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DDx

Discussion in 'Spot Diagnosis' started by J.P.C. Peper, Jun 22, 2012.

  1. J.P.C. Peper

    J.P.C. Peper Bronze Member

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    What's your diagnosis?

    I'll post the correct answer in a few days!

    DDx.jpg
     

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  2. lakmalDJ

    lakmalDJ Famous Member

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    Neurofibromatosis type 1
     

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    Walkov Famous Member

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    neurofibromatosisi -morbus Reklinghausen!
     

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    ghazala Well-Known Member

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    madhubhashini Famous Member

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    Gospodin Seki Moderator Staff Member

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    dupuytren Bronze Member

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    neurofibromatosis
     

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    Aman Setiya Bronze Member

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    Rocket Queen Super Moderator

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  10. J.P.C. Peper

    J.P.C. Peper Bronze Member

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    Correct answer:

    Neurofibromatosis (type 2).

    It's also known as MISME-syndrome; Multiple Inherited Schwannomas, Meningeomas and Ependymomas. In this case, the patient is covered in neurofibromas in the skin. It's a genetic (autosomal dominant) disease, caused by mutations in the Merlin-gene.
     

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