Neurofibromatosis type 1

Neurofibromatosis type 1 (NF1) is a clinically heterogeneous, neurocutaneous genetic disorder characterized by café-au-lait spots, iris Lisch nodules, axillary and inguinal freckling, and multiple neurofibromas.

Facial asymmetry

An abnormal difference between the left and right sides of the face.


Total: 2

                       


(per page)
PMID (PMCID)
28538890
(5429116)
 FEMALE Adult
Florid cemento-osseous dysplasia and peripheral giant cell granuloma in a patient with neurofibromatosis 1.
Sarmento DJS, Carvalho SHG, Araujo JCWP Filho, Carvalho MV, Silveira EJDD.
An Bras Dermatol. 2017;92(2):249-252.
We report a 35-year-old mulatto female patient with neurofibromatosis Type 1 who presented with facial asymmetry.
22698902
 FEMALE Infant
Frey syndrome in neurofibromatosis 1.
Ibrahim LF, Brenner C, McMenamin J, Webb D.
BMJ Case Rep. 2011;2011:.
Examination revealed cutaneous features of neurofibromatosis type 1 (NF1) and mild facial asymmetry.