{Reference Type}: Case Reports
{Title}: A case report of hamartomatous polyposis in an individual with Neurofibromatosis type 1.
{Author}: Boulier K;Erwin DJ;Nagamani S;Eble TN;
{Journal}: Clin Case Rep
{Volume}: 7
{Issue}: 1
{Year}: Jan 2019
暂无{DOI}: 10.1002/ccr3.1908
{Abstract}: Even in well-described genetic syndromes, such as neurofibromatosis type 1, expansion of the phenotype should be considered as a possible explanation for atypical presentations. However, it is critical to complete the evaluation for a potential dual diagnosis, as there could be significant prognostic and management implications.