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Juvenile hyaline fibromatosis

juvenile hyaline fibromatosis, juvenile hyaline fibromatosis pathology
Juvenile hyaline fibromatosis also known as "Fibromatosis hyalinica multiplex juvenilis,"1 "Murray–Puretic–Drescher syndrome"1 is a very rare, autosomal recessive disease due to mutations in capillary morphogenesis protein-2 CMG-2 gene It occurs from early childhood to adulthood, and presents as slow-growing, pearly white or skin-colored dermal or subcutaneous papules or nodules on the face, scalp, and back, which may be confused clinically with neurofibromatosis2

See alsoedit

  • List of cutaneous conditions

Referencesedit

  1. ^ a b Rapini, Ronald P; Bolognia, Jean L; Jorizzo, Joseph L 2007 Dermatology: 2-Volume Set St Louis: Mosby ISBN 1-4160-2999-0 
  2. ^ Freedberg, et al 2003 Fitzpatrick's Dermatology in General Medicine 6th ed Page 989 McGraw-Hill ISBN 0-07-138076-0


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Juvenile hyaline fibromatosis


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    29.10.2014


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