Results 111 to 120 of about 273,607 (146)
Eyelid tumour and juvenile hyaline fibromatosis
Journal of Plastic, Reconstructive and Aesthetic Surgery, 2005 We report the case of a 2-year-old boy suffering from juvenile hyaline fibromatosis. Our patient had all the main clinical features of the disease, i.e.
A de Mey
exaly +2 more sources
Hyaline fibromatosis syndrome (juvenile hyaline fibromatosis): whole-body MR findings in two siblings with different subcutaneous nodules distribution [PDF]
Skeletal Radiology, 2017 : Hyaline fibromatosis syndrome (juvenile hyaline fibromatosis) is a rare, progressive, autosomal recessive disorder whose main hallmark is the deposition of amorphous hyaline material in soft tissues, with an evolutionary course and health impairment ...
Dario Picone +2 more
exaly +2 more sources
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Pediatric Dermatology, 2001
Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive disease with onset in infancy or early childhood. It is characterized by papulonodular skin lesions, soft tissue masses, gingival hypertrophy, and flexion contractures of the large joints. The light and electron microscopic features are very distinctive. Here we report an 8‐month‐old boy
M, Larralde +3 more
openaire +3 more sources
Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive disease with onset in infancy or early childhood. It is characterized by papulonodular skin lesions, soft tissue masses, gingival hypertrophy, and flexion contractures of the large joints. The light and electron microscopic features are very distinctive. Here we report an 8‐month‐old boy
M, Larralde +3 more
openaire +3 more sources
Periodontal treatment of two siblings with juvenile hyaline fibromatosis
Journal of Clinical Periodontology, 2005 Background and Aim: Juvenile hyaline fibromatosis (JHF) is an autosomal recessive disease that presents with multiple subcutaneous nodular tumours, gingival fibromatosis, flexion contractures of the joint and hyaline material accumulation in ...
Sema Hakki +2 more
exaly +2 more sources
The British Journal of Radiology, 1981
A case of juvenile hyaline fibromatosis in a ten-year-old Asian girl is presented. This autosomal recessively inherited condition has not previously been described in the radiological literature. This patient demonstrates well the characteristic radiological appearance.
D A, Stringer, C M, Hall
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A case of juvenile hyaline fibromatosis in a ten-year-old Asian girl is presented. This autosomal recessively inherited condition has not previously been described in the radiological literature. This patient demonstrates well the characteristic radiological appearance.
D A, Stringer, C M, Hall
openaire +2 more sources
Journal of Pediatric Orthopaedics B, 1998
The authors present a 9-year-old girl with a juvenile hyaline fibromatosis observed before any treatment and after surgical releases. The disorder showed impressive clinical features both concerning the size of the dermal nodules and the degree of limitation of involved joints.
A, Nunziata Rega +6 more
openaire +4 more sources
The authors present a 9-year-old girl with a juvenile hyaline fibromatosis observed before any treatment and after surgical releases. The disorder showed impressive clinical features both concerning the size of the dermal nodules and the degree of limitation of involved joints.
A, Nunziata Rega +6 more
openaire +4 more sources
British Journal of Dermatology, 1983
SUMMARY A 4-year-old boy with juvenile hyaline fibromatosis (systemic hyalinosis) is described. The clinical features, pathology and prognosis of this condition are discussed.
A Y, Finlay, S D, Ferguson, P J, Holt
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SUMMARY A 4-year-old boy with juvenile hyaline fibromatosis (systemic hyalinosis) is described. The clinical features, pathology and prognosis of this condition are discussed.
A Y, Finlay, S D, Ferguson, P J, Holt
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Juvenile non‐hyaline fibromatosis: juvenile hyaline fibromatosis without prominent hyaline changes
Journal of Cutaneous Pathology, 2005Abstract: Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive disease of the connective tissue. It is characterized by papulonodular skin lesions, soft tissue masses, gingival hypertrophy, osteolytic bone lesions and flexion contractures of the large joints.
Rana Yavuzer, Anadolu +3 more
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Anesthesiology, 1990
Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive disease with incomplete penetrance. Difficulty with intubation of the trachea may be caused by gingival hypertrophy and tempromandibular joint and cervical spine ...
G C, Vaughn +3 more
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Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive disease with incomplete penetrance. Difficulty with intubation of the trachea may be caused by gingival hypertrophy and tempromandibular joint and cervical spine ...
G C, Vaughn +3 more
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Der Hautarzt, 1997
Juvenile hyaline fibromatosis is a rare autosomal recessive connective tissue disease first described in 1873 by Murray. Major diagnostic criteria are multiple cutaneous tumors and gingival hypertrophy; minor criteria include contractures, osteolytic lesions and a positive family history.
M, Schaller +3 more
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Juvenile hyaline fibromatosis is a rare autosomal recessive connective tissue disease first described in 1873 by Murray. Major diagnostic criteria are multiple cutaneous tumors and gingival hypertrophy; minor criteria include contractures, osteolytic lesions and a positive family history.
M, Schaller +3 more
openaire +2 more sources