Severe dyspnea in a patient with neurofibromatosis type 1
Neurofibromatosis type 1 (NF1) is a genetic disease in which pulmonary complications are rare, but severe, especially pulmonary hypertension (PH). The mechanisms underlying the onset of PH in patients with NF1 are unclear and might be multifactorial. In particular, the frequent presence of pulmonary...
Main Authors: | P.B. Poble, J.C. Dalphin, B. Degano |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2017-01-01
|
Series: | Respiratory Medicine Case Reports |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2213007117301831 |
Similar Items
-
Seizures in children with neurofibromatosis type 1: is neurofibromatosis type 1 enough?
by: Claudia Santoro, et al.
Published: (2018-03-01) -
Facial Plexiform neurofibromatosis in a patient with neurofibromatosis type1: a case report
by: Iffat Hassan, et al.
Published: (2012-01-01) -
Patient with neurofibromatosis type 1 and supratentorial tumor
by: Isabel González Alemán, et al.
Published: (2012-07-01) -
Neurofibromatosis type 1 - some cranial and spinal manifestations
by: B.J. Sher, et al.
Published: (2004-06-01) -
Mosaic neurofibromatosis type 1 or segmental neurofibromatosis: what is in the name?
by: Kakar Shruti, et al.
Published: (2022-01-01)