نتایج جستجو برای: jeune syndrome

تعداد نتایج: 622621  

Journal: :Medicina oral, patologia oral y cirugia bucal 2009
Daniela Alves-Pereira Leonardo Berini-Aytés Cosme Gay-Escoda

Ellis-van Creveld syndrome is a genetic disorder that was first described by Richard Ellis and Simon van Creveld in 1940. The four principal characteristics are chondrodysplasia, polydactyly, ectodermal dysplasia and congenital heart defects. The orofacial manifestations include multiple gingivolabial musculofibrous fraenula, dental anomalies, hypodontia and malocclusion. The disease can be dia...

2014
Bruno Drera Daniela Ferrari Pietro Cavalli Carlo Poggiani

KEY CLINICAL MESSAGE We report the case of a premature, very low birth weight, newborn with stigmata of Jeune syndrome, a rare skeletal dysplasia, and marked renal involvement (i.e. remarkable prenatal oligohydramnios, histologic nephronophthisis-like pattern, macroscopic renal cysts, and renal failure), expanding the phenotype consistent with the continuum of syndromic ciliopathies.

Journal: :American journal of medical genetics. Part A 2010
A M Lehman P Eydoux D Doherty I A Glass D Chitayat B Y H Chung S Langlois S L Yong R B Lowry F Hildebrandt P Trnka

Ciliary disorders share typical features, such as polydactyly, renal and biliary cystic dysplasia, and retinitis pigmentosa, which often overlap across diagnostic entities. We report on two siblings of consanguineous parents and two unrelated children, both of unrelated parents, with co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophy, an association that adds to the obs...

2017
Meryem Rchachi Maazou Mahamane Larwanou Hanan El Ouahabi Farida Ajdi

Résumé Les anomalies du développement décrites dans le syndrome de Williams, associent classiquement une dysmorphie, des malformations cardiovasculaires et un profil neuropsychologique particulier et d'autres troubles associés. Nous rapportons le cas d'une jeune fille âgée de 17 ans, issu d'un mariage non consanguin, chez qui le syndrome de Williams a été découvert suite à une exploration dans ...

Journal: :Case Reports in Anesthesiology 2015

2015
Mehmet I. Buget Emine Ozkan Ipek S. Edipoglu Suleyman Kucukay

Jeune syndrome (JS) is an autosomal recessive disease also known as asphyxiating thoracic dystrophy. A narrow bell-shaped thoracic wall and short extremities are the most typical features of the syndrome. Prognosis in JS depends on the severity of the pulmonary hypoplasia caused by the chest wall deformity. Most patient deaths are due to respiratory problems at early ages. Herein, we report a c...

2013
Kerry A. Miller Casey J. Ah-Cann Megan F. Welfare Tiong Y. Tan Kate Pope Georgina Caruana Mary-Louise Freckmann Ravi Savarirayan John F. Bertram Michael S. Dobbie John F. Bateman Peter G. Farlie

Cilia are architecturally complex organelles that protrude from the cell membrane and have signalling, sensory and motility functions that are central to normal tissue development and homeostasis. There are two broad categories of cilia; motile and non-motile, or primary, cilia. The central role of primary cilia in health and disease has become prominent in the past decade with the recognition ...

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