Neurofibromatosis type I: points to be considered by general pediatricians
Neurofibromatosis type 1 (NF1), a prevalent genetic disease that is transmitted in an autosomal dominant manner, is characterized by multiple cutaneous café-au-lait spots and neurofibromas as well as various degrees of neurological, skeletal, and neoplastic manifestations. The clinical features of N...
Main Authors: | Eungu Kang, Hee Mang Yoon, Beom Hee Lee |
---|---|
Format: | Article |
Language: | English |
Published: |
The Korean Pediatric Society
2021-04-01
|
Series: | Clinical and Experimental Pediatrics |
Subjects: | |
Online Access: | http://www.e-cep.org/upload/pdf/cep-2020-00871.pdf |
Similar Items
-
Caracterización clínica de pacientes con neurofibromatosis segmentaria Clinical characterization of patients with segmental neurofibromatosis
by: Miladys Orraca Castillo, et al.
Published: (2012-04-01) -
Spinal neurofibromatosis with NF1 mutation in a classic neurofibromatosis type 1 family: A case report and literature review
by: Zeqian Ning, et al.
Published: (2020-01-01) -
Cariotipo de alta resolución en sangre periférica en la Neurofibromatosis 1 High Resolution Karyotype in Peripheral Blood in Neurofibromatosis 1
by: Miladys Orraca Castillo, et al.
Published: (2009-06-01) -
Prevalence of Associated Endocrine Diseases in Patients with Neurofibromatosis Type 1
by: Aysha Alshahrani, et al.
Published: (2022-01-01) -
Molecular Diagnosis of Neurofibromatosis by Multigene Panel Testing
by: Zeng-Yun-Ou Zhang, et al.
Published: (2021-03-01)