Results 21 to 30 of about 273,607 (146)

Juvenile hyaline fibromatosis in one Turkish child

The Turkish Journal of Pediatrics, 2000
We describe a case of juvenile hyaline fibromatosis (JHF) in a Turkish child. Only about 40 cases of juvenile hyaline fibromatosis had been reported in English literature as of March 1998, and it had not been reported in English literature from ...
S Uğraş, N Akpolat, A Metin
doaj   +5 more sources

Juvenile hyaline fibromatosis or infantile systemic hyalinosis: Hyaline fibromatosis syndrome

Indian Journal of Paediatric Dermatology, 2016
Juvenile hyaline fibromatosis or infantile systemic hyalinosis is a rare progressive, fatal autosomal recessive disorder characterized by widespread deposition of hyaline.
K Amrutha Varshini, K Haritha, Chirag A Desai, G Raghurama Rao, A Prasad Chowdary, A Amareswar, P Ramana Murty   +6 more
doaj   +2 more sources

Juvenile Hyaline Fibromatosis- A Rare Autosomal Recessive Disease [PDF]

Journal of Clinical and Diagnostic Research, 2017
Systemic hyalinosis is inherited as an autosomal recessive disease. It may also be referred to as Fibromatosis hyalinica multiplex juvenilis and Murray-Puretic-Drescher syndrome.
PRARTHANA SAMEER KALGAONKAR, MINAL WADE, CHARUSHEELA WARKE, MEENA MAKHECHA, MANISHA KHARE   +4 more
doaj   +2 more sources

Juvenile hyaline fibromatosis in siblings

Indian Journal of Pathology and Microbiology, 2019
Background: Juvenile Hyaline Fibromatosis is a rare autosomal recessive connective tissue disorder. Case Characteristics: Three year old girl with multiple facial nodules, gingival hypertrophy and multiple joint contractures. Her sibling, male child also
Valkodai Ramanathan Ravikumar, Ram Ganesh Veerappan Ramamoorthi, Sivakumar Manisankar   +2 more
doaj   +3 more sources

Juvenile Hyaline Fibromatosis Presenting as Progressive Flexion Contracture of the Middle Finger in a Child: A Case Report [PDF]

Plastic and Reconstructive Surgery, Global Open
Summary:. Juvenile fibromatosis is a rare benign fibroproliferative condition that may cause functional impairment when affecting the upper extremity. Deep involvement of flexor tendons in the hand is particularly unusual.
Simeon Mulugeta Mengistu, MD, Abraham Gebreegziabher Negussie, MD, FCS-ECSA, Yohannis Elias, MD, Harom Gari Wakjira, MD, Tariku Mulatu Bore, MD   +4 more
doaj   +2 more sources

Juvenile Hyaline Fibromatosis (JHF): A Rare Case with Recurrence [PDF]

Journal of Clinical and Diagnostic Research, 2014
Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive disease. Less than 70 cases of JHF have been reported worldwide and extremely few from India.
Rashmi M.V., Geetha J.P., Srinivas Arava, Niranjana Murthy B., Kodandaswamy C.R.   +4 more
doaj   +2 more sources

Hyaline fibromatosis syndrome: A rare inherited disorder

Indian Journal of Dermatology, 2016
Hyaline fibromatosis syndrome (HFS) is rare autosomal recessive disease characterized by the deposition of amorphous hyaline material in skin and visceral organs.
Meeta Dipak Mantri, Mahajan M Pradeep, Patil O Kalpesh, Raj J Pranavsinh   +3 more
doaj   +2 more sources

Juvenile Hyaline Fibromatosis - Child with Scalp Swellings [PDF]

Journal of Liaquat National Hospital
Juvenile hyaline fibromatosis is a recessive autosomal hereditary disorder characterized by abnormal growth of hyalinized fibrous tissue. Its clinical presentation is manifested by benign skin lesions, bone lesions, joint contractures, and gingival ...
Naila Parveen, Javeria Mansoor, Komal Masroor   +2 more
doaj   +3 more sources

Multiple scalp tumors in juvenile hyaline fibromatosis with antxr-2 mutation in a family [PDF]

Indian Journal of Dermatology, 2021
Vibhu Mendiratta, Anuja Yadav, Jyoti Yadav, Smita Singh, Neha Suman   +4 more
doaj   +2 more sources

Juvenile Hyaline Fibromatosis or Hyaline Fibromatosis Syndrome?

Indian Journal of Pathology and Microbiology, 2012
Bhavana Bharambe
doaj   +3 more sources