Study examines challenges of diagnosing neurofibromatosis type 1-like syndrome
Tuesday, November 17, 2009 - 18:35
in Health & Medicine
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.