77 top medical experts on LIG4 Syndrome across 6 countries and 3 U.S. states, including 3 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- LIG4 Syndrome: LIG4 syndrome is a hereditary disorder associated with impaired DNA double-strand break repair mechanisms and characterized by microcephaly, unusual facial features, growth and developmental delay, skin anomalies, and pancytopenia, which is associated with combined immunodeficiency (CID).
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
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