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Maria Luisa Escolar
Maria Luisa Escolar is a pediatrician, clinical professor, and researcher who specializes in pediatric neurodevelopmental disabilities. She is Founder and Director of the Program for the Study of Neurodevelopment in Rare Disorders at Children’s Hospital of Pittsburgh of the University of Pittsburgh Medical Center. Escolar is nationally and internationally known for her research and clinical care of children with leukodystrophies, lysosomal storage diseases, and other inherited metabolic diseases.
==Biography==
Maria Luisa Escolar earned a medical degree at Escuela Colombiana de Medicina in Bogotá, Colombia in 1986; Master of Science in Human Nutrition at Columbia University College of Physicians and Surgeons, New York, NY in 1988; and continued her training in Child Development and Behavioral Pediatrics at New York Hospital–Cornell Medical Center.
In 2000 Escolar established the Early Childhood Clinic at the Clinical Center for the Study of Development and Learning at the University of North Carolina at Chapel Hill to provide comprehensive care for children affected by Krabbe disease and other lysosomal storage disorders.〔 This program became the Neurodevelopmental Function in Rare Disorders and gradually expanded to include other rare neurodegenerative disorders.〔 In 2011, the program moved to the Children’s Hospital of Pittsburgh of the University of Pittsburgh Medical Center and was renamed the Program for the Study of Neurodevelopment in Rare Disorders.〔
Escolar’s work as a pediatrician specializing in rare neurodevelopmental diseases has become well known through word of mouth and media.〔() 〕 Escolar has developed multidisciplinary approaches to diagnose these diseases and assess disease progression and treatment outcomes. She has contributed to articles on the management of mucopolysaccharidosis type II (Hunter syndrome)〔Muenzer J, Beck M, Eng CM, Escolar ML, Giugliani R, Guffon NH, Harmatz P, Kamin W, Kampmann C, Koseoglu ST, Link B, Martin RA, Molter DW, Muñoz Rojas MV, Ogilvie JW, Parini R, Ramaswami U, Scarpa M, Schwartz IV, Wood RE, Wraith E. Multidisciplinary management of Hunter’s syndrome. Pediatr. 2009 Dec;124(6):e1228-e39. DOI: 10.1542/peds.2008-0999〕 and assessment of neurodevelopment in lysosomal storage diseases and related disorders using standardized and validated tools.〔Martin H, Poe MD, Reinhartsen D, Pretzel RE, Roush J, Rosenberg A, Dusing SC, Escolar ML. Methods for assessing lysosomal storage and related disorders: a multidisciplinary perspective. Acta Paediatr Suppl. 2007 Apr;97(457):69-75. DOI: 10.1111/j.1651-2227.2008.00651.x.〕
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