Skeletal Complications in Neurofibromatosis Type 1: The Role of Neurofibromin Haploinsufficiency in Defective Skeletal Remodeling and Bone Healing in NF1

2007 ◽  
Author(s):  
Kevin P. McHugh
Keyword(s):  
Bone Healing ◽  
Neurofibromatosis Type 1 ◽  
Neurofibromatosis Type ◽  
Skeletal Complications

Neurofibromatosis Type 1: The Role of Neuroradiology

1999 ◽  
Vol 30 (03) ◽  
pp. 111-119 ◽  
Author(s):  
W. Mukonoweshuro ◽  
P. Griffiths ◽  
Susan Blaser
Keyword(s):  
Neurofibromatosis Type 1 ◽  
Neurofibromatosis Type

scholarly journals Role of Noncoding RNA ANRIL in Genesis of Plexiform Neurofibromas in Neurofibromatosis Type 1

2011 ◽  
Vol 103 (22) ◽  
pp. 1713-1722 ◽  
Author(s):  
Eric Pasmant ◽  
Audrey Sabbagh ◽  
Julien Masliah-Planchon ◽  
Nicolas Ortonne ◽  
Ingrid Laurendeau ◽  
...  
Keyword(s):  
Neurofibromatosis Type 1 ◽  
Noncoding Rna ◽  
Neurofibromatosis Type ◽  
Plexiform Neurofibromas

Optic gliomas in neurofibromatosis type 1: Role of visual evoked potentials

1994 ◽  
Vol 10 (2) ◽  
pp. 117-123 ◽  
Author(s):  
Kathryn North ◽  
Cheryl Cochineas ◽  
Edward Tang ◽  
Elizabeth Fagan
Keyword(s):  
Evoked Potentials ◽  
Visual Evoked Potentials ◽  
Neurofibromatosis Type 1 ◽  
Neurofibromatosis Type ◽  
Visual Evoked

Neurofibromatosis Type 1 of the head and neck: dilemmas in management

2001 ◽  
Vol 115 (2) ◽  
pp. 151-154 ◽  
Author(s):  
Fernando Rapado ◽  
Ricard Simo ◽  
Mike Small
Keyword(s):  
Head And Neck ◽  
Malignant Transformation ◽  
Neurofibromatosis Type 1 ◽  
Neurofibromatosis Type ◽  
Assessment And Monitoring ◽  
Abnormal Bleeding ◽  
Age Range ◽  
Dominant Condition

Neurofibromatosis type 1 (NF 1) or Von Recklinghausen’s disease is an autosomal dominant condition characterized by multiple skin cafe´-au-lait lesions and multiple neurofibromas. In the head and neck neurofibromas have a predilection to arise in th deep planes of the neck. Surgical management is nearly always required for functional or cosmetic reasons or to exclude the possibility of malignant transformation. We present four cases of neurofibroma of the head and neck and illustrate the difficulties inherent in managing this condition, particularly the age range in which it may occur, the risk of malignant transformation, the possibility of abnormal bleeding and the morbidity that may be associated with the surgical resection. The role of magnetic resonance (MR) scan in the assessment and monitoring of these lesions is highlighted. We also report a unique association of a pharyngeal pouch with NF 1 in a young (25-year-old) patient.

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