiring surgical and medical intervention. The Network will integrate three projects and two cores. Scientists with diverse expertise including anthropology, morphometry, imaging, birth defects, developmental biology, genetics, genomics, epidemiology, statistics, and systems biology will explore the determinants of the fate of the relevant mesenchymal progenitor cells, abnormalities in osteogenesis that contribute to global skull growth abnormality and premature closure of cranial sutures, especially the coronal suture. High quality genomic data will be obtained from patients with coronal nonsyndromic craniosynostosis (cNSC) and their available parents. Novel genome-wide variant-, gene- and network-level analyses will be performed on these families to identify novel variants and genetic regions associated with coronal craniosynostosis.

This study is a multi-center, open-enrollment, retrospective study, employing both family-based and case-control study designs.

Approximately 4000 cNSC patients, their family members, and controls will be recruited by Mount Sinai and the majority will be recruited from the more than 10 collaborating institutions worldwide.

Keywords

Craniosynostosis Bone Birth Defect Congenital Anomaly Malformation Genetics Genomics Skull Human Mouse Imaging Cell Biology Induced Pluripotent Stem Cells System Biology Craniosynostoses Craniosynostosis Network Environmental Survey 2D/3D Photography Buccal Swab Cell Sampling Blood sampling Skin Biopsy Tissues from a Clinically Indicated Procedure Pre-operative CT Scan Image Files. Coronal Nonsyndromic Craniosynostosis, trios Coronal, nonsyndromic craniosynostosis

Eligibility

You can join if…

Open to people ages up to 80 years

  • Cases with diagnosis of coronal
  • Unaffected relatives of cases
  • Unaffected controls including those who may have undergone clinically indicated craniofacial surgery for trauma or conditions other than craniosynostosis or bone disease. These individuals will be recruited at some of the other collaborating institutions, but not at Mount Sinai.

Individuals of any racial or ethnic group with the established or suspected clinical diagnosis of coronal, nonsyndromic craniosynostosis will be included in this study.Unaffected relatives, such as their biological parents and/or sibs, will also be included to contribute medical information and samples as negative controls for our study.

You CAN'T join if...

  • Those who fit the criteria, but who choose not to participate
  • Those who do not meet the criteria.
  • Other than children, no vulnerable individuals will be recruited, such as intellectual impaired individuals or prisoners.

Locations

  • The International Craniosynostosis Consortium at University of California at Davis accepting new patients
    Davis California 95616 United States
  • Univ. of Texas at Southwestern accepting new patients
    Dallas Texas 75390 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Icahn School of Medicine at Mount Sinai
Links
Information about craniosynostosis and the Craniosynostosis Network Project
ID
NCT03025763
Study Type
Observational
Last Updated