Dawn L Earl, ARNP
Genetics, Turner Syndrome, Skeletal Health Program
On staff since March 2005
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Dawn is amazing ! I have seen many doctors with my daughter, and Dawn is my absolute favorite ❤️ She is sincere, kind hearted, dedicated and listens to everything and responds really fast to our questions, after we have gone home. My daughter adores her! And I do too! If your taking your child to Dawn, you’ll know you’re well cared for!
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Dawn Earl has been seeing my son since he was 6 months old- He is now 12 years old. She is always caring and very eager to hear all about my son. We truly value the amount of time she spends with us at our visits. She explains things well and also listens well. We never feel rushed or leave with unanswered questions.
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Dawn is wonderfull,amazing,caring,heartfelt. She has made my sons medical process so much better and easier to through go and I recommend her to anyone!
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Amazing, listens companionate. Helped my son who has NF1 he has seizures, tumor on optic nerve had two aneurysms and no moyamoya. It's good having people who care.
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Dawn is a such a delight. My daughter loves to see her. And Dawn takes an interest of the all of our medical needs. And my daughter says she gives awesome back massages.
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Dawn was a godsend when our daughter was diagnosed. She walked us through the maze of Children's and connected us with the various specialists we needed. She has a wonderful manner and way to comfort your fears while also providing the facts and information we needed.
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My son sees Dawn for a chromosome issue and we love her! She always takes her time with him and genuinely cares. She keeps up to date on him and goes above and beyond the call of her duties. If you have a chance to work with her you will be amazed as well!
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Award Name Award Description Awarded By Award Date Cedars-Sinai Medical Center's President's Award June 1999 Commencement Student Marshal June 1997 Chironian Award June 1997 Graduate Student Nurse Association - President 1996 - 1997 Golden Key National Honor Society - Member -
Other Publications
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Robin NH, Taylor CJ, McDonald-McGinn DM, Zackai EH, Bingham P, Collins KJ, Earl D, Gill D, Granata T, Guerrini R, Katz N, Kimonis V, Lin JP, Lynch DR, Mohammed SN, Massey RF, McDonald M, Rogers RC, Splitt M, Stevens CA, Tischkowitz MD, Stoodley N, Leventer RJ, Pilz DT, Dobyns WBPolymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation.
17036343 American journal of medical genetics. Part A, 2006 Nov. 15 : 140(22)2416-25 -
Graham JM Jr, Kreutzman J, Earl D, Halberg A, Samayoa C, Guo XDeformational brachycephaly in supine-sleeping infants.
15689919 The Journal of pediatrics, 2005 Feb. : 146(2)253-7 -
Graham JM Jr, Gomez M, Halberg A, Earl DL, Kreutzman JT, Cui J, Guo XManagement of deformational plagiocephaly: repositioning versus orthotic therapy.
15689920 The Journal of pediatrics, 2005 Feb. : 146(2)258-62 -
Schweitzer DN, Yano S, Earl DL, Graham JM JrJohnson-McMillin syndrome, a neuroectodermal syndrome with conductive hearing loss and microtia: report of a new case.
12838563 American journal of medical genetics. Part A, 2003 July 30 : 120A(3)400-5
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Presentations Title Event Location Date A case of mold Morquio syndrome type IVA identified with enzyme testing American College of Medical Genetics Annual Meeting Charolotte, NC March 27, 2012 - March 31, 2012 Recurrence of a 1 Mb 9q34.3 subtelomeric deletion in siblings detected by oligonucleotide array American College of Medical Genetics Annual Meeting Albuquerque, NM March 24, 2010 - March 28, 2010 A patient with opsismodysplasia treated with bisphosphonate International Skeletal Dysplasia Society Conference Albi, France July 19, 2007 - July 22, 2007 Larsen syndrome: clinical and radiographic delineation and review of health management recommendations Cedars-Sinai Medical Center Nursing Research and Quality Assurance Conference Los Angeles, CA May 4, 2004 Larsen syndrome: clinical and radiographic delineation Western Society for Pediatric Research Meeting Carmel, CA Jan. 28, 2004 - Jan. 31, 2004 Brachydactyly D with cleft lip and scoliosis, a new broadly variable autosomal dominant syndrome Proceedings of the Greenwood Genetics Center 2003 Management and outcomes in 308 cases of torticollis-plagiocephaly deformation sequence Pediatric Academic Societies Meeting Baltimore, MD May 4, 2002 - May 7, 2002 Microcephalic Osteodysplastic Dysplasia: progression of radiographic manifestations not previously described American Society of Human Genetics Meeting San Diego, CA Oct. 12, 2001 - Oct. 16, 2001 A patient with Boston craniosynostosis XXI David W. Smith Workshop on Malformations and Morphogenesis Lake Arrowhead, CA Sept. 7, 2001 - Sept. 11, 2001 Congenital Midline Cervical Cleft, a rare malformation of branchial arch derivation American Society of Human Genetics Meeting Philadelphia, PA Oct. 3, 2000 - Oct. 7, 2000 Johnson-McMillin syndrome, a new neuroectodermal syndrome with conductive hearing loss and microtia: report of a new case American Society of Human Genetics Meeting Philadelphia, PA Oct. 3, 2000 - Oct. 7, 2000 Marden-Walker syndrome: case report and review Annual Clinical Genetics Meeting Palm Springs, CA March 9, 2000 - March 12, 2000 Vertex birth molding: long term residual effects and suggested management of cone-headed neonates Western Society for Pediatric Research Meeting Carmel, CA Feb. 9, 2000 - Feb. 12, 2000
Overview
- Board Certification(s)
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Nurse Practitioner, Pediatric, Primary Care
Advanced Genetics Nursing
- Medical/Professional School
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University of California Los Angeles, Los Angeles, CA
University of Washington, Seattle, WA - Fellowship
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National Institutes of Health, Bethesda, MD
