Understanding, Diagnosing, and Using Genetic Testing for Congenital Generalized Lipodystrophy
Congenital generalized lipodystrophy (CGL) is a rare genetic disorder characterized by the near-total absence of adipose tissue from birth.
Brandon Colby, MD
MD · MBA
Physician specializing in genetic analysis and personalized preventive medicine, and author of Outsmart Your Genes.
About Brandon
Brandon Colby is a physician-expert in the fields of genetic analysis and Personalized Preventive Medicine. He holds an MD from the Mount Sinai School of Medicine, an MBA from Stanford University's Graduate School of Business, and a degree in Genetics from the University of Michigan.
Dr. Colby is the author of the book Outsmart Your Genes and has developed numerous technologies that improve the analysis, interpretation, and actionability of genome sequencing data. He is an Affiliate Specialist of the American College of Medical Genetics and Genomics (ACMG), an Associate of the American College of Preventive Medicine (ACPM), and a member of the National Society of Genetic Counselors (NSGC).
Education
- BA in Genetics with Honors, University of Michigan · 2000
- MD, Mount Sinai School of Medicine · 2004
- MBA, Stanford University Graduate School of Business · 2007
Affiliations & Memberships
- Affiliate Specialist, American College of Medical Genetics and Genomics (ACMG)
- Associate, American College of Preventive Medicine (ACPM)
- Member, National Society of Genetic Counselors (NSGC)
Articles by Brandon Colby, MD are reviewed for accuracy by Sequencing's medical and scientific team. This page is for informational purposes and does not constitute medical advice.
Articles by Brandon
Understanding Congenital Heart Disease: Diagnosis and Genetic Testing
Explore congenital heart disease, its diagnosis methods, and the vital role of genetic testing in identifying mutations, assessing risks, and personalizing treatments.
Understanding, Diagnosing, and Using Genetic Testing for Congenital Nystagmus
Unlock the role of genetic testing in diagnosing congenital nystagmus. Identify genetic mutations, personalize treatments, and inform family planning strategies.
Understanding, Diagnosing, and Using Genetic Testing for Congenital Total Pulmonary Venous Return Anomaly
Explore Congenital Total Pulmonary Venous Return Anomaly (TAPVR), its diagnosis, and the impact of genetic testing on early detection and personalized treatment.
Understanding, Diagnosing, and Using Genetic Testing for Craniofacial-Deafness-Hand Syndrome
Explore how genetic testing aids in diagnosing Craniofacial-Deafness-Hand Syndrome. Learn about symptoms, early interventions, and the role of PAX3 gene mutations.
Understanding, Diagnosing, and Using Genetic Testing for Diamond-Blackfan Anemia
Explore Diamond-Blackfan Anemia, including symptoms, diagnosis, and the critical role of genetic testing in identifying ribosomal protein gene mutations for better management.
Understanding, Diagnosing, and Using Genetic Testing for Diffuse Intrinsic Pontine Glioma
Dive into the complexities of Diffuse Intrinsic Pontine Glioma, advanced diagnosis techniques, and the role of genetic testing in creating personalized treatment plans.
Understanding, Diagnosing, and Using Genetic Testing for Duodenal Adenocarcinoma
Duodenal adenocarcinoma is a rare but serious form of cancer that originates in the first section of the small intestine, known as the duodenum.