Study Examines Challenges of Diagnosing Neurofibromatosis Type 1"like Syndrome

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Study Examines Challenges of Diagnosing Neurofibromatosis Type 1"like Syndrome

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.

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Tags: Genetic, Disease and Condition

Most Recently Shared on November 17, 2009 at 10:39 pm By:

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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 Health News and Neurology

Study Examines Challenges Of Diagnosing Neurofibromatosis Type 1-like Syndrome: An analysis of patients with a .. http://bit.ly/1B4HL8

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JAMA News Releases - November 17, 2009

pubs.ama-assn.org — “Prevalence of High LDL, or 'Bad' Cholesterol Levels Decreases in U.S.;Treatment With Folic Acid, Vitamin B12 Associated With Increased Risk of Cancer, Death;Study Examines Challenges of Diagnosing Neurofibromatosis Type 1-like Syndrome;Telephone-Delivered Care for Treating Depression After Coronary Artery Bypass Graft Surgery Appears to Improve Outcomes;Hospital Quality Report Cards Do Not Appear to Result in Significant Improvements in Processes of Care” View full resource at pubs.ama-assn.org