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.

Vitiligo

Total: 2

(per page)

PMID (PMCID)
18577055	MIXED_SAMPLE	Child
	Autoimmune diseases associated with neurofibromatosis type 1.
	Nanda A. Pediatr Dermatol. 2008;25(3):392-3.
	The associations of neurofibromatosis type 1 with vitiligo, alopecia areata, and autoimmune thyroiditis have not been reported earlier.
18577055	MIXED_SAMPLE	Child
	Autoimmune diseases associated with neurofibromatosis type 1.
	Nanda A. Pediatr Dermatol. 2008;25(3):392-3.
	In the present report, we describe two patients of neurofibromatosis type 1 having an association with vitiligo in one, and alopecia areata and autoimmune thyroiditis in another.