<--- Back to Details
First PageDocument Content
Hypotension / Syndromes / Dysautonomia / Endocrine diseases / Familial dysautonomia / Orthostatic intolerance / Orthostatic hypotension / Postural orthostatic tachycardia syndrome / Vasovagal response / Health / Anatomy / Medicine
Date: 2013-05-20 02:08:08
Hypotension
Syndromes
Dysautonomia
Endocrine diseases
Familial dysautonomia
Orthostatic intolerance
Orthostatic hypotension
Postural orthostatic tachycardia syndrome
Vasovagal response
Health
Anatomy
Medicine

Your Pediatric Patient is Diagnosed with Dysautonomia.pub

Add to Reading List

Source URL: www.dynainc.org

Download Document from Source Website

File Size: 539,89 KB

Share Document on Facebook

Similar Documents

Rare diseases / Cystic fibrosis transmembrane conductance regulator / Cystic fibrosis / Genotype / Methylenetetrahydrofolate reductase / Warfarin / Pharmacogenetics / Polymorphism / Mutation / Biology / Health / Genetics

Disorder Ashkenazi Jewish Panel: Bloom Syndrome, Canavan Disease, Familial Dysautonomia,

DocID: 18Gmc - View Document

Rare diseases / Cystic fibrosis transmembrane conductance regulator / Cystic fibrosis / Genotype / Methylenetetrahydrofolate reductase / Warfarin / Pharmacogenetics / Polymorphism / Mutation / Biology / Health / Genetics

Disorder Ashkenazi Jewish Panel: Bloom Syndrome, Canavan Disease, Familial Dysautonomia,

DocID: 142Qf - View Document

Genomics / Gastrointestinal cancer / Emerging technologies / Tay–Sachs disease / Personalized medicine / Genetic testing / Familial dysautonomia / GeneDx / Human genome / Medicine / Biology / Genetics

Evaluating the Utility of Genetic Panels

DocID: 13R7z - View Document

Rare diseases / Medical genetics / Lipid storage disorders / Tay–Sachs disease / Genetic disorder / Familial dysautonomia / Recessive / Cystic fibrosis / Genetic testing / Health / Medicine / Genetics

Tay-Sachs Disease and other conditions more common in the Ashkenazi Jewish community Fact Sheet 35 Important points  

DocID: 11ir1 - View Document

Rare diseases / Molecular biology / DNA / Familial dysautonomia / Hypokalemic periodic paralysis / Amyotrophic lateral sclerosis / Gene / Mutation / Hereditary sensory and autonomic neuropathy / Biology / Health / Genetics

Neurogenetics DNA/Biochemical Diagnostic Lab Massachusetts General Hospital Center for Human Genetic Research CRP Building North, Suite[removed]Cambridge Street Boston, MA 02114

DocID: NbyA - View Document