RECKLINGHAUSEN'S DISEASE IN А PREGNANT WOMAN: A CLINICAL CASE
Мать и дитя в КузбассеRecklinghausen's disease (neurofibromatosis) was first described in 1882. Neurofibromatosis (non-malignant) is classified as a phacomatosis according to the International Classification of Diseases X revision (Q85.0) and is included in the list of orphan
Владимир Кириллович Чайка +3 more
doaj
Segmental neurofibromatosis: A report of 3 cases
Indian Journal of Dermatology, 2010 Neurofibromatosis is a genetic disorder of neural crest-derived cells that primarily affect growth of neural tissues. It is broadly divided into three categories: (a) von Recklinghausen′s neurofibromatosis or NF-1, (b) bilateral acoustic neuroma ...
Gabhane Sushma +2 more
doaj
The Roots of Neurofibromas in Neurofibromatosis 1 — A Question of Multipotency, Differentiation and Hiding [PDF]
, 2012 Neurofibromatosis type 1 (NF1) is an autosomal dominant cancer predisposition syndrome that affects about 1 in 3500 individuals worldwide. NF1 is caused by mutations in the NF1 gene that encodes the tumor suppressor protein neurofibromin, an ...
Jouhilahti, Eeva-Mari
core +1 more source
The impact of a virtual mind-body program on resilience factors among international English-speaking adults with neurofibromatoses: secondary analysis of a randomized clinical trial. [PDF]
J Neurooncol, 2023 Presciutti AM +7 more
europepmc +1 more source
Neurofibromatose de von Recklinghausen.
Acta Médica Portuguesa, 1989 Neurofibromatosis is a multisystemic disease in which the multiple possible clinical manifestations may have important diagnostic and prognostic implications; if arterial hypertension coexists, many pathogenic mechanisms justify that the possible secondary etiology must be considered.
Ventura, A +4 more
openaire +2 more sources
Neurofibromatosis type 1: natural history and impact on quality of life [PDF]
, 2016 Neurofibromatosis Type 1 (NF1, von Recklinghausen’s disease) is among the more common autosomal dominant genetic disorders, with a worldwide incidence of approximately 1 in 3000 live births. NF1 can occur as either an inherited defect or as a spontaneous
Obagi, Zaidal
core +1 more source
Correction to: Surgical management of peripheral nerve sheath tumours in children, with special consideration of neurofibromatoses. [PDF]
Childs Nerv Syst, 2021 Zipfel J +9 more
europepmc +1 more source
The riddle of multinucleated “floret-like” giant cells and their detection in an extensive gluteal neurofibroma: a case report [PDF]
, 2013 core +1 more source
Orbito-facial plexiform neurofibromatosis: a rare clinical image. [PDF]
Pan Afr Med J, 2023 Sharma A, Daigavane S.
europepmc +1 more source
Evaluating overweight and obesity prevalence in survivors of childhood brain tumors: a systematic review protocol [PDF]
, 2017 core +1 more source