Results 41 to 50 of about 273,607 (146)
Archives of Dermatology, 1976 A boy had multiple large tumors on the scalp, whitish nodules on the nape and both sides of the neck, hypertrophic gingiva, and severe flexural contractures of hip and knee joints. The histopathologic structure of the tumor was characteristic of juvenile hyalin fibromatosis.
O G, Costa, P U, Costa
openaire +4 more sources
Infantile systemic hyalinosis: report of a case from Bahrain and review of literature
Journal of Biochemical and Clinical Genetics, 2020 Background: Infantile systemic hyalinosis (ISH), an allelic form of hyaline fibromatosis syndrome, is a rare fatal autosomal recessive disorder that is caused by mutations in the CMG2/ANTRX2 gene encoding the transmembrane anthrax toxin receptor 2.
Zahra Alsahlawi +4 more
doaj +1 more source
Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders
American Journal of Medical Genetics Part A, Volume 179, Issue 10, Page 1913-1981, October 2019., 2019 Abstract Dental anomalies occur frequently in a number of genetic disorders and act as major signs in diagnosing these disorders. We present definitions of the most common dental signs and propose a classification usable as a diagnostic tool by dentists, clinical geneticists, and other health care providers.
Muriel de La Dure‐Molla +24 more
wiley +1 more source
Case Reports in Pathology, Volume 2019, Issue 1, 2019., 2019 Background. Fibrous hamartoma of infancy is a rare soft tissue lesion of infants and young children with characteristic triphasic morphology. Case Description. An 18‐month‐old female child was presented with complaints of swelling over right leg shin since birth. On examination, a lump of size 7x3 cm was identified which was mobile and nontender. Local
G. Lama +5 more
wiley +1 more source
BioMed Research International, Volume 2018, Issue 1, 2018., 2018 Previous studies have demonstrated associations of ANTXR2 gene polymorphisms with ankylosing spondylitis (AS). These associations differ depending on the ethnic populations and AS subgroups studied. Purposes of the current study were to evaluate the associations of 4 single nucleotide polymorphisms (SNPs) of the ANTXR2 gene with susceptibility to AS ...
Jiayue Hu +9 more
wiley +1 more source
Case Report - Juvenile hyaline fibromatosis in siblings
, 2005 Juvenile hyaline fibromatosis (JHF) is a rare, autosomal recessively inherited disorder. We report two siblings with multiple large tumors on the scalp, translucent papules on the nape of the neck, hypertrophic gingiva, and severe flexural ...
Vinod Jain +5 more
core +2 more sources
BioMed Research International, Volume 2017, Issue 1, 2017., 2017 The purpose of this study was to investigate whether LED light at different wavelengths affects the expression profile of 143 cancer predisposition genes in both diabetic and normal human fibroblasts. In this study, both diabetic and normal fibroblast cell lines were cultured and irradiated with red (635 nm), green (520 nm), and blue (465 nm) LED light
Pongsathorn Chotikasemsri +3 more
wiley +1 more source
The Autosomal Recessive Inheritance of Hereditary Gingival Fibromatosis
Case Reports in Dentistry, Volume 2013, Issue 1, 2013., 2013 Hereditary gingival fibromatosis (HGF) is a rare condition which is marked by enlargement of gingival tissue that covers teeth to various extents leading to aesthetic disfigurement. This study presents a case of a 28‐year‐old female patient and 18‐year‐old male who belong to the same family suffering from HGF with chief complaint of overgrowing ...
Poulami Majumder +7 more
wiley +1 more source
Idiopathic Gingival Fibromatosis Rehabilitation: A Case Report with Two‐Year Followup
Case Reports in Dentistry, Volume 2013, Issue 1, 2013., 2013 Gingival enlargements are quite common and may be either inflammatory, noninflammatory, or a combination of both. Gingival hyperplasia is a bizarre condition causing esthetic, functional, psychological, and masticatory disturbances of the oral cavity. Causes of gingival enlargement can be due to plaque accumulation, due to poor oral hygiene, inadequate
Mahesh Jayachandran +4 more
wiley +1 more source
Idiopathic Gingival Hyperplasia: A Case Report with a 17‐Year Followup
Case Reports in Dentistry, Volume 2011, Issue 1, 2011., 2011 This is a case report of a patient with idiopathic gingival hyperplasia and an undiagnosed genetic disorder that demonstrated static encephalopathy, mental retardation, developmental delay, seizures, hypotonia, and severe gingival hypertrophy. The clinical dental management and attempts to obtain a genetic diagnosis are described.
Bien Lai +3 more
wiley +1 more source