Genomic Study of Disorders of Unknown Causes

Genomic Study of Disorders of Unknown Causes

Es posible que algunos contenidos no estén disponibles en español.

Purpose of this Study

If you and your family join this study, you will:
  • Have a 2-3 hour visit in the clinic to meet with the study doctor
  • Have blood drawn for a test called Exome sequencing
  • Have a telephone discussion of test results when they are available (6-9 months after the blood is drawn)
  • Have a 1 hour discussion of test results in the clinic after the telephone discussion

Who Can Participate?

Eligibility

Children and adults who:
  • Have developmental, and/or physical differences that do not have a known cause
  • Have one or both parents to have their blood drawn
  • Have at least one parent who can speak and write in English
  • Have NOT had previous testing called "Exome Sequencing", "Whole Exome sequencing" or "Whole Genome sequencing"

What is Involved?

Description

We are doing this study to better understand the genetic causes of developmental and/or physical differences.

Study Details

Full Title

Genomic Study of Medical, Developmental, or Congenital Problems of Unknown Etiology

Principal Investigator

Vandana
Shashi

Protocol Number

PRO00032301

Phase

N/A

Enrollment Status

Open to Enrollment