scholarly journals The Learning Disabilities Network (LeaDNet): Using neurofibromatosis type 1 (NF1) as a paradigm for translational research

2012 ◽  
Vol 158A (9) ◽  
pp. 2225-2232 ◽  
Author(s):  
Maria T. Acosta ◽  
Carrie E. Bearden ◽  
Xavier F. Castellanos ◽  
Laurie Cutting ◽  
Ype Elgersma ◽  
...  
Keyword(s):  
Learning Disabilities ◽  
Translational Research ◽  
Neurofibromatosis Type 1 ◽  
Neurofibromatosis Type

scholarly journals Corrigendum to “The Learning Disabilities Network (LeaDNet): Using Neurofibromatosis Type 1 [NF1] as a Paradigm for Translational Research”

2012 ◽  
Vol 161 (1) ◽  
pp. 236-236
Author(s):  
Maria T. Acosta ◽  
Carrie E. Bearden ◽  
Xavier F. Castellanos ◽  
Laurie Cutting ◽  
Ype Elgersma ◽  
...  
Keyword(s):  
Learning Disabilities ◽  
Translational Research ◽  
Neurofibromatosis Type 1 ◽  
Neurofibromatosis Type

Neurofibromatosis Type 1

2017 ◽  
Author(s):  
David S. Wolf
Keyword(s):  
Learning Disabilities ◽  
Neurofibromatosis Type 1 ◽  
Autosomal Dominant ◽  
Neurofibromatosis Type ◽  
Vascular Abnormalities ◽  
Hyperactivity Disorder ◽  
Café Au Lait Spots ◽  
Lisch Nodules ◽  
Neurocutaneous Disorder

Neurofibromatosis type 1 is a common, autosomal dominant, monogenetic neurocutaneous disorder. It is characterized by café au lait spots, axillary and inguinal freckling, Lisch nodules, optic pathway gliomas, neurofibromas, and distinctive bony abnormalities. Also associated with this condition are other central nervous system tumors, scoliosis, hypertension, vascular abnormalities, and cognitive issues such as learning disabilities and attention deficit-hyperactivity disorder.

Brain white matter structures in Learning Disabilities in Neurofibromatosis type 1

2016 ◽  
Vol 108 ◽  
pp. 172
Author(s):  
Nadir Díaz-Simón ◽  
Nancy Estévez-Pérez ◽  
Daylín Góngora-Lleonart ◽  
Maydel Fernandez-Alonso ◽  
Vivian Reigosa-Crespo ◽  
...  
Keyword(s):  
Learning Disabilities ◽  
White Matter ◽  
Neurofibromatosis Type 1 ◽  
Neurofibromatosis Type ◽  
Brain White Matter

scholarly journals Legius Syndrome in a 13 Month Old Boy: A Case Report

2017 ◽  
Vol 2 (1) ◽  
Keyword(s):  
Learning Disabilities ◽  
Case Report ◽  
Developmental Delay ◽  
Neurofibromatosis Type 1 ◽  
Autosomal Dominant ◽  
Clinical Manifestations ◽  
Neurofibromatosis Type ◽  
Café Au Lait Spots ◽  
Legius Syndrome

Legius syndrome is autosomal dominant and caused by mutations in the SPRED1 gene. Clinical manifestations include multiple cafe-au-lait spots, axillary/ inguinal freckling and a degree of macrocephaly, without the non-pigmentary signs of neurofibromatosis type 1 (NF1). Learning disabilities, developmental delay and ADHD are also known.

Cognitive Profile of Neurofibromatosis Type 1: Rethinking Nonverbal Learning Disabilities

2004 ◽  
Vol 19 (3) ◽  
pp. 155-165 ◽  
Author(s):  
Laurie E. Cutting ◽  
Amy M. Clements ◽  
Andrea D. Lightman ◽  
Pamula D. Yerby-Hammack ◽  
Martha Bridge Denckla
Keyword(s):  
Learning Disabilities ◽  
Neurofibromatosis Type 1 ◽  
Neurofibromatosis Type ◽  
Cognitive Profile ◽  
Nonverbal Learning Disabilities ◽  
Nonverbal Learning
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