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.

Renovascular hypertension

The presence of hypertension related to stenosis of the renal artery.

Total: 1

(per page)

PMID (PMCID)
23815393	MALE	Child
	Neurofibromas of the bladder in a child with neurofibromatosis type 1 causing chronic renal disease.
	Ylmaz K, Dusunsel R, Dursun I, Coskun A, Erten S, Kucukaydn M, Yel S, Gunduz Z. Ren Fail. 2013;35(7):1005-7.
	Neurofibromatosis type 1 (NF1) is an autosomal-dominant inherited disorder and its prominent feature is the neurofibroma and renal involvement includes renal artery stenosis and renal artery aneurysms causing renovascular hypertension.