Neurofibromatosis Syndrome Type II
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Neurofibromatosis type 2 : The Lancet
thelancet.com — “Neurofibromatosis type 2. By - Dr Ashok R Asthagiri MD, Dilys M Parry PhD, John A Butman MD, H Jeffrey Kim MD, Ekaterini T Tsilou MD, Prof Zhengping Zhuang MD, Prof Russell R Lonser MD” View full resource at thelancet.com
Most Recently Shared on June 1, 2009 at 4:22 pm By:
M Auron MD Doctor, Pediatrician, Internist, and Physician
Always necessary review (especially for Med-Peds guys like me) - Neurofibromatosis - http://bit.ly/19X7Tr
Legius Syndrome Often Mistaken for Neurofibromatosis Type 1
profreg.medscape.com — “Legius Syndrome Often Mistaken for Neurofibromatosis Type 1” View full resource at profreg.medscape.com
Most Recently Shared on November 19, 2009 at 2:32 pm By:
Medscape Neurology Neurology and Health Site
Legius Syndrome Often Mistaken for Neurofibromatosis Type 1 http://www.medscape.com/viewarticle/712643
Study Examines Challenges Of Diagnosing Neurofibromatosis Type 1-like Syndrome
medicalnewstoday.com — “An analysis of patients with a syndrome similar to the genetic disorder, neurofibromatosis type 1, indicates that diagnosis may be difficult because of shared clinical findings, such as certain pi” View full resource at medicalnewstoday.com
Most Recently Shared on November 20, 2009 at 12:36 pm By:
MNT Neurology News Neurology and Health News
Study Examines Challenges Of Diagnosing Neurofibromatosis Type 1-like Syndrome: An analysis of patients with a .. http://bit.ly/1B4HL8
Study Examines Challenges of Diagnosing Neurofibromatosis Type 1"like Syndrome
newswise.com — “An analysis of patients with a syndrome similar to the genetic disorder, neurofibromatosis type 1, indicates that diagnosis may be difficult because of shared clinical findings, such as certain pigmentary characteristics, according to a study in the November 18 issue of JAMA.” View full resource at newswise.com
Most Recently Shared on November 17, 2009 at 10:39 pm By:
Study Examines Challenges of Diagnosing Neurofibromatosis Type 1-like Syndrome http://bit.ly/13Oa7g
Legius Syndrome Easily Misdiagnosed as Neurofibromatosis Type 1 : Skin & Allergy News
skinandallergynews.com — “Skin & Allergy News Digital Network is the online destination and multimedia properties of Skin & Allergy News, the independent news publication for the dermatology community. Our breaking news covers all areas of medical dermatology, dermatologic surgery, and aesthetic dermatology. We also provide the news by specialty interest: acne and rosacea, atopic dermatitis and eczema, cutaneous oncology, hair and nails, infectious diseases, pediatric dermatology, psoriasis and rheumatologic disorders, s” View full resource at skinandallergynews.com
Most Recently Shared on October 28, 2010 at 5:49 pm By:
Bob Finn - Medical News Net Health News
#Legius Syndrome Easily Misdiagnosed as #Neurofibromatosis Type 1. By: Bruce Jancin for Skin & Allergy News http://bit.ly/dCzWm4
Caring for the Pregnant Woman With Neurofibromatosis
nursingcenter.com — “-Neurofibromatosis (NF) is one of the most common inherited single-gene disorders in humans, and is expressed as two distinct types: Type I (von Recklinghausen disease) and Type II, which occurs much l” View full resource at nursingcenter.com
Most Recently Shared on January 16, 2010 at 12:34 pm By:
Lisa Morris Bonsall Nurse and Advanced Practice Nurse
New CE ~ Caring for the Pregnant Woman With Neurofibromatosis http://bit.ly/93kr8X
Polyglandular Autoimmune Syndrome, Type II: eMedicine Endocrinology
emedicine.medscape.com — “Overview: Polyglandular autoimmune syndrome type II (PGA-II) is the most common of the immunoendocrinopathy syndromes. It is characterized by the obligatory occurrence of autoimmune Addison's disease in combination with thyroid autoimmune diseases and/or type 1 diabetes mellitus ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 14, 2010 at 3:19 am By:
Susan Scroggins Active Health Library and Health Advocate
Polyglandular autoimmune syndrome type 2 is characterized by Addison's disease plus thyroid autoimmune disease...http://bit.ly/dhsev0
Legius syndrome distinct from neurofibromatosis Type 1 - Related Stories - AAP SmartBrief
smartbrief.com — “Legius syndrome can look like neurofibromatosis Type 1 but is a distinct disorder, and pediatricians and other providers need to recognize the differences, according to researchers from the University of Alabama. They said Legius syndrome, caused by mutations in the SPRED1 gene, is characterized by” View full resource at smartbrief.com
