Type 1 neurofibromatosis and pheochromocytoma: Focus on hypertension

Type 1 neurofibromatosis and pheochromocytoma: Focus on hypertension

Neurofibromatosis 1 (NF1) or von Recklighausen disease, is an autosomal condition caused by heterozygous mutations of the NF1 gene. This genetic disorder occurs in approximately 1 of every 3,000 live births.

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Bibliographische Detailangaben
Veröffentlicht in:Journal of neurosciences in rural practice 2012-01, Vol.3 (1), p.107-108
1. Verfasser: Rocchietti March, Massimiliano
Format: Artikel
Sprache:eng
Schlagworte:
Care and treatment
Diagnosis
Genetic aspects
Genetic disorders
Hypertension
Letters to the Editor
Neurofibromatosis
Neurology
Pheochromocytoma
Risk factors
Tumors
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Beschreibung
Zusammenfassung:Neurofibromatosis 1 (NF1) or von Recklighausen disease, is an autosomal condition caused by heterozygous mutations of the NF1 gene. This genetic disorder occurs in approximately 1 of every 3,000 live births.
ISSN:0976-3147
0976-3155
DOI:10.4103/0976-3147.91987