Michael F. Wangler, MD
Department or Service
Assistant Professor, Molecular and Human Genetics
Baylor College of Medicine
|Baylor College of Medicine||fellowship||Molecular & Human Genetics||2011|
|Baylor College of Medicine||residency||Pediatrics||2009|
|Baylor College of Medicine||medical school||Doctor of Medicine||2006|
|Washington University School of Medicine||research fellow||Clinical Research Fellow||2004|
|University of New Mexico School of Medicine||medical school||Medical Student||2003|
The care of children, particularly those with genetic disorders, is a very important privilege that requires training, dedication and a team approach. I feel, as many who trained under him that the late Ralph Feigin gave us a roadmap for what we do at Baylor and Texas Children's in navigating the future of medicine and the challenges we face in the post-genomic era. I am committed to provide the best care for my patients with the most powerful technology and the most current knowledge, but to remain practical and to provide it in a manner that includes compassion and humanity in medical care. Our department also provides a strong mingling of research and clinical care, and the importance of success in research cannot be underestimated with so many genetic disorders that remain untreatable or for which the diagnostic process is not optimal. I am particularly focused on peroxisomal disorders, a rare group of pediatric brain disorders due to a particular defect in body chemistry. I am also actively researching intestinal motility disorders which represent a group of rare, difficult-to-treat diseases.
Tompson SW, Bacino CA, Safina NP, Bober MB, Proud VK, Funari T, Wangler MF, Nevarez L, Ala-Kokko L, Wilcox WR, Eyre DR, Krakow D, Cohn DH. (2010) ?Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene.? American Journal of Human Genetics 87(5): 708-712. PMCID: PMC2978944.