Results 71 to 80 of about 273,607 (146)

Hyaline fibromatosis of Hoffa's fat pad in a patient with a mild type of hyaline fibromatosis syndrome

open access: yes, 2014
Hyaline fibromatosis syndrome (HFS) is a rare, homozygous, autosomal recessive disease, characterized by deposition of hyaline material in skin and other organs, resulting in esthetic problems, disability, and potential life-threatening complications ...
Meuffels, Duncan   +3 more
core   +1 more source

Management of airway obstruction in a severe case of juvenile hyaline fibromatosis

open access: yes, 2005
Juvenile hyaline fibromatosis (JHF) is an extremely rare, genetic disease with unknown etiology. It is characterized by cutaneous nodules and flexural joint contractures, along with hypertrophy of the gingival and oral mucosa, which is probably the most ...
Karabulut, AB   +3 more
core   +1 more source

An Adult with Juvenile Hyaline Fibromatosis of the Foot.

open access: yes, 1994
An unusual consideration in the differential diagnosis of benign, solid tumors of the foot is juvenile hyaline fibromatosis, which only superficially resembles the better known myofibromatosis.
Hallock, Geoffrey G, MD
core   +1 more source

Two siblings with juvenile hyaline fibromatosis: Case reports and review of the literature

open access: yes, 1999
In this paper, we describe two siblings with Juvenile Hyaline Fibromatosis (JE-IF) who were diagnosed at the age of 34 and 29 years respectively. JHF is a very congenital disease, mainly diagnosed, in the first few years of life, with less than 40 ...
Doganavsargil, E   +8 more
core   +1 more source

Juvenile Hyaline Fibromatosis:Impact of Periodontal Care on Quality of Life and a Patient Perspective

open access: yes, 2015
Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive inherited condition presenting early in life and characterized by the accumulation of hyaline-like tissue in the skin as well as various organs.
Yonel, Zehra; id_orcid   +5 more
core   +1 more source

Identification of 2 Novel ANTXR2 Mutations in Patients With Hyaline Fibromatosis Syndrome and Proposal of a Modified Grading System

open access: yes, 2016
Juvenile hyaline fibromatosis (JHF) and infantile systemic hyalinosis (ISH) are rare, autosomal recessive disorders of the connective tissue caused by mutations in the gene encoding the anthrax toxin receptor 2 protein (ANTXR2) located on chromosome 4q21.
Raposo-Amaral, Cesar A.   +10 more
core   +1 more source

Juvenile hyaline fibromatosis: A rare lesion

open access: yesIndian Journal of Pathology and Microbiology, 2011
Yasmin Altaf Momin   +2 more
doaj   +1 more source

Other title: Parent Handbook; Other title: Parent Handbook, Kansas Juvenile Correctional Complex : Guide for Parents; Other title: Guide for Parents

open access: yes, 2011
Revised January 2011; application/pdf"This handbook was designed to provide information to parents, visitors and other interested individuals about the Kansas Juvenile Correctional Complex and its operation."Introduction General Programming ...
Kansas Juvenile Correctional Complex.
core   +1 more source

Juvenile hyaline fibromatosis.

open access: yesJournal of postgraduate medicine, 2005
None
K. C. Nischal   +3 more
openaire   +1 more source

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