Hepatosplenomegaly
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A case of hepatosplenomegaly &lympadenopathy Ppt Powerpoint Presentation slides khaled Medical Slideshow Approach To A Child With Hepatosplenomegaly
slideworld.org — “Powerpoint A case of hepatosplenomegaly &lympadenopathy Slides by khaled Approach To A Child With Hepatosplenomegaly Download Free Medical Powerpoint Presentations” View full resource at slideworld.org
Most Recently Shared on November 17, 2009 at 7:38 am By:
Medical Templates Health Organization
A case of hepatosplenomegaly &lympadenopathy: PowerPoint Presentation on A case of hepatosplenomegaly &lympaden.. http://bit.ly/2APvA5
Lipodystrophy, Generalized: eMedicine Dermatology
emedicine.medscape.com — “Overview: Generalized lipodystrophy syndrome is the association of acanthosis nigricans (AN) with the generalized complete absence of subcutaneous fat and the presence of muscle hypertrophy, hyperlipemia, diabetes mellitus, and hepatosplenomegaly with cirrhosis. Two forms of this syndrome ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 10:20 pm By:
Susan Scroggins Health Advocate and Active Health Library
Generalized lipodystrophy (or Beradinelli-Seip syndrome) is a rare genetic skin condition. Learn more about it. http://bit.ly/bUAydR
Lymphohistiocytosis (Hemophagocytic Lymphohistiocytosis): eMedicine Pediatrics: General Medicine
emedicine.medscape.com — “Overview: Hemophagocytic lymphohistiocytosis (HLH) is a rare but potentially fatal disease of normal but overactive histiocytes and lymphocytes that commonly appears in infancy, although it has been seen in all age groups. Fever, hepatosplenomegaly, pancytopenia, lymphadenopathy, and ...” View full resource at emedicine.medscape.com
Most Recently Shared on July 24, 2009 at 4:54 pm By:
Medscape Pediatrics Pediatrics and Health Site
Another topic with some changes this year, Lymphohistiocytosis, is up at eMedicine.com. http://bit.ly/ylkNQ #medicine #health #pediatrics
Omenn Syndrome: eMedicine Pediatrics: General Medicine
emedicine.medscape.com — “Overview: Omenn syndrome (MIM 603554) is an autosomal recessive form of severe combined immunodeficiency (SCID) characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly. Patients develop fungal, bacterial, and viral infections typical of ...” View full resource at emedicine.medscape.com
Most Recently Shared on July 9, 2010 at 9:49 pm By:
Omenn Syndrome: http://bit.ly/bEkdDL
Griscelli Syndrome: eMedicine Dermatology
emedicine.medscape.com — “Overview: Griscelli and Prunieras1 initially described Griscelli syndrome, or partial albinism with immunodeficiency, in 1978. Griscelli worked at Hospital Necker-Enfants Malades in Paris, France. Griscelli syndrome is a rare autosomal recessive disorder that results in pigmentary ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 18, 2010 at 7:42 pm By:
Julie Bohlen Health Executive and Active Health Library
Griscelli syndrome is a rare genetic disorder that causes pigment issues and lung infections which may be deadly. http://bit.ly/caCTwo
Rheumatology Article | Juvenile rheumatoid arthritis
mdlinx.com — “Recurrent fever of unknown origin (FUO): Aseptic meningitis, hepatosplenomegaly, pericarditis and a double quotidian fever due to juvenile rheumatoid arthritis (JRA)” View full resource at mdlinx.com
Most Recently Shared on April 13, 2011 at 3:01 am By:
Sandeep Pulim MD Physician, Doctor, and Health Communicator
Recurrent fever of unknown origin (FUO): Aseptic meningitis, hepatosplenomegaly, pericarditis and ... http://bit.ly/eL1WfH #Rheumatology
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Medscape Pediatrics
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