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Results 1 - 9 of 9 for "Café-au-lait" macules with pulmonary stenosis
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  1. Neurofibromatosis-1 
    Neurofibromatosis-1 (NF1) is an inherited disorder in which nerve tissue tumors (neurofibromas) form in the: Upper and ...
    https://medlineplus.gov/ency/article/000847.htm - Medical Encyclopedia
  2. ClinicalTrials.gov: Neurofibromatosis 1 From the National Institutes of Health (National Institutes of Health)  
    Neurofibromatosis/Clinical Trials ... Neurofibromatosis ... National Institutes of Health ... From the National Institutes of Health
    https://clinicaltrials.gov/...romatosis+1"&aggFilters=status:not rec - External Health Links
  3. NF1 gene 
    ... 3. Citation on PubMed Dasgupta B, Gutmann DH. Neurofibromatosis 1: closing the GAP between mice and men. Curr ... B, Fahsold R, Mautner VF. NF1 mutations in neurofibromatosis 1 patients with plexiform neurofibromas. Hum Mutat. 2002 Mar; ...
    https://medlineplus.gov/genetics/gene/nf1 - Genetics
  4. Neurofibromatosis type 1 
    ... develops the tumors characteristic of neurofibromatosis type 1. Neurofibromatosis 1 NF1 Peripheral neurofibromatosis Recklinghausen disease, nerve Von Recklinghausen ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
  5. Neurofibromatosis (National Library of Medicine)  
    Neurofibromatosis is a genetic disorder of the nervous system. It mainly affects how nerve cells form and grow. It causes tumors to grow on nerves. You can get neurofibromatosis ...
    https://medlineplus.gov/neurofibromatosis.html - Health Topics
  6. Pheochromocytoma (Mayo Foundation for Medical Education and Research)  
    Pheochromocytoma/Start Here ... Pheochromocytoma ... Mayo Foundation for Medical Education and Research
    https://www.mayoclinic.org/.../symptoms-causes/syc-20355367?p=1 - External Health Links
  7. Legius syndrome 
    ... loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype. Nat Genet. 2007 Sep;39(9): ...
    https://medlineplus.gov/genetics/condition/legius-syndrome - Genetics
  8. SPRED1 gene 
    ... loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype. Nat Genet. 2007 Sep;39(9): ...
    https://medlineplus.gov/genetics/gene/spred1 - Genetics
  9. Frequently Asked Questions about NF (Children's Tumor Foundation) - PDF  
    Neurofibromatosis/Start Here ... Neurofibromatosis ... Children's Tumor Foundation ... PDF
    https://www.ctf.org/.../uploads/2023/12/CTF_QandA_Brochure.pdf - External Health Links