Louanne Hudgins
Academic Appointments
- Professor - Med Center Line, Pediatrics - Medical Genetics
- Member, Child Health Research Institute
- Professor - Med Center Line (By courtesy), Obstetrics & Gynecology
Key Documents
Contact Information
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Clinical Offices
Medical Genetics 730 Welch Road, 2nd Floor Palo Alto, CA 94304 Tel Work (650) 721-5804 Fax (650) 498-4555Practices at Stanford Hospital and Clinics and Lucile Packard Children's Hospital
- Academic Offices
Personal Information Email Tel (650) 498-4937Not for medical emergencies or patient use
Professional Overview
Clinical Focus
- Clinical Genetics
- Perinatal Genetics
Honors and Awards
- Mosbacher Family Distinguished Packard Fellow, Stanford University School of Medicine, Department of Pediatrics (2008-present)
Professional Education
| Board Certification: | Clinical Genetics, American Board of Medical Genetics (1993) |
| Fellowship: | University of Connecticut CT (1990) |
| Residency: | University of Connecticut CT (1987) |
| Medical Education: | University of Kansas Medical KS (1984) |
| Internship: | University of Connecticut-School of Medicine CT (1985) |
Scientific Focus
Current Research Interests
I am interested in prenatal genetic screening and diagnosis.
Publications
- Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay. Am J Med Genet A. 2012; (2): 391-9
- Utilization of available prenatal screening and diagnosis: effects of the California screen program. J Perinatol. 2012
- What is your diagnosis? Trichorhinophalangeal syndrome type I. Cutis. 2012; (2): 56, 73-4
- Ectopia lentis as the presenting and primary feature in Marfan syndrome. Am J Med Genet A. 2011; (11): 2661-8
- Familial cardiac valvulopathy due to filamin A mutation. Am J Med Genet A. 2011; (9): 2236-41
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