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| juvenile hyaline fibromatosis ： ウィキペディア英語版 |
juvenile hyaline fibromatosis
Juvenile hyaline fibromatosis (also known as "Fibromatosis hyalinica multiplex juvenilis,"〔 "Murray–Puretic–Drescher syndrome") 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 neurofibromatosis.〔Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). Page 989. McGraw-Hill. ISBN 0-07-138076-0.〕
== See also ==
* List of cutaneous conditions
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