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Genetic Analysis of PHACE Syndrome (Hemangioma With Other Congenital Anomalies)

Genetic Analysis of PHACE Syndrome.(PHACE Syndrome is Defined as a Hemangioma Plus One or More of the Following: Brain, Heart, Eye, Sternal or Cerebral Artery Anomalies).

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01016756
Acronym
PHACE
Enrollment
341
Registered
2009-11-19
Start date
2007-02-28
Completion date
2022-08-15
Last updated
2023-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

PHACE Syndrome

Keywords

PHACE syndrome, Hemangioma, Coarctation of aorta, Dandy Walker, Brain malformation, Eye anomaly, Sternal malformation, Genetic analysis, Cerebral artery anomaly

Brief summary

1. PHACE syndrome(OMIM database number 606519) is the association of a vascular birthmark (hemangioma) on the face along with one or more of the following conditions: congenital heart defects, congenital anomalies of the cerebral arteries,brain, eyes, or sternum. 2. A research study is currently being conducted at the Medical College of Wisconsin (MCW) to investigate if there is an inherited cause of PHACE syndrome. 3. We are hoping that this study will lead to a better understanding of how and why children develop PHACE syndrome.

Detailed description

If you and your child agree to participate in this study, the following will happen: 1. The principal investigator at MCW, or her appointed representative or collaborators at other sites, will review the study protocol and consent form with you and answer any questions- this can be done over the phone. 2. If you choose to participate, the investigator will obtain informed consent for study participation, consent to obtain medical records, and a small amount of logistical information such as address and phone number. 3. Subjects and parents may have a blood draw, saliva sample or buccal swab done. 4. If the subject undergoes surgery for another reason and there is tissue which would otherwise be discarded, we may ask to receive this sample for research purposes. 5. We will request completion of surveys about the individual's medical history as it relates to this condition. 6. The purpose of this study is to promote the understanding of the inheritance of hemangiomas associated with brain, eye and heart anomalies. The DNA obtained from participants are stored in a DNA repository and genetic data bank for current and future research projects related to their genetic disorders. The DNA specimens will be used to map disease-related genes. The principal investigator uses her discretion to decide which investigators will have access to this resource. The analysis of the specimens will vary depending on the investigator and his/her specific protocol.

Interventions

None listed

Sponsors

Medical College of Wisconsin
Lead SponsorOTHER

Study design

Observational model
FAMILY_BASED
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* meets the clinical diagnostic criteria for PHACE syndrome.

Exclusion criteria

* fails to meet the clinical diagnostic criteria for PHACE syndrome.

Design outcomes

Primary

MeasureTime frame
Establish a DNA and tissue bank.5 years
Determine candidate genes for PHACE syndrome using a genome-wide approach.10 years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026