Most Recently Shared on November 20, 2009 at 11:15 pm By:
Clara Song Pediatrician, Physician, and Doctor
Legius syndrome distinct from neurofibromatosis Type 1 http://sbne.ws/r/3jM5
Mucopolysaccharidosis Type II: eMedicine Pediatrics: Genetics and Metabolic Disease
emedicine.medscape.com — “Overview: Hunter syndrome, or mucopolysaccharidosis type II (MPS II), is a member of a group of inherited metabolic disorders collectively termed mucopolysaccharidoses (MPSs). The MPSs are caused by a deficiency of lysosomal enzymes required for the degradation ...” View full resource at emedicine.medscape.com
Most Recently Shared on July 15, 2009 at 9:36 pm By:
Medscape Pediatrics Health Site and Pediatrics
Mucopolysaccharidosis Type II article over at eMedicine has been updated. http://bit.ly/VTYYW #genetics #pediatrics #health #medicine
Polyglandular Autoimmune Syndrome, Type I: eMedicine Endocrinology
emedicine.medscape.com — “Overview: Polyglandular autoimmune (PGA) syndromes (otherwise known as polyglandular failure syndromes) are constellations of multiple endocrine gland insufficiencies. Other descriptive terminologies, such as autoimmune polyendocrine syndrome (APS), also are used in the literature. In the classification of ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 14, 2010 at 3:14 am By:
Susan Scroggins Active Health Library and Health Advocate
Type 1 polyglandular autoimmune syndrome is associated with candidiasis, hypoparathyroidism, and adrenal failure. http://bit.ly/XGXEd
Autoimmune polyglandular syndrome type 2 shows the same HLA class II pattern as type 1 diabetes† - Weinstock - 2011 - Tissue Antigens - Wiley Online Library
onlinelibrary.wiley.com — “Autoimmune polyglandular syndrome type 2 shows the same HLA class II pattern as type 1 diabetes† - Weinstock - 2011 - Tissue Antigens - Wiley Online Library” View full resource at onlinelibrary.wiley.com
Most Recently Shared on March 10, 2011 at 3:23 am By:
Autoimmune polyglandular syndrome type 2 shows the same HLA class II pattern as type 1 diabetes†: In conclusio... http://bit.ly/eKO4ii
Clinical Cases and Images: CasesBlog: John F. Kennedy had the most complex medical history of any U.S. president, likely had polyendocrine syndrome type II
casesblog.blogspot.com — “Health News Updated Daily by an Assistant Professor at University of Chicago, Internist and Allergist” View full resource at casesblog.blogspot.com
Most Recently Shared on September 2, 2009 at 10:50 am By:
Richard L.Trader,Sr Health Executive, Physician Assistant, and Therapist
John F. Kennedy had the most complex medical history of any U.S. president, likely had polyendocrine syndrome ty.. http://bit.ly/RulHd
Complex Regional Pain Syndromes: eMedicine Neurology
emedicine.medscape.com — “Overview: In 1994, a consensus group of pain medicine experts gathered by the International Association for the Study of Pain (IASP) agreed on diagnostic criteria for reflex sympathetic dystrophy (RSD) and causalgia, and renamed them complex regional ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 21, 2010 at 8:59 pm By:
Medscape Neurology Neurology and Health Site
Complex Regional Pain Syndromes: http://bit.ly/c8R2J9
BMC Medical Genetics | Abstract | Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a case report and review o
biomedcentral.com — “Pierre-Robin sequence (PRS) is defined by micro- and/or retrognathia, glossoptosis and cleft soft palate, either caused by deformational defect or part of a malformation syndrome. Neurofibromatosis type 2 (NF2) is an autosomal dominant syndrome caused by mutations in the NF2 gene on chromosome 22q12.2. NF2 is characterized by bilateral vestibular schwannomas, spinal cord schwannomas, meningiomas and ependymomas, and juvenile cataracts. To date, NF2 and PRS have not been described together in the” View full resource at biomedcentral.com
Most Recently Shared on March 22, 2012 at 4:59 am By:
Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child ... http://t.co/1G2H2hVW
Blocked
jama.ama-assn.org — “Blocked” View full resource at jama.ama-assn.org
Most Recently Shared on June 22, 2010 at 9:00 pm By:
Error in a Study of the Clinical and Mutational Spectrum of Neurofibromatosis Type 1-like Syndrome [Letters] http://bit.ly/aL3pjp
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M Auron MD
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Medscape Neurology
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