Dr. Aneal Khan

MSC, MD, FAAP, FRCPC, FCCMG

Assistant Professor of Medical Genetics and Pediatrics

Alberta Children's Hospital, University of Calgary

3rd Floor Metabolic Clinic

2888 Shaganappi Trail NW

Calgary, Alberta, Canada, T3B 6A8

Tel: (403)-955-7587    Fax: (403)-955-3091

Email: 

 

Research Interests

Jia-Chi Wang and Aneal Khan.  Large distal 5p deletion with hemifacial microsomia and absence of cri-du-chat syndrome.  Clin Dysmorphol 2010 Jan;19(1):38-9.

Khan A. and Potter M. Inborn Errors of Metabolism: Critical Care Perspective. In: Kirpalani H, Huang L, Michenko M. Editors; Manual of Pediatric Intensive Care, BC Decker, 2010.

Khan A, Caluseriu O, Huang LH, Robin NH. Williams Syndrome. eMedicine from WebMD. Updated November 18, 2009. Available at: http://emedicine.medscape.com/article/893149-overview.

Aneal Khan, Barbara Ramage, Ion Robu, and Laura Benard.  Side-Alternating Vibration Training Improves Muscle Performance in a Patient with Late-Onset Pompe Disease.  Case Reports in Medicine. 2009; Article ID 741087, doi:10.1155/2009/741087.

Linda M. Reis, Rebecca Tyler, Joseph Toonen, Omar Abdul-Rahman, Pamela Trapane, Robert Wallerstein, Diane Broome, Jodi Hoffman, Aneal Khan, Christina Paradiso, Nitin Ron, Amanda Bergner,Elena V. Semina. Identification of Novel B3GALTL Mutations and Evidence for Genetic Heterogeneity in Peters-Plus Syndrome. American Journal of Medical Genetics 2008;146:2603–2610.

Aneal Khan, Harvey B. Sarnat, and Renee Spaetgens.  Congenital Muscle Fiber Type Disproportion in a case with Central Congenital Hypoventilation Syndrome due to PHOX2B mutations. J Child Neurol 2008;23(7):829-31.

Aneal Khan, Jacqueline Bourgeois, and Patrick Mohide. Agnathia-Otocephaly Complex in a Fetus with Maternal Use of 1% Topical Salicylate. Clinical Dysmorphology 2008;17:75-6.

Aneal Khan, Josephine Ho, Amy Pender, Xingchang Wei and Murray Potter. I-Cell Disease (Mucolipidosis II) Presenting as Neonatal Fractures: A Case for Continued Monitoring of Serum Parathyroid Hormone Levels.  Clin Pediatr Endocrinol 2008;17(3):81-85.

Wang JC, Dang L, Mondal TK, Khan A. Prenatally diagnosed mosaic trisomy 22 in a fetus with left ventricular non-compaction cardiomyopathy. Am J Med Genet A. Nov 15 2007;143(22):2744-2746.

Khan AA, Hyde RK, Dutra A, Mohide P, Liu P. Core binding factor beta (CBFB) haploinsufficiency due to an interstitial deletion at 16q21q22 resulting in delayed cranial ossification, cleft palate, congenital heart anomalies, and feeding difficulties but favorable outcome.  American Journal of Medical Genetics, 2006 Nov 1;140(21):2349-54.

Research Funding

Alberta Children‚Äôs Hospital Research Foundation.  Vibration therapy in mobility-impaired patients with mitochondrial disease. 2009-2010.