Cargando…
Neurofibromatosis Type 1 in Children: A Single-Center Experience
OBJECTIVE: Neurofibromatosis (NF) is the most common autosomal dominantly inherited neurocutaneous syndrome. The characteristic features of NF type 1 (NF-1) are café au lait spots, axillary and inguinal freckling, peripheral neurofibromas, optic pathway glioma, and Lisch nodules. The present study a...
Autores principales: | Gonca Kaçar, Ayşe, Kılınc Oktay, Burcu, Çınar Özel, Simge, Ocak, Süheyla, Güneş, Nilay, Uludağ Alkaya, Dilek, Tüysüz, Beyhan, Apak, Hilmi, Tiraje Celkan, Tülin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Turkish Pediatrics Association
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8655961/ https://www.ncbi.nlm.nih.gov/pubmed/35005728 http://dx.doi.org/10.5152/TurkArchPediatr.2021.20165 |
Ejemplares similares
-
Clinical course of pediatric large vascular anomalies located in the extremities
por: Oktay, Burcu Kılınç, et al.
Publicado: (2021) -
Investigation of 11p15.5 Methylation Defects Associated with Beckwith-Wiedemann Spectrum and Embryonic Tumor Risk in Lateralized Overgrowth Patients
por: Tüysüz, Beyhan, et al.
Publicado: (2023) -
Hemophagocytic Lymphohistiocytosis
por: Kaçar, Ayşe Gonca, et al.
Publicado: (2022) -
A Peculiar Disease in a Young Woman Wanting to Get Pregnant
por: Celkan, Tülin Tiraje, et al.
Publicado: (2021) -
The Clinical and Molecular Spectrum of Trichorhinophalangeal Syndrome Types I and II in a Turkish Cohort Involving 22 Patients
por: Güneş, Nilay, et al.
Publicado: (2023)