Henry serves as Chair of the Sudden Cardiac Arrest Foundation Board of Directors. All four of his resuscitators- Alan, Rodney, David, and Bill plan to attend, as well as his children, Catherine, Joseph, and Sarah, and their spouses and fiancé. Risa and Henry are arranging a twentieth re-birthday celebration in May, 2020. He lives with his wife, Risa, a dermatologist, in Baltimore. Henry joined an extremely small group of people in 2004, those survivors of sudden cardiac arrest who have subsequently completed an Ironman triathlon, when he finished Ironman USA in Lake Placid. He testified in 2006 in the Maryland Senate for a bill mandating AEDs in all high schools in the state, and was thrilled that the bill passed. Henry relishes in his full recovery from his cardiac arrest, and like most survivors, is passionate about reducing avoidable deaths from sudden cardiac arrest. After 27 minutes of CPR by four fellow swimmers who were also physicians, he was successfully defibrillated, a striking example of the exception that proves the rule. On May 16th, 2000, at the age of 44, and seven months after completion of the Ironman Triathlon World Championship in Hawaii, Henry had a cardiac arrest in the shower after a swim workout. After completing a glaucoma fellowship in glaucoma at Wilmer, Dr. He completed an internship in internal medicine at Sinai Hospital and his residency in ophthalmology at the Wilmer Eye Institute. He graduated from Harvard University summa cum laude, received his MD from Yale University, and his MHS in health finance and management from the Johns Hopkins Bloomberg School of Public Health. It does not store any personal data.Henry Jampel, MD, is the Odd Fellows Professor of Ophthalmology at the Wilmer Eye Institute of the Johns Hopkins University School of Medicine. The cookie is set by the GDPR Cookie Consent plugin and is used to store whether or not user has consented to the use of cookies. SchwartzJampel syndrome is a rare autosomal recessive disease caused by mutation in the heparan sulfate proteoglycan 2 ( HSPG2) gene. Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia. Localization of the Schwartz-Jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mapping (Nicole et al. Caused by partial loss-of-function mutations in HSPG2 encoding perlecan (Iwata et al. The cookie is used to store the user consent for the cookies in the category "Performance". Genetics of SJS type I (Schwartz-Jampel syndrome) 1. This cookie is set by GDPR Cookie Consent plugin. The cookie is used to store the user consent for the cookies in the category "Other. The cookies is used to store the user consent for the cookies in the category "Necessary". The cookie is set by GDPR cookie consent to record the user consent for the cookies in the category "Functional". The cookie is used to store the user consent for the cookies in the category "Analytics". These cookies ensure basic functionalities and security features of the website, anonymously. Necessary cookies are absolutely essential for the website to function properly.
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