Nodulosis–arthropathy–osteolysis syndrome is a cutaneous condition that shares features with juvenile hyaline fibromatosis.[1]
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Winchester syndrome — in a rare congenital connective tissue disease described in 1969,cite journal |author=Winchester P, Grossman H, Lim WN, Danes BS |title=A new acid mucopolysaccharidosis with skeletal deformities simulating rheumatoid arthritis |journal=Am J… … Wikipedia
List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… … Wikipedia
Coarse facial features — refer to a similar change in facial features in the advanced stage of certain conditions like Cretinism, Mucopolysaccharidoses etc, where affected individuals look remarkably similar due to the coarsening of their facial features. These typical… … Wikipedia
MMP2 — Matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase), also known as MMP2, is a human gene. PBB Summary section title = summary text = Proteins of the matrix metalloproteinase (MMP) family are involved in the… … Wikipedia
