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.

Cough

A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation.


Total: 6

                       


(per page)
PMID (PMCID)
29904455
(5997446)
 OTHER
High Grade Atrioventricular Block in Von Recklinghausen Disease: A Rare Phenomenon.
Lasam G, Lasam M.
Cardiol Res. 2018;9(3):176-179.
A case of a 73-year-old woman with a history of von Recklinghausen disease (neurofibromatosis type 1) who presented initially with a gradual onset of shortness of breath and lightheadedness with no associated fever, chills, angina, palpitations, cough, weight loss, night sweats, nausea, vomiting, or constipation.
29904455
(5997446)
 OTHER
High Grade Atrioventricular Block in Von Recklinghausen Disease: A Rare Phenomenon.
Lasam G, Lasam M.
Cardiol Res. 2018;9(3):176-179.
A case of a 73-year-old woman with a history of von Recklinghausen disease (neurofibromatosis type 1) who presented initially with a gradual onset of shortness of breath and lightheadedness with no associated fever, chills, angina, palpitations, cough, weight loss, night sweats, nausea, vomiting, or constipation.
19688672
 FEMALE Adult
Malignant schwannoma in pregnancy: a case report and literature review.
Kellogg A, Watson WJ.
Am J Perinatol. 2010;27(3):201-4.
A 28-year-old primigravida with known neurofibromatosis type 1 complained of increasing shortness of breath and cough.
18728548
 MALE
Neurofibromatosis type 1 with tracheobronchial neurofibromas: case report with emphasis on tomographic findings.
Irion KL, Gasparetto TD, Marchiori E, Hochhegger B, Rubin AS.
J Thorac Imaging. 2008;23(3):194-6.
A 65-year-old man with neurofibromatosis type 1 (NF-1) presented with a 3-month history of dyspnea and cough.
16048609
 FEMALE
Successful bone marrow transplantation for life threatening xanthogranuloma disseminatum in neurofibromatosis type-1.
Savasan S, Smith L, Scheer C, Dansey R, Abella E.
Pediatr Transplant. 2005;9(4):534-6.
A 2-yr and 9-month-old female patient with neurofibromatosis type-1 presented with hepatomegaly, anemia, thrombocytopenia, and croupy cough and diagnosed with xanthogranuloma disseminatum (XD).
2133177
 MALE Middle Aged
[Lethal pulmonary involvement in neurofibromatosis].
Faintuch JJ, Saito R, Warth Mdo P, Rocha Ados S.
Rev Hosp Clin Fac Med Sao Paulo. 1990;45(5):219-22.
A unusual case of a 61-year-old man who presented dyspnea and cough associated to skin and subcutaneous lesions typical of neurofibromatosis type 1 is reported.