Results 41 to 50 of about 625 (116)
Juvenile Hyaline Fibromatosis- A Rare Autosomal Recessive Disease [PDF]
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 +4 more
doaj +1 more source
Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders
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
Aims. Calcifying fibrous tumor (CFT) is a very rare begin fibroblastic tumor featuring a widely anatomical distribution and may mimic various spindle cell tumors. Misdiagnosis and hence mistreatment are likely caused due to unfamiliarity to clinicians or junior pathologists.
Jun Zhou +9 more
wiley +1 more source
Congenital Rhabdomyosarcoma Presenting as a Neck Mass at Birth
Rhabdomyosarcoma is a malignant tumor of the soft tissues which preferentially affects the pediatric population. Neonatal rhabdomyosarcoma is rare, and much of the published literature concerning this entity consists of isolated case reports and small case series.
Leah E. Waldman +4 more
wiley +1 more source
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
Differential dependence on N-glycosylation of anthrax toxin receptors CMG2 and TEM8. [PDF]
ANTXR 1 and 2, also known as TEM8 and CMG2, are two type I membrane proteins, which have been extensively studied for their role as anthrax toxin receptors, but with a still elusive physiological function.
Sarah Friebe +2 more
doaj +1 more source
A Case of Retroperitoneal Castleman’s Disease and an Update on the Latest Evidence
Castleman’s disease is a benign lymphoproliferative condition with three distinct histological subtypes. Clinically it presents in either a unicentric or multicentric manner and can affect various anatomic regions, the mediastinum being the most frequent location.
Eleftherios Spartalis +12 more
wiley +1 more source
The Autosomal Recessive Inheritance of Hereditary Gingival Fibromatosis
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
Orphan Disease: Infantile Systemic Hyalinosis
Infantile systemic hyalinosis — one of the forms of systemic hyaline fibromatosis — is a rare, fatal progressive disease with autosomal recessive inheritance, which is characterized by the accumulation of hyaline substance in different tissues of the ...
Ye.V. Ponochevnaia +6 more
doaj +1 more source
Idiopathic Gingival Fibromatosis Rehabilitation: A Case Report with Two‐Year Followup
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

