- A Case of Hyaline Fibromatosis Syndrome with a New Variant of Genetic Mutation in ANTXR2 Gene
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Park CS, Lee J, Byun HJ, Lim Y, Park JH, Lee JH, Lee DY, Lee JH, Yang JM, Lee JH, Yoo SY
- KMID: 2456662
- Ann Dermatol.
- 2019 Aug;31(Suppl):S12-S13.
- doi: 10.5021/ad.2019.31.S.S12
No abstract available. -
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- A Case of Hyaline Fibromatosis Syndrome with a New Variant of Genetic Mutation in ANTXR2 Gene
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Park CS, Lee J, Byun HJ, Lim Y, Park JH, Lee JH, Lee DY, Lee JH, Yang JM, Lee JH, Yoo SY
- KMID: 2456635
- Ann Dermatol.
- 2019 Aug;31(Suppl 1):S12-S13.
- doi: 10.5021/ad.2019.31.S.S12
No abstract available. -
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- Juvenile Hyaline Fibromatosis
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Park KT, Chang DY, Sung MW
- KMID: 1460597
- Clin Exp Otorhinolaryngol.
- 2010 Jun;3(2):102-106.
- doi: 10.3342/ceo.2010.3.2.102
Juvenile hyaline fibromatosis (JHF) is a rare, progressive autosomal recessive disease that's characterized by papulonodular skin lesions, soft tissue masses, joint contractures, gingival hypertrophy and osteolytic bone lesions. We present... -
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- Juvenile Hyaline Fibromatosis in an Adult
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Kim YA, Chae SW, Kim CJ, Chi JG
- KMID: 1725668
- Korean J Pathol.
- 2000 Mar;34(3):239-242.
Juvenile hyaline fibromatosis is a rare disorder probably inherited as an autosomal recessive trait. It is characterized by multiple slowly growing subcutaneous nodules, hypertrophy of gingiva, flexion contracture, and radiolucent... -
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