نتایج جستجو برای: van creveld syndrome

تعداد نتایج: 686722  

Journal: :Journal of Pharmacy and Bioallied Sciences 2012

Journal: :Taiwanese Journal of Obstetrics and Gynecology 2012

Journal: :American journal of medical genetics. Part C, Seminars in medical genetics 2009
Victor L Ruiz-Perez Judith A Goodship

Ellis-van Creveld syndrome (EvC; OMIM 225500) is a recessive disorder comprising chondrodysplasia, polydactyly, nail dysplasia, orofacial abnormalities and, in a proportion of patients, cardiovascular malformations. Weyers acrodental dysostosis (Weyers; OMIM 193530) is an allelic dominant disorder comprising polydactyly, nail dysplasia, and orofacial abnormalities. EvC results from loss-of-func...

Journal: :Journal of advances in medical and biomedical research 2023

Journal: :Folia morphologica 2011
M R Sangam S S Sarada Devi K Krupadanam K Anasuya

Cor triloculare biventriculare is a rare congenital malformation of the heart in which there is a complete absence of the atrial septum. It is usually associated with other anomalies like complete atrioventricular canal defect, polysplenic syndrome, isolated dextrocardia, Ellis-van Creveld syndrome, or persistent left superior vena cava. We report a case of a stillborn male foetus of 35 weeks g...

Journal: :Kathmandu University medical journal 2008
M M Shenoy K Gopa B S Girisha J Pinto V Shetty

Two male siblings aged 12 and 15 years (Figure 1) presented with growth retardation, limb abnormalities and, defective teeth and nail since childhood. There was no history of similar defects in other family members. On examination their height was 114 cm and 130 cm (expected height; 169 cm and 150 cm) respectively. There were hypoplastic and dystrophic nails, and microdontia and hypodontia on d...

2016
Honghao Zhang Nobuhiro Kamiya Takehito Tsuji Haruko Takeda Greg Scott Sudha Rajderkar Manas K Ray Yoshiyuki Mochida Benjamin Allen Veronique Lefebvre Irene H Hung David M Ornitz Tetsuo Kunieda Yuji Mishina

Ellis-van Creveld (EvC) syndrome is a skeletal dysplasia, characterized by short limbs, postaxial polydactyly, and dental abnormalities. EvC syndrome is also categorized as a ciliopathy because of ciliary localization of proteins encoded by the two causative genes, EVC and EVC2 (aka LIMBIN). While recent studies demonstrated important roles for EVC/EVC2 in Hedgehog signaling, there is still lit...

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