Neurofibromatosis Type 1 Complicated by Atypical Coarctation of the Thoracic Aorta

Neurofibromatosis type 1 (NF1) is a relatively common autosomal dominant genetic disorder with a prevalence of 1 in 3,000 (0.03%) at birth. Clinical features are café-au-lait macules, intertriginous freckling, dermal neurofibroma, iris hamartoma (Lisch nodules), and learning disability. NF1 vasculop...

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Hlavní autoři: Kimura, Masato, Kakizaki, Shuhei, Kawano, Kengo, Sato, Shinichi, Kure, Shigeo
Médium: Artigo
Jazyk:Inglês
Vydáno: Hindawi Publishing Corporation 2013
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3603612/
https://ncbi.nlm.nih.gov/pubmed/23533898
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/458543
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