Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

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.

Neck pain

An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the neck.

Total: 1

(per page)

PMID (PMCID)
27299072 (4719405)	OTHER
	Are Two Surgeries Necessary for Correction of 1 Deformity- Cervical Kyphosis in Neurofibromatosis?- A Rare Case Report.
	Choksey KR, Modi JV. J Orthop Case Rep. 2015;5(3):60-2.
	A 13-year-old boy, a case of neurofibromatosis type 1 presented with neck pain, and bilateral upper limb radiculopathy for 2 months with affected daily living, with intact neurology.