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Juvenile hyaline fibromatosis

Index 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). [1]

5 relations: Božidar Puretić, Hereditary gingival fibromatosis, List of cutaneous conditions, List of diseases (J), Nodulosis–arthropathy–osteolysis syndrome.

Božidar Puretić

Božidar Puretić (1921 in Bjelovar – 1971 in Zagreb) was a Croatian physician.

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Hereditary gingival fibromatosis

Hereditary gingival fibromatosis (HGF), also known as idiopathic gingival hyperplasia, is a rare condition of gingival overgrowth.

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List of cutaneous conditions

Many conditions affect the human integumentary system—the organ system covering the entire surface of the body and composed of skin, hair, nails, and related muscle and glands.

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List of diseases (J)

This is a list of diseases starting with the letter "J".

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Nodulosis–arthropathy–osteolysis syndrome

Nodulosis–arthropathy–osteolysis syndrome is a cutaneous condition that shares features with juvenile hyaline fibromatosis.

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Redirects here:

Fibromatosis hyalinica multiplex juvenilis, Murray-Puretic Drescher syndrome, Murray–Puretic–Drescher syndrome.

References

[1] https://en.wikipedia.org/wiki/Juvenile_hyaline_fibromatosis

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