Results 101 to 110 of about 20,731 (178)

Clinical manifestations and oral findings in fraser syndrome

, 2007
This article is the first known case report of Fraser syndrome in the dental literature. Its purpose was to present the clinical manifestations, oral findings, and dental treatment of a 14-year, 10-month-old female patient.
Diniz, Michele Baffi, Lima, Luciana Monti, De Paula, Andréia Bolzan, Santos-Pinto, Lourdes Aparecida Martins dos, Sacono, Nancy Tomoko   +4 more
core   +1 more source

Prenatal diagnosis of Fraser syndrome caused by novel variants of FREM2. [PDF]

Hum Genome Var, 2020
Ikeda S, Akamatsu C, Ijuin A, Nagashima A, Sasaki M, Mochizuki A, Nagase H, Enomoto Y, Kuroda Y, Kurosawa K, Ishikawa H.   +10 more
europepmc   +1 more source

Fraser Syndrome: case report in lacrimal system

, 2014
Fraser syndrome is a systemic condition characterized by cryptophthalmos, syndactyly and abnormal genitalia, which may be associated with urinary tract, ear, nose, larynx and skeletal abnormalities.
Lorena, Silvia Helena Tavares, Eliana Domingues Gonçalves, Cláudio Enrique Cuadros Jablinski, Machado, Marco Antonio de Campos [UNIFESP], César Augusto Briceño, Gonçalves, Eliana Domingues, Silva, João Amaro Ferrari, Marco Antônio Campos Machado, Silvia Helena Tavares Lorena, João Amaro Ferrari Silva, Briceño, César Augusto, Jablinski, Cláudio Enrique Cuadros   +11 more
core   +1 more source

Prediction the Quality of Life based on the Perception of Suffering, the Meaning of Life, Social Support and Psychological Flexibility in Irritable Bowel Syndrome Patient [PDF]

Taḥqīqāt-i ̒Ulūm-i Raftārī
Aim and Background: The present study aimed to predict the quality of life based on the perception of suffering, meaning of life, social support, and psychological flexibility in irritable bowel syndrome patients and by a correlational descriptive method.
shila Shahbazi Bandani, Seyed Hamid Atashpour   +1 more
doaj  

Genetic mutation of Frem3 does not causeFraser syndrome in mice. [PDF]

Exp Anim, 2020
Kiyozumi D, Mori M, Kodani M, Ikawa M.
europepmc   +1 more source

Melnick-Fraser Syndrome [PDF]

Dermatology, 2009
V. Torres-Peris, E. Jorda, D. Ramon, J. Peiro, A. Revert, T. Torres-Larrosa   +5 more
openaire   +1 more source

Congenital High Airway Obstruction Syndrome (CHAOS) as part of Fraser syndrome: ultrasound and autopsy findings

, 2013
Congenital High Airway Obstruction Syndrome (CHAOS) is a potential lethal condition. We describe a case report of CHAOS, with additional malformations diagnosed at 20 weeks.
Peeters, Hilde, Van Robaeys, J., Witters, Ingrid, Fryns, Jean-Pierre, Mesens, Tinne   +4 more
core  

Mutations in GRIP1 Cause Fraser Syndrome

, 2012
Background: Fraser syndrome (FS) is a autosomal recessive malformation syndrome characterised by cryptophthalmos, syndactyly and urogenital defects. FS is a genetically heterogeneous condition.
van Zon, Patrick, Blair, Edward, Ploos van Amstel, Hans Kristian, Kariminejad, Ariana, Schanze, Denny, Vogel, Maartje J., Cox, Philip, Zenker, Martin, Ghaderi-Sohi, Siavash, Brueton, Louise, Gijzen, Marleen, van Tuil, Marc, Scambler, Peter J., van Haelst, MM   +13 more
core  

Fraser Syndrome in a Newborn: Diagnostic Challenges Based on Clinical Criteria. [PDF]

Cureus
Ettoini K, Mesbah K, Elboussaadni Y, Oulmaati A.   +3 more
europepmc   +1 more source

Prenatal Diagnosis of Fraser Syndrome at 20 Weeks' Gestation: A Case Report and Review of Literature. [PDF]

Cureus
Rana S.
europepmc   +1 more